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        <title>Biochimie via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Biochimie' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Biochimie&t=Biochimie&s=Search&f=source]]></link>
        <lastBuildDate>Sun, 21 Mar 2010 16:57:38 +0100</lastBuildDate>
        <item>
            <title>A structure-activity study to identify novel and efficient substrates of the human semicarbazide-sensitive amine oxidase/VAP-1 enzyme.</title>
            <link>http://www.medworm.com/index.php?rid=3385978&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20298739%26dopt%3DAbstract</link>
            <description>Authors: Bonaiuto E, Lunelli M, Scarpa M, Vettor R, Milan G, Di Paolo ML
    Kinetic studies were performed with various alkanamines as &quot;substrate probes&quot; of the properties of the active site of the human semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1). We found that the enzyme-substrate recognition step is mainly controlled by apolar interactions and that a &quot;good&quot; substrate has a molecular structure containing a long aliphatic chain and a second positive charge at a distance greater than 12 A from the reactive amino group. In this context, we identified a novel substrate for the human SSAO/VAP-1, 1,12-diaminododecane (DIADO), which is characterised by the highest catalytic efficiency reported to date in comparison to the prototypic substrate benzylamine. Com...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385978</comments>
            <pubDate>Mon, 15 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Fatty Acid Desaturase 3 (Fads3) is a singular member of the Fads cluster.</title>
            <link>http://www.medworm.com/index.php?rid=3370986&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226833%26dopt%3DAbstract</link>
            <description>Authors: Blanchard H, Legrand P, P&amp;#xE9;drono F
    Since its identification in 2000, no function has been attributed to the Fatty Acid Desaturase 3 (Fads3) gene. This gene is located within the Fads cluster, which also contains Fads1 and Fads2, coding respectively for the 5- and 6- desaturases. Based on the sequence homology between these three genes, Fads3 may be a new fatty acid desaturase. It is thus essential to understand its involvement in Polyunsaturated Fatty Acid (PUFA) biosynthesis in order to improve our knowledge on lipid metabolism. Gene expression studies provided evidences on the specificity of Fads3 compared to Fads1 and Fads2, concerning the tissue distribution, alternative splicing and regulation. These works also identified possible physiological functions in which Fads...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3370986</comments>
            <pubDate>Wed, 10 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Snake venoms as a source of compounds modulating sperm physiology: secreted phospholipases A(2) from Oxyuranus scutellatus scutellatus impact sperm motility, acrosome reaction and in vitro fertilization in mice.</title>
            <link>http://www.medworm.com/index.php?rid=3370985&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226834%26dopt%3DAbstract</link>
            <description>Authors: Escoffier J, Couvet M, de Pomyers H, Ray PF, S&amp;#xE8;ve M, Lambeau G, De Waard M, Arnoult C
    The goal of this study was to identify new compounds from venoms able to modulate sperm physiology and more particularly sperm motility. For this purpose, we screened the effects of 16 snake venoms cleared of molecules higher than 15kDa on sperm motility. Venoms rich in neurotoxins like those from Oxyuranus scutellatus scutellatus or Daboia russellii, were highly potent inhibitors of sperm motility. In contrast, venoms rich in myotoxins like those from Echis carinatus, Bothrops alternatus and Macrovipera lebetina, were inactive. From the main pharmacologically-active fraction of the Taipan snake Oxyuranus scutellatus s., a proteomic approach allowed us to identify 16 different proteins, ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3370985</comments>
            <pubDate>Wed, 10 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Localization and function of cytosolic phospholipase A(2)alpha at the Golgi.</title>
            <link>http://www.medworm.com/index.php?rid=3370987&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226226%26dopt%3DAbstract</link>
            <description>Authors: Leslie CC, Gangelhoff TA, Gelb MH
    Cytosolic phospholipase A(2)alpha (cPLA(2)alpha, Group IVA phospholipase A(2)) is a central mediator of arachidonate release from cellular phospholipids for the biosynthesis of eicosanoids. cPLA(2)alpha translocates to intracellular membranes including the Golgi in response to a rise in intracellular calcium level. The enzyme's calcium-dependent phospholipid-binding C2 domain provides the targeting specificity for cPLA(2)alpha translocation to the Golgi. However, other features of cPLA(2)alpha regulation are incompletely understood such as the role of phosphorylation of serine residues in the catalytic domain and the function of basic residues in the cPLA(2)alpha C2 and catalytic domains that are proposed to interact with anionic phospholipids...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3370987</comments>
            <pubDate>Tue, 09 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Functional Dendritic Polymer Architectures as Stimuli Responsive Nanocarriers.</title>
            <link>http://www.medworm.com/index.php?rid=3354659&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20211678%26dopt%3DAbstract</link>
            <description>Authors: Calder&amp;#xF3;n M, Quadir MA, Strumia M, Haag R
    Stimuli responsive polymer architectures are molecular systems which evolve with an external signal. The observed changes are mainly decomposition, isomerization, polymerization, activation, supramolecular aggregation, and structural modifications of these molecules. The external stimuli, which can be combined in order to provoke these molecular changes, are numerous. In this review, we have chosen to present an overview on different mechanisms to impart responsiveness to dendritic polymers, with the particular aim of delivery and release of bioactive molecules.
    PMID: 20211678 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3354659</comments>
            <pubDate>Thu, 04 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Analysis of bacterial RNase P RNA and protein interaction by a magnetic biosensor technique.</title>
            <link>http://www.medworm.com/index.php?rid=3354658&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20211679%26dopt%3DAbstract</link>
            <description>Authors: Li D, Meyer MH, Willkomm DK, Keusgen M, Hartmann RK
    A magnetic sensor technique was applied to analyze the interaction of immobilized bacterial RNase P protein and 3'-biotinylated RNase P RNA bound to streptavidin-coated magnetic beads. Our measurements with three types of beads from different suppliers resulted in K(d)-values of about 1 to 2 nM (at 4.5 mM Mg(2+) and 150 mM NH(4)(+)) for E. coli RNase P RNA and protein, consistent with previous analyses using different techniques. We further measured affinity of the E. coli RNase P protein to chimeric RNase P RNA variants, consisting of an E. coli specificity domain and an engineered archaeal catalytic domain. A &quot;bacterial-like&quot; 1-bp insertion and 2-nt deletion in the helix P2/P3 region largely improved affinity, providing ind...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3354658</comments>
            <pubDate>Thu, 04 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>A C-terminal hydrophobic, solvent-protected core and a flexible N-terminus are potentially required for human papillomavirus 18 E7 protein functionality.</title>
            <link>http://www.medworm.com/index.php?rid=3354657&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20211680%26dopt%3DAbstract</link>
            <description>Authors: Liu S, Tian Y, Greenaway FT, Sun MZ
    The oncogenic potential of the high-risk human papillomavirus (HPV) relies on the expression of genes specifying the E7 and E6 proteins. To investigate further the variation in oligomeric structure that has been reported for different E7 proteins, an HPV-18 E7 cloned from a Hispanic woman with cervical intraepithelial neoplasia was purified to homogeneity most probably as a stable monomeric protein in aqueous solution. We determined that one zinc ion is present per HPV-18 E7 monomer by amino acid and inductively coupled plasma-atomic emission spectroscopy analysis. Intrinsic fluorescence and circular dichroism spectroscopic results indicate that the zinc ion is important for the correct folding and thermal stability of HPV-18 E7. Hydroxyl ra...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3354657</comments>
            <pubDate>Thu, 04 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Structure -activity relationships of new 4-hydroxy- bis-coumarins as radical scavengers and chain-breaking antioxidants.</title>
            <link>http://www.medworm.com/index.php?rid=3354656&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20211681%26dopt%3DAbstract</link>
            <description>Authors: Kancheva VD, Boranova PV, Nechev JT, Manolov II
    The main antioxidant properties of five new 4-hydroxy-bis-coumarins during bulk lipid autoxidation at 80 degrees C and 0.1 mM and 1.0 mM concentrations were studied and compared with 4-hydroxy-2H-chromen-2-one (1). These compounds are: 3,3'-((3,4-dihydroxy-phenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (2), 3,3'-((3,4-dimethoxyphenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (3), 3,3'-((4-hydroxy-3,5-dimethoxy-phenyl) methylene) bis(4-hydroxy-2H-chromen-2-one) (4) 3,3'-((3,4,5- trimethoxyphenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (5) 3,3'-((4-hydroxy-3-methoxy-5-nitrophenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (6), It was found that compound 2 with a catecholic structure in the aromatic nucleus showed the...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3354656</comments>
            <pubDate>Thu, 04 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Electrostatic interactions play a significant role in the affinity of Saccharomyces cerevisiae phosphoenolpyruvate carboxykinase for Mn(2+).</title>
            <link>http://www.medworm.com/index.php?rid=3354655&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20211682%26dopt%3DAbstract</link>
            <description>Authors: Sep&amp;#xFA;lveda C, Poch A, Espinoza R, Cardemil E
    Phosphoenolpyruvate (PEP) carboxykinases catalyse the reversible formation of oxaloacetate (OAA) and ATP (or GTP) from PEP, ADP (or GDP) and CO(2). They are activated by Mn(2+), a metal ion that coordinates to the protein through the epsilon-amino group of a lysine residue, the N(epsilon-2)-imidazole of a histidine residue, and the carboxylate from an aspartic acid residue. Neutrality in the epsilon-amino group of Lys213 of Saccharomyces cerevisiae PEP carboxykinase is expected to be favoured by the vicinity of ionised Lys212. Glu272 and Glu284, located close to Lys212, should, in turn, electrostatically stabilise its positive charge and hence assist in keeping the epsilon-amino group of Lys213 in a neutral state. The mutations ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3354655</comments>
            <pubDate>Thu, 04 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Eukaryote-specific motif of ribosomal protein S15 neighbors A site codon during elongation and termination of translation.</title>
            <link>http://www.medworm.com/index.php?rid=3347088&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20206660%26dopt%3DAbstract</link>
            <description>Authors: Khairulina J, Graifer D, Bulygin K, Ven'yaminova A, Frolova L, Karpova G
    The eukaryotic ribosomal protein S15 is a key component of the decoding site in contrast to its prokaryotic counterpart, S19p, which is located away from the mRNA binding track on the ribosome. Here, we determined the oligopeptide of S15 neighboring the A site mRNA codon on the human 80S ribosome with the use of mRNA analogues bearing perfluorophenyl azide-modified nucleotides in the sense or stop codon targeted to the 80S ribosomal A site. The protein was cross-linked to mRNA analogues in specific ribosomal complexes that were obtained in the presence of eRF1 in the experiments with mRNAs bearing stop codon. Digestion of modified S15 with various specific proteolytic agents followed by identification of ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3347088</comments>
            <pubDate>Wed, 03 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Linking long-term toxicity of xeno-chemicals with short-term biological adaptation.</title>
            <link>http://www.medworm.com/index.php?rid=3318973&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188785%26dopt%3DAbstract</link>
            <description>Authors: Barouki R
    Understanding the mechanisms of long-term toxicities of chemicals is challenging. The present review discusses evidence suggesting that the biological adaptation to acute xenobiotic exposure could lead in the long run to toxic side effects. Upon acute exposure, hydrophobic xenobiotics are sequestered in the adipose tissue, which consequently protects other organs. However, this could also lead to the persistence of these xenochemicals and to a chronic low level internal exposure. The intrinsic properties of the xenobiotic detection and metabolism systems could also account for long-term toxicity. Indeed, hydrophobic xenochemicals are metabolized into more hydrophilic compounds; the first step of this pathway consists in the &quot;activation&quot; of the parent compound into a ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318973</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Resveratrol modulates adipokine expression and improves insulin sensitivity in adipocytes: relative to inhibition of inflammatory responses.</title>
            <link>http://www.medworm.com/index.php?rid=3318972&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188786%26dopt%3DAbstract</link>
            <description>This study aims at evaluating the effects of resveratrol on inflammation-related adipokines expression and insulin sensitivity in adipocytes. We stimulated RAW264.7 cells with LPS and collected the supernatant as a conditioned-medium (CM) for the culture of adipocytes. Resveratrol, at concentrations ranging from 0.1 to 10 muM, effectively inhibited lipopolysaccharide (LPS) -induced TNF-alpha and IL-6 production with the downregulation of relative genes expression in macrophages. Exposing differentiated 3T3-L1 cells to RAW264.7 CM resulted in gene over-expressions of TNF-alpha, IL-6 and resistin, however, mRNA expression of adiponectin and PPARgamma were down-regulated. Pretreatment of CM from resveratrol-treated macropahges reduced the elevated levels of TNF-alpha and IL-6, and significant...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318972</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Characterization of a unique proline iminopeptidase from white-rot basidiomycetes Phanerochaete chrysosporium.</title>
            <link>http://www.medworm.com/index.php?rid=3318971&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188787%26dopt%3DAbstract</link>
            <description>Authors: Li N, Wu JM, Zhang LF, Zhang YZ, Feng H
    A putative gene encoding proline iminopeptidase (PchPiPA) was cloned from Phanerochaete chrysosporium BKM-F-1767 by RT-PCR and expressed successfully in Escherichia coli. The cDNA is 942bp in length and encodes 313 amino acids. The recombinant enzyme was only able to hydrolyze Pro-pNA among the tested synthetic substrates. There is no activity detected toward Leu-pNA, Phe-pNA and Tyr-pNA, as well as GGG-pNA, SGR-pNA, AAV-pNA, AAPL-pNA, AAVA-pNA. And the recombinant enzyme could cleave the peptides derived from enzyme-hydrolytic natural proteins to release free lysine, which was confirmed using synthetic oligopeptides with lysine at N termini as substrate. The optimal pH and temperature for this enzyme were 8.0 and 45 degrees C, respectiv...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318971</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Amino acid regulation of mammalian gene expression in the intestine.</title>
            <link>http://www.medworm.com/index.php?rid=3318970&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188788%26dopt%3DAbstract</link>
            <description>Authors: Brasse-Lagnel CG, Lavoinne AM, Husson AS
    Some amino acids exert a wide range of regulatory effects on gene expression via the activation of different signalling pathways and transcription factors, and a number of cis elements were shown to respond to changes in amino acid concentration. Particular attention has been paid to the effects of glutamine and arginine, which modulate a number of cell functions through the activation of various pathways in different tissues. In the intestine, appropriate concentrations of both arginine and/or glutamine contribute to facilitate cell proliferation, to limit the inflammatory response and apoptosis, and to modulate intermediary metabolism through specific transcription factors. Particularly, besides its role as a major fuel for enterocyte...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318970</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>A fibrinogenolytic proteinase Purification and characterization of a fibrinogenolytic and hemorrhagic metalloproteinase isolated from Vipera lebetina venom.</title>
            <link>http://www.medworm.com/index.php?rid=3318969&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188789%26dopt%3DAbstract</link>
            <description>Authors: Hamza L, Gargioli C, Castelli S, Rufini S, Laraba-Djebari F
    Serious clinical problems such as hemorrhage, edema and tissue necrosis are observed following viperid envenoming. A proteinase (VLH2) was isolated from Vipera lebetina by combination of two chromatographic steps of gel filtration on Sephadex G-75 followed by DEAE Sephadex A-50. This acidic proteinase, with a molecular mass of about 55kDa and isoelectric point of 5.4, displayed a fibrinogenolytic and hemorrhagic activities. VLH2 hydrolyses rapidly the Aalpha-chain of fibrinogen, followed, more slowly, by the Bbeta-chain, leaving the gamma-chain unaffected. The proteolytic and hemorrhagic activities of VLH2 were inhibited by EDTA, EGTA and 1-10 phenanthroline. However, these activities were not affected by AEBSF, Aprot...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318969</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>A review of nutritional effects on fat composition of animal products with special emphasis on n-3 Polyunsaturated fatty acids.</title>
            <link>http://www.medworm.com/index.php?rid=3318968&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188790%26dopt%3DAbstract</link>
            <description>Authors: Kouba M, Mourot J
    The fatty acid composition of animal products (eggs, milk and meat) is the reflect of both the tissue fatty acid biosynthesis and the fatty acid composition of ingested lipids. This relationship is stronger in monogastrics (pigs, poultry and rabbits) than in ruminants, where dietary fatty acids are hydrogenated in the rumen. There is an increasing recognition of the health benefits of polyunsaturated fatty acids (PUFA), because these fatty acids are essential for humans. In addition, the ratio n-6/n-3 fatty acids in the human diet is important. This ratio by far exceeds the recommended value of 5. Therefore, inclusion of fish meals, or n-3 PUFA rich oils, or linseed in animal diets is a valid means of meeting consumer demand for animal products that are nutri...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318968</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Structural Determinants of Host Defense Peptides for Antimicrobial Activity and Target Cell Selectivity.</title>
            <link>http://www.medworm.com/index.php?rid=3318967&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188791%26dopt%3DAbstract</link>
            <description>Authors: Takahashi D, Shukla SK, Prakash O, Zhang G
    Antimicrobial host defense peptides (HDPs) are a critical component of the innate immunity with microbicidal, endotoxin-neutralizing, and immunostimulatory properties. HDPs kill bacteria primarily through non-specific membrane lysis, therefore with a less likelihood of provoking resistance. Extensive structure-activity relationship studies with a number of HDPs have revealed that net charge, amphipathicity, hydrophobicity, and structural propensity are among the most important physicochemical and structural parameters that dictate their ability to interact with and disrupt membranes. A delicate balance among these factors, rather than a mere alteration of a single factor, is critically important for HDPs to ensure the antimicrobial po...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318967</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Molecular mechanisms involved in the adaptation to amino acid limitation in mammals.</title>
            <link>http://www.medworm.com/index.php?rid=3318974&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20188139%26dopt%3DAbstract</link>
            <description>Authors: Fafournoux P, Chaveroux C, Lambert-Langlais S, Cherasse Y, Averous J, Parry L, Carraro V, Jousse C, Maurin AC, Bruhat A
    In mammals, metabolic adaptations are required to cope with episodes of protein deprivation and malnutrition. Consequently, mammals have to adjust physiological functions involved in the adaptation to amino acid availability. Part of this regulation involves the modulation of the expression of numerous genes. In particular, it has been shown that amino acids by themselves can modify the expression of target genes. This review describes the regulation of amino acids homeostasis and the their role as signal molecules. The recent advances in the understanding of the molecular mechanisms involved in the control of mammalian gene expression in response to amino ac...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3318974</comments>
            <pubDate>Tue, 23 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3318974</guid>        </item>
        <item>
            <title>Structural modifications of nucleosides in ionic liquids.</title>
            <link>http://www.medworm.com/index.php?rid=3311672&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178825%26dopt%3DAbstract</link>
            <description>This article summarizes recent efforts on nucleoside modification using ionic liquids.
    PMID: 20178825 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311672</comments>
            <pubDate>Sat, 20 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311672</guid>        </item>
        <item>
            <title>Drastic changes in fecal and mucosa-associated microbiota in adult patients with short bowel syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=3302907&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20172013%26dopt%3DAbstract</link>
            <description>Authors: Joly F, Mayeur C, Bruneau A, Noordine ML, Meylheuc T, Langella P, Messing B, Du&amp;#xE9;e PH, Cherbuy C, Thomas M
    Short bowel syndrome (SBS) is observed in Humans after a large resection of gut. Since the remnant colon and its associated-microbiota play a major role in the outcome of patients with SBS, we studied the overall qualitative and quantitative microbiota composition of SBS adult patients compared to controls. The population was composed of 11 SBS type II patients (with a jejuno-colonic anastomosis) and 8 controls without intestinal pathology. SBS patients had 38+/-30cm remnant small bowel length and 66+/-19% of residual colon. The repartition of proteins, lipids, carbohydrates and fibres was expressed as % of total oral intake in patients and controls. The microbiota wa...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3302907</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3302907</guid>        </item>
        <item>
            <title>Enhancement of the adhesive and spreading potentials of ovarian carcinoma RMG-1 cells due to increased expression of integrin alpha5beta1 with the Lewis Y-structure on transfection of the alpha1,2-fucosyltransferase gene.</title>
            <link>http://www.medworm.com/index.php?rid=3302906&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20172014%26dopt%3DAbstract</link>
            <description>Authors: Yan LM, Lin B, Zhu LC, Hao YY, Qi Y, Wang CZ, Gao S, Liu SC, Zhang SL, Iwamori M
    Le(Y) antigen is known to be associated with malignant properties including metastasis and a poor prognosis of ovarian carcinomas. To clarify the mechanisms underling these properties, we established ovarian carcinoma-derived cells exhibiting enhanced expression of Le(Y) by transfection with alpha1,2-fucosyltransferase and compared their cellular properties with those of the original cells. So the human alpha1,2-fucosyltransferase gene was transfected into ovarian carcinoma-derived RMG-1 cells, which are known to contain Le(X), a precursor of Le(Y), and RMG-1-hFUT cells exhibiting enhanced expression of Le(Y) were established by selection with anti-Le(Y) antibodies, and their adhesive and spreadin...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3302906</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3302906</guid>        </item>
        <item>
            <title>Comparative reactivity of mismatched and unpaired bases in relation to their type and surroundings. Chemical Cleavage of DNA Mismatches in Mutation detection analysis.</title>
            <link>http://www.medworm.com/index.php?rid=3302909&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20171258%26dopt%3DAbstract</link>
            <description>This study provides a complete understanding of the principles of mutation detection methodology based on chemical cleavage of mismatches and clarifies the advantages and limitations of this approach in various biological and conformational studies of DNA.
    PMID: 20171258 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3302909</comments>
            <pubDate>Wed, 17 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3302909</guid>        </item>
        <item>
            <title>Carbohydrate binding specificities and crystal structure of the cholera toxin-like B-subunit from Citrobacter freundii.</title>
            <link>http://www.medworm.com/index.php?rid=3302908&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20171259%26dopt%3DAbstract</link>
            <description>Authors: Jansson L, Angstr&amp;#xF6;m J, Lebens M, Imberty A, Varrot A, Teneberg S
    Enterotoxigenic Escherichia coli and Vibrio cholerae are well known causative agents of severe diarrheal diseases. Both pathogens produce AB(5) toxins, with one enzymatically active A-subunit and a pentamer of receptor-binding B-subunits. The primary receptor for both B-subunits is the GM1 ganglioside (Galbeta3GalNAcbeta4(NeuAcalpha3)Galbeta4GlcbetaCer), but the B-subunits from porcine isolates of E. coli also bind neolacto-(Galbeta4GlcNAcbeta-)terminated glycoconjugates and the B-subunits from human isolates of E. coli (hLTB) have affinity for blood group A type 2-(GalNAcalpha3(Fucalpha2)Galbeta4GlcNAcbeta-)terminated glycoconjugates. A B-subunit with 73% sequence identity to the B-subunits of cholera toxin...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3302908</comments>
            <pubDate>Wed, 17 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3302908</guid>        </item>
        <item>
            <title>The Platelet Activating Factor (PAF) Signaling Cascade in Systemic Inflammatory Responses.</title>
            <link>http://www.medworm.com/index.php?rid=3291301&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20167241%26dopt%3DAbstract</link>
            <description>Authors: Yost CC, Weyrich AS, Zimmerman GA
    The platelet activating factor (PAF) signaling cascade evolved as a component of the repertoire of innate host defenses, but is also an effector pathway in inflammatory and thrombotic diseases. This review focuses on the PAF signaling cascade in systemic inflammatory responses and, specifically, explores its activities in experimental and clinical sepsis and anaphylaxis in the context of the basic biochemistry and biology of signaling via this lipid mediator system.
    PMID: 20167241 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291301</comments>
            <pubDate>Mon, 15 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3291301</guid>        </item>
        <item>
            <title>Efficient Use and Recycling of the Micronutrient Iodide in Mammals.</title>
            <link>http://www.medworm.com/index.php?rid=3291300&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20167242%26dopt%3DAbstract</link>
            <description>Authors: Rokita SE, Adler JM, McTamney PM, Watson JA
    Daily ingestion of iodide alone is not adequate to sustain production of the thyroid hormones, tri- and tetraiodothyronine. Proper maintenance of iodide in vivo also requires its active transport into the thyroid and its salvage from mono- and diiodotyrosine that are formed in excess during hormone biosynthesis. The enzyme iodotyrosine deiodinase responsible for this salvage is unusual in its ability to catalyze a reductive dehalogenation reaction dependent on a flavin cofactor, FMN. Initial characterization of this enzyme was limited by its membrane association, difficult purification and poor stability. The deiodinase became amenable to detailed analysis only after identification and heterologous expression of its gene. Site-direct...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291300</comments>
            <pubDate>Mon, 15 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3291300</guid>        </item>
        <item>
            <title>Calorimetric and Spectroscopic Studies of Aminoglycoside Binding to AT-rich DNA Triple Helices.</title>
            <link>http://www.medworm.com/index.php?rid=3291299&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20167243%26dopt%3DAbstract</link>
            <description>Authors: Xi H, Kumar S, Dosen-Micovic L, Arya DP
    Calorimetric and fluorescence techniques were used to characterize the binding of aminoglycosides-neomycin, paromomycin, and ribostamycin, with 5'-dA(12)-x-dT(12)-x-dT(12)-3' intramolecular DNA triplex (x = hexaethylene glycol) and poly(dA)*2poly(dT) triplex. Our results demonstrate the following features: (1) UV thermal analysis reveals that the T(m) for triplex decreases with increasing pH value in the presence of neomycin, while the T(m) for the duplex remains unchanged. (2) The binding affinity of neomycin decreases with increased pH, although there is an increase in observed binding enthalpy. (3) ITC studies conducted in two buffers (sodium cacodylate and MOPS) yield the number of protonated drug amino groups (Deltan) as 0.29 and 0....</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291299</comments>
            <pubDate>Mon, 15 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3291299</guid>        </item>
        <item>
            <title>S1P metabolism in cancer and other pathological conditions.</title>
            <link>http://www.medworm.com/index.php?rid=3291298&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20167244%26dopt%3DAbstract</link>
            <description>Authors: Leong WI, Saba JD
    Nearly two decades ago, the sphingolipid metabolite sphingosine 1-phosphate was discovered to function as a lipid mediator and regulator of cell proliferation. Since that time, sphingosine 1-phosphate has been shown to mediate a diverse array of fundamental biological processes including cell proliferation, migration, invasion, angiogenesis, vascular maturation and lymphocyte trafficking. Sphingosine 1-phosphate acts primarily via signaling through five ubiquitously expressed G protein-coupled receptors. Intracellular sphingosine 1-phosphate molecules are transported extracellularly and gain access to its cognate receptors for autocrine and paracrine fashion and for signaling at distant sites reached through blood and lymphatic circulation systems. Intracellu...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291298</comments>
            <pubDate>Mon, 15 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3291298</guid>        </item>
        <item>
            <title>Beneficial effects of omega-3 long-chain fatty acids in breast cancer and cardiovascular diseases: Voltage-gated sodium channels as a common feature?</title>
            <link>http://www.medworm.com/index.php?rid=3291297&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20167245%26dopt%3DAbstract</link>
            <description>Authors: Gillet L, Roger S, Bougnoux P, Le Guennec JY, Besson P
    Cancers are among the leading causes of death worldwide. Voltage-gated sodium channels, among other ion channels, appear as new molecular players in epithelial cancers. Highly metastatic breast cancer cells express Na(V)1.5, the main isoform expressed in cardiac cells, where the current generated by the flux of sodium ions is responsible for the excitability. Breast cancer cells are not excitable and the protein activity regulates cell invasiveness, through the modulation of activity of acidic cathepsins, a characteristic involved in the metastatic phenotype. Interestingly, it is known that omega-3 LC-PUFA can exert beneficial effects by preventing post-myocardial infarction arrhythmias and by reducing the incidence of met...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291297</comments>
            <pubDate>Mon, 15 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3291297</guid>        </item>
        <item>
            <title>Prostaglandin E synthases: Understanding their pathophysiological roles through mouse genetic models.</title>
            <link>http://www.medworm.com/index.php?rid=3284580&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20159030%26dopt%3DAbstract</link>
            <description>Authors: Hara S, Kamei D, Sasaki Y, Tanemoto A, Nakatani Y, Murakami M
    Prostaglandin E synthase (PGES), which converts cyclooxygenase (COX)-derived prostaglandin H(2) (PGH(2)) to PGE(2), is known to comprise a group of at least three structurally and biologically distinct enzymes. Two of them are membrane-bound and have been designated as mPGES-1 and mPGES-2. mPGES-1 is a perinuclear protein that is markedly induced by proinflammatory stimuli and down-regulated by anti-inflammatory glucocorticoids as in the case of COX-2.It is functionally coupled with COX-2 in marked preference to COX-1. mPGES-2 is synthesized as a Golgi membrane-associated protein, and the proteolytic removal of the N-terminal hydrophobic domain leads to the formation of a mature cytosolic enzyme. This enzyme is rath...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3284580</comments>
            <pubDate>Sat, 13 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3284580</guid>        </item>
        <item>
            <title>mPGES-1 as a Target for Cancer Suppression.</title>
            <link>http://www.medworm.com/index.php?rid=3284579&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20159031%26dopt%3DAbstract</link>
            <description>Authors: Nakanishi M, Gokhale V, Meuillet EJ, Rosenberg DW
    Prostaglandin E(2) (PGE(2)) is a bioactive lipid that can elicit a wide range of biological effects associated with inflammation and cancer. The physiological roles of PGE(2) are diverse, mediated in part through activation of key downstream signaling cascades via transmembrane EP receptors located on the cell surface. Elevated levels of COX-2 and concomitant overproduction of PGE(2) are often found in human cancers. These observations have led to the use of non-steroidal anti-inflammatory drugs (NSAIDs) as chemopreventive agents, particularly for colorectal cancer (CRC). Their long-term use, however, may be associated with gastrointestinal toxicity and increased risk of adverse cardiovascular events, prompting the development ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3284579</comments>
            <pubDate>Sat, 13 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3284579</guid>        </item>
        <item>
            <title>STAT1 and pathogens, not a friendly relationship.</title>
            <link>http://www.medworm.com/index.php?rid=3284578&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20159032%26dopt%3DAbstract</link>
            <description>Authors: Najjar I, Fagard R
    STAT1 belongs to the STAT family of transcription factors, which comprises seven factors: STAT1, STAT2, STAT3, STAT4, STAT5A, STAT5B and STAT6. STAT1 is a 91kDa protein originally identified as the mediator of the cellular response to interferon (IFN)alpha, and thereafter found to be a major component of the cellular response to IFNgamma. STAT1 is, in fact, involved in the response to several cytokines and to growth factors. It is activated by cytokine receptors via kinases of the JAK family. STAT1 becomes phosphorylated and forms a dimer which enters the nucleus and triggers the transcription of its targets. Although not lethal at birth, selective gene deletion of STAT1 in mice leads to rapid death from severe infections, demonstrating its major role in the...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3284578</comments>
            <pubDate>Sat, 13 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3284578</guid>        </item>
        <item>
            <title>Sphingosine Kinase: Role in Regulation of Bioactive Sphingolipid Mediators in Inflammation.</title>
            <link>http://www.medworm.com/index.php?rid=3284581&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20156522%26dopt%3DAbstract</link>
            <description>Authors: Snider AJ, Orrgandy KA, Obeid LM
    Sphingolipids and their synthetic enzymes are emerging as important mediators in inflammatory responses and as regulators of immune cell functions. In particular, sphingosine kinase (SK) and its product sphingosine-1-phosphate (S1P) have been extensively implicated in these processes. SK catalyzes the phosphorylation of sphingosine to S1P and exists as two isoforms, SK1 and SK2. SK1 has been shown to be activated by cytokines including tumor necrosis factor-alpha (TNF-alpha) and interleukin1-beta (IL1-beta). The activation of SK1 in this pathway has been shown to be, at least in part, required for mediating TNF-alpha and IL1-beta inflammatory responses in cells, including induction of cyclo-oxygenase 2 (COX-2). In addition to their role in infl...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3284581</comments>
            <pubDate>Fri, 12 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3284581</guid>        </item>
        <item>
            <title>Extracellular phospholipases in atherosclerosis.</title>
            <link>http://www.medworm.com/index.php?rid=3276667&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20153800%26dopt%3DAbstract</link>
            <description>Authors: Karabina SA, Gora S, Atout R, Ninio E
    Phospholipases A2 (PLA2) are a family of enzymes that catalyze the hydrolysis of the sn-2 ester bond of glycerophospholipids liberating lysophospholipids and free fatty acids; important second messengers involved in atherogenesis. Plasma PAF-acetylhydrolase (PAF-AH) or Lp-PLA2 is a Ca(2+)-independent PLA2 which is produced by monocyte-derived macrophages and by activated platelets, and circulates in plasma associated with lipoproteins. PAF-AH catalyzes the removal of the acetyl/short acyl group at the sn-2 position of PAF and oxidized phospholipids produced during inflammation and oxidative stress. In humans, PAF-AH is mainly associated with small dense LDL and to a lesser extent with HDL and with lipoprotein(a). PAF-AH is N-glycosylated p...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3276667</comments>
            <pubDate>Thu, 11 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3276667</guid>        </item>
        <item>
            <title>Novel families of antimicrobial peptides with multiple functions from skin of Xizang plateau frog, Nanorana parkeri.</title>
            <link>http://www.medworm.com/index.php?rid=3276666&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20153801%26dopt%3DAbstract</link>
            <description>Authors: Lu Z, Zhai L, Wang H, Che Q, Wang D, Feng F, Zhao Z, Yu H
    Xizang plateau frog (Nanorana parkeri) captured in Lhasa, Tibet, China, solely lives in the subtropical plateau, where there is strong ultraviolet radiation and long duration of sunshine. Considering its harsh living environment, the frog's innate defense against microbes and environmental stress was investigated. In current study, three antimicrobial peptides (AMPs) were purified and characterized from the skin secretion of N. parkeri. The coding cDNA sequences were also cloned from the skin cDNA library of N. parkeri. By structural characterization, two peptides were identified belonging to Japonnicin-1 family, and named as Japonnicin-1Npa (FLLFPLMCKIQGKC) and Japonnicin-1Npb (FVLPLVMCKILRKC). The third peptide isolat...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3276666</comments>
            <pubDate>Thu, 11 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3276666</guid>        </item>
        <item>
            <title>Heteromeric connexin 43/connexin 33 complex endocytosis: a connexin phosphorylation independent mechanism.</title>
            <link>http://www.medworm.com/index.php?rid=3276668&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20152878%26dopt%3DAbstract</link>
            <description>Authors: Diane C, J&amp;#xE9;rome G, Dominique S, Georges P
    The role of gap junctions in proliferation, differentiation and apoptosis has been recently highlighted. Nevertheless, the molecular mechanisms that control these physiological events by acting on gap junction channels are still unknown. We have recently demonstrated that heteromeric gap junction plaques composed by Cx43 and Cx33 are unstable at the cell boundary and are rapidly internalized by endocytosis. In the present study, we analyze the phosphorylation status of Cx43 in homomeric (Cx43/Cx43) and heteromeric (Cx33/Cx43) complexes and their association with the tyrosine kinase c-Src. Our data show that c-Src interaction and P2 phosphorylation of Cx43, which are essential for homomeric Cx43 complex endocytosis, were altered in...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3276668</comments>
            <pubDate>Tue, 09 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3276668</guid>        </item>
        <item>
            <title>Thiol-Disulfide Exchanges Modulate Aldo-Keto Reductase Family 1 Member B10 Activity And Sensitivity To Inhibitors.</title>
            <link>http://www.medworm.com/index.php?rid=3263001&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20144905%26dopt%3DAbstract</link>
            <description>In this study, we found that aldo-keto reductase family 1 member B10 (AKR1B10) contains 4 Cys residues, i.e., Cys45, Cys187, Cys200, and Cys299. Exposing AKR1B10 to ROS mixtures resulted in significant decrease of its free sulfhydryl groups, up to 40-50% in the presence of physiological thiol cysteine at 0.5 or 1.0 mM; and accordingly, AKR1B10 enzymatic activity was reversibly decreased, in parallel with the oxidation of the sulfhydryl groups. ROS-induced thiolation also affected the sensitivity of AKR1B10 to inhibitors EBPC, epalrestat, and statil. Together our results showed for the first time that AKR1B10's enzymatic activity and inhibitor sensitivity are modulated by thiol/disulfide exchanges.
    PMID: 20144905 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263001</comments>
            <pubDate>Sat, 06 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3263001</guid>        </item>
        <item>
            <title>Type-IIa secreted phospholipase A(2) is an endogenous antibiotic-like protein of the host.</title>
            <link>http://www.medworm.com/index.php?rid=3263005&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20144678%26dopt%3DAbstract</link>
            <description>Authors: Wu Y, Raymond B, Goosens P, Njamkepo E, Guiso N, Paya M, Touqui L
    Type-IIA secreted phospholipase A(2) (sPLA(2)-IIA) has been proposed to play a role in the development of inflammatory diseases. It has been shown to release arachidonic acid, the precursor of proinflammatory eicosanoids, to hydrolyze phospholipids of pulmonary surfactant, and to bind to specific receptors located on cell surface membranes. However, the most established biological role of sPLA(2)-IIA is related to its potent bactericidal property in particular toward Gram-positive bacteria. This enzyme is present in animal and human biological fluids at concentrations sufficient to kill bacteria. Human recombinant sPLA(2)-IIA is able to kill Gram-positive bacteria at concentrations as low as 1.1 ng/ml. This rema...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263005</comments>
            <pubDate>Fri, 05 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3263005</guid>        </item>
        <item>
            <title>Filamentous actin and its associated binding proteins are the stimulatory site for 6-phosphofructo-1-kinase association within the membrane of human erythrocytes.</title>
            <link>http://www.medworm.com/index.php?rid=3263004&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20144679%26dopt%3DAbstract</link>
            <description>Authors: Real-Hohn A, Zancan P, Da Silva D, Martins ER, Salgado LT, Mermelstein CS, Gomes AM, Sola-Penna M
    Glycolytic enzymes reversibly associate with the human erythrocyte membrane (EM) as part of their regulatory mechanism. The site for this association has been described as the amino terminus of band 3, a transmembrane anion transporter. Binding of glycolytic enzymes to this site is recognized to inhibit glycolysis, since binding inhibits the catalytic activity of these enzymes, including the rate-limiting enzyme 6-phosphofructo-1-kinase (PFK). However, the existence of a putative stimulatory site for glycolytic enzymes within the EM has been proposed. PFK has been described as able to reversibly associate with other proteins, such as microtubules, which inhibit the enzyme, and fil...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263004</comments>
            <pubDate>Fri, 05 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3263004</guid>        </item>
        <item>
            <title>LysK, the enzyme lysing Staphylococcus aureus cells: Specific kinetic features and approaches towards stabilization.</title>
            <link>http://www.medworm.com/index.php?rid=3263003&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20144680%26dopt%3DAbstract</link>
            <description>Authors: Filatova LY, Becker SC, Donovan DM, Gladilin AK, Klyachko NL
    LysK, the enzyme lysing cells of Staphylococcus aureus, can be considered as perspective antimicrobial agent. Knowledge of LysK properties and behavior would allow optimizing conditions of its storage as well as formulating strategy towards its stabilization. Reaction of LysK with substrate (suspension of autoclaved Staphylococcus aureus cells) has been found to be adequately described by the two-stage Michaelis-Menten kinetic scheme. Ionization of the enzyme and enzyme-substrate complex important for revealing catalytic activity is controlled by two ionogenic groups with pK 6.0 and 9.6. Ionization energy of the group with pK 6.0 is of 30 kJ/mol, thus, pointing out on His residue; pK 9.6 might be attributed to metal ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263003</comments>
            <pubDate>Fri, 05 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3263003</guid>        </item>
        <item>
            <title>Serum Response Factor depletion affects the proliferation of the hepatocellular carcinoma cells HepG2 and JHH6.</title>
            <link>http://www.medworm.com/index.php?rid=3263002&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20144681%26dopt%3DAbstract</link>
            <description>In conclusion, SRF depletion affects the expansion of the high and low differentiation grade HCC cells HepG2 and JHH6. These results can pave the way to understand the role of SRF in HCC development and possibly to identify novel anti HCC therapeutic strategies.
    PMID: 20144681 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263002</comments>
            <pubDate>Fri, 05 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3263002</guid>        </item>
        <item>
            <title>DNA-hydrolyzing activity of IgG antibodies from the sera of patients with tick-borne encephalitis.</title>
            <link>http://www.medworm.com/index.php?rid=3255023&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138955%26dopt%3DAbstract</link>
            <description>Authors: Parkhomenko TA, Buneva VN, Tyshkevich OB, Generalov II, Doronin BM, Nevinsky GA
    DNase autoantibodies (Abzs) can be found in the blood of patients with several autoimmune diseases, while the blood of healthy donors or patients with diseases with an insignificant disturbance of the immune status does not contain DNase Abzs. Here we present the first analysis of the DNase Abzs activity in the patients with tick-borne encephalitis (TBE). Several strict criteria have been applied to show that the DNase activity is an intrinsic property of IgGs from the sera of TBE patients but not from healthy donors. The relative activity of IgGs has been shown to vary extensively from patient to patient, but most of the preparations (91%) had detectable levels of the DNase activity. Polyclonal DN...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255023</comments>
            <pubDate>Thu, 04 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255023</guid>        </item>
        <item>
            <title>Biochemical and structural properties of gamma-glutamyl transpeptidase from Geobacillus thermodenitrificans: An enzyme specialized in hydrolase activity.</title>
            <link>http://www.medworm.com/index.php?rid=3255024&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138205%26dopt%3DAbstract</link>
            <description>Authors: Castellano I, Merlino A, Rossi M, La Cara F
    Gamma-glutamyltranspeptidases (gamma-GTs) catalyze the transfer of the gamma-glutamyl moiety of glutathione and related gamma-glutamyl amides to water (hydrolysis) or to amino acids and peptides (transpeptidation) and play a key role in glutathione metabolism. Recently, gamma-GTs have been considered attractive pharmaceutical targets for cancer and useful tools to produce gamma-glutamyl compounds. To find out gamma-GTs with special properties we have chosen microorganisms belonging to Geobacillus species which are source of several thermostable enzymes of potential interest for biotechnology. gamma-GT from Geobacillus thermodenitrificans (GthGT) was cloned, expressed in Escherichia coli, purified to homogeneity and characterized. The...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255024</comments>
            <pubDate>Wed, 03 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255024</guid>        </item>
        <item>
            <title>Equilibrium and Kinetics of the Unfolding and Refolding of Escherichia coli Malate Synthase G monitored by circular dichroism and fluorescence spectroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=3255028&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138106%26dopt%3DAbstract</link>
            <description>Authors: Maheshwari A, Verma VK, Chaudhuri TK
    The equilibrium and kinetics studies of an 82kDa large monomeric E.coli protein Malate synthase G (MSG) was investigated by far and near-UV CD, intrinsic tryptophan fluorescence and extrinsic fluorescence spectroscopy. We find that despite of its large size, folding is reversible, in-vitro. Equilibrium unfolding process of MSG exhibited three-state transition thus, indicating the presence of atleast a stable equilibrium intermediate. Thermodynamic parameters suggest this intermediate resembles the unfolded state. However, the equilibrium intermediate exhibits pronounced secondary structure as measured by far-UV CD, partial tertiary structure as delineated by near-UV CD, compactness (m value) and exposed hydrophobic surface area as assessed ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255028</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255028</guid>        </item>
        <item>
            <title>Compacting effect of BBR3464, a new-generation trisplatinum anticancer agent, on DNA.</title>
            <link>http://www.medworm.com/index.php?rid=3255027&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138107%26dopt%3DAbstract</link>
            <description>Authors: Banerjee T, Dubey P, Mukhopadhyay R
    BBR3464 is a trinuclear platinum compound of formula [{trans-PtCl(NH(3))(2)}(2)-mu-trans-Pt(NH(3))(2){NH(2)(CH(2))(6)NH(2)}(2)] (4+). It is a new-generation platinum chemotherapeutic agent that exhibits cytotoxicity at ten to thousand times lower dose limit compared to the well-known platinum drug cisplatin, in cisplatin-sensitive as well as in cisplatin-resistant cells. DNA is thought to be the primary cellular target of BBR3464. In this work, we have applied high-resolution atomic force microscopy (AFM) for the first time, to obtain direct information on BBR3464-induced structural changes of DNA. It is found that the DNA molecules get compacted after treatment with BBR3464, for the drug:DNA molar ratio and the drug treatment period of 0.01...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255027</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255027</guid>        </item>
        <item>
            <title>1-Cysteine Peroxiredoxin: A Dual Function Enzyme with Peroxidase and Acidic Ca(2+)-independent Phospholipase A(2) Activities. Review.</title>
            <link>http://www.medworm.com/index.php?rid=3255026&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138108%26dopt%3DAbstract</link>
            <description>Authors: Nevalainen TJ
    Peroxiredoxins (Prx) are enzymes that catalyze the reduction of hydrogen peroxide and alkyl hydroperoxides. Prxs are ubiquitous enzymes with representatives found in Bacteria, Archaea and Eukarya. Many 1-cysteine peroxiredoxins (1-CysPrx) are dual function enzyme with both peroxidase and acidic Ca(2+)-independent phospholipase A(2) (aiPLA(2)) activities. The functions proposed for 1-CysPrx/aiPLA(2) include the protection of cell membrane phospholipids against oxidative damage (peroxidation) and the metabolism (hydrolysis) of phospholipids, such as those of lung surfactant. The peroxidase active site motif PVCTTE of 1-CysPrx contains the conserved catalytic cysteine residue, and the esterase (lipase) motif GXSXG of the enzyme contains the conserved catalytic serin...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255026</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255026</guid>        </item>
        <item>
            <title>Structural Requirement for PPARgamma Binding Revealed by a Meta Analysis of holo-Crystal Structures.</title>
            <link>http://www.medworm.com/index.php?rid=3255025&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138109%26dopt%3DAbstract</link>
            <description>Authors: Nascimento AS
    PPARgamma is a ligand regulated transcriptional factor that modulates the transcription of several genes involved in fat and sugar metabolism. Due to its easy bacterial expression and crystallization, several crystal structures of holo-PPARgamma have been reported and deposited in the Protein Data Bank. Here, we investigated the three dimensional electrostatic properties of 55 PPARgamma ligands and used this information for clustering them through principal component analysis. We found out that, according to their electrostatic potential, these ligands can be separated in three groups, with different binding features. We also observed that non-selective and selective ligands show different 3D electrostatic properties and are separated in different clusters. The r...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255025</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255025</guid>        </item>
        <item>
            <title>Nucleic acid and protein factors involved in Escherichia coli polynucleotide phosphorylase function on RNA.</title>
            <link>http://www.medworm.com/index.php?rid=3236640&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20114069%26dopt%3DAbstract</link>
            <description>Authors: Fern&amp;#xE1;ndez-Ram&amp;#xED;rez F, Berm&amp;#xFA;dez-Cruz RM, Monta&amp;#xF1;ez C
    It has been reported that polynucleotide phosphorylase (PNPase) binds to RNA via KH and S1 domains, and at least two main complexes (I &amp; II) have been observed in RNA binding assays. Here we describe PNPase binding to RNA, the factors involved in this activity and the nature of the interactions observed in vitro. Our results show that RNA length and composition affect PNPase binding, and that PNPase interacts primarily with the 3'-end of RNA, forming the complex I-RNA, which contains trimeric units of PNPase. When the 5'-end of RNA is blocked by a hybridizing oligonucleotide, the formation of complex II-RNA is inhibited. In addition, PNPase was found to form high molecular weight (&amp;gt;440 kDa) aggregates...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3236640</comments>
            <pubDate>Tue, 26 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3236640</guid>        </item>
        <item>
            <title>Synthesis and Evaluation of Conformationally Constrained Peptide Analogues as the Src SH3 Domain Binding Ligands.</title>
            <link>http://www.medworm.com/index.php?rid=3223893&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20109515%26dopt%3DAbstract</link>
            <description>Authors: Tiwari R, Brown A, Narramaneni S, Sun G, Parang K
    Src kinase activity is regulated by the interaction of SH3 domain with protein sequences that are rich in proline residues. Identification of more potent SH3 domain binding ligands that can regulate Src kinase activity is a subject of major interest. Conformationally constrained peptides have been previously used for improving the binding potency of the Src SH2 domain binding peptide ligands and peptide substrates of the substrate-binding site of Src. A series of peptide analogues of Ac-VSLARRPLPPLP (1, Ac-VSL-12, K(d) = 0.34 muM) were synthesized by introducing conformational constraints to improve the binding affinity towards the Src SH3 domain. Peptides synthesized through cyclization between N-terminal to C-terminal [VSLARR...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3223893</comments>
            <pubDate>Mon, 25 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3223893</guid>        </item>
        <item>
            <title>Calreticulin Transacylase: Genesis, mechanism of action and biological applications.</title>
            <link>http://www.medworm.com/index.php?rid=3223892&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20109516%26dopt%3DAbstract</link>
            <description>Authors: Kumari R, Bansal S, Gupta G, Arora S, Kumar A, Goel S, Singh P, Ponnan P, Priya N, Tyagi TK, Baghel AS, Manral S, Tandon R, Joshi R, Rohil V, Gaspari M, Kohli E, Tyagi YK, Dwarakanath BS, Saluja D, Chatterji S, Sharma SK, Prasad AK, Rastogi RC, Raj HG, Parmar VS
    Our earlier investigations have identified a unique enzyme in the endoplasmic reticulum (ER) termed Acetoxy Drug: Protein Transacetylase (TAase) catalyzing the transfer of acetyl group from polyphenolic acetates (PA) to certain receptor proteins (RP). An elegant assay procedure for TAase was developed based on the inhibition of glutathione S-transfesrase (GST) due to acetylation by a model acetoxycoumarin, 7, 8-Diacetoxy-4-methylcoumarin (DAMC). TAase purified from various mammalian tissue microsomes to homogeneity exh...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3223892</comments>
            <pubDate>Mon, 25 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3223892</guid>        </item>
        <item>
            <title>Biochemical, functional and structural characterization of Akbu-LAAO: A novel snake venom L-amino acid oxidase from Agkistrodon blomhoffii ussurensis.</title>
            <link>http://www.medworm.com/index.php?rid=3212772&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20100538%26dopt%3DAbstract</link>
            <description>Authors: Sun MZ, Guo C, Tian Y, Chen D, Greenaway FT, Liu S
    An L-amino acid oxidase (Akbu-LAAO) was isolated from the venom of Agkistrodon blomhoffii ussurensis snake using DEAE Sephadex A-50 ion-exchange, Sephadex G-75 gel filtration, and high performance liquid chromatographies. The homogeneity and molecular mass of Akbu-LAAO were analyzed by SDS-PAGE and MALDI-TOF spectrometry. The sequences of ten peptides from Akbu-LAAO were established by HPLC-nESI-MS/MS analysis. Protein sequence alignment indicated that i) that Akbu-LAAO is a new snake venom LAAO, and ii) Akbu-LAAO shares homology with several LAAOs from the venoms of Calloselasma rhodost, Agkistrodon halys, Daboia russellii siamensis, and Trimeresurus stejnegeri. Akbu-LAAO is a homodimer with a molecular mass of ~124.4kDa. It ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212772</comments>
            <pubDate>Fri, 22 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212772</guid>        </item>
        <item>
            <title>Iron transport by proteoliposomes containing mitochondrial F(1)F(o) ATP synthase isolated from rat heart.</title>
            <link>http://www.medworm.com/index.php?rid=3212771&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20100539%26dopt%3DAbstract</link>
            <description>Authors: Kim M, Song E
    In this work, we present evidence of Fe(2+) transport by rat heart mitochondrial F(1)F(o) ATP synthase. Iron uptake by the vesicles containing the enzyme was concentration- and temperature-dependent, with an optimum temperature of 37 degrees C. Both ATP and ADP stimulated iron uptake in a concentration-dependent manner, whereas AMP, AMPPCP, and mADP did not. Inhibitors of the enzyme, oligomycin, and resveratrol similarly blocked iron transport. The iron uptake was confirmed by inhibition using specific antibodies against the alpha, beta, and c subunits of the enzyme. Interestingly, slight transport of common divalent and trivalent metal ions such as Mg(+2), Ca(+2), Mn(+2), Zn(+2), Cu(+2), Fe(+3), and Al(+3) was observed. Moreover, Cu(+2), even in the nM range, in...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212771</comments>
            <pubDate>Fri, 22 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212771</guid>        </item>
        <item>
            <title>Regulation of CIRL-1 proteolysis and trafficking.</title>
            <link>http://www.medworm.com/index.php?rid=3212770&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20100540%26dopt%3DAbstract</link>
            <description>In this study, we demonstrate that activators of protein kinase C-PMA and ionomycin, can inhibit the cleavage of CIRL-1 precursor in transfected cells. Both reagents also downregulate trafficking of CIRL-1 to the cell surface that results in accumulation of the uncleaved receptor precursor inside the cells. Experiments with a non-cleavable soluble mutant of CIRL-1 showed that the downregulation of the receptor trafficking is independent of its cleavage. Our data suggest that the GPS proteolysis of CIRL-1 is not a purely autocatalytic process and may involve auxiliary proteins or factors that become available in the course of CIRL-1 trafficking.
    PMID: 20100540 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212770</comments>
            <pubDate>Fri, 22 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212770</guid>        </item>
        <item>
            <title>Characterization of Two Linear Cationic Antimalarial Peptides in the Scorpion Mesobuthus eupeus.</title>
            <link>http://www.medworm.com/index.php?rid=3212774&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20097251%26dopt%3DAbstract</link>
            <description>Authors: Gao B, Xu J, Del Carmen Rodriguez M, Lanz-Mendoza H, Hern&amp;#xE1;ndez-Rivas R, Du W, Zhu S
    Plasmodium falciparum is a pathogen of human malaria which causes millions of deaths per year due to the ever-increasing drug resistance by the parasite, and thus novel antimalarial agents are urgently needed. In this work, we report two cDNA clones from the scorpion Mesobuthus eupeus venom gland, which encode peptides inhibiting the development of P. berghei, killing intraerythrocytic P. falciparum, and toxic to the Drosophila S2 cell at micromolar concentrations. One peptide of 24 amino acids (named meucin-24) shares high sequence identity to the amino-terminus of a family of scorpion venom long-chain K(+) channel toxins (LcKTx) and two frog antimicrobial peptides (magainin1 and 2). Sequ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212774</comments>
            <pubDate>Thu, 21 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212774</guid>        </item>
        <item>
            <title>Structures and mechanisms of enzymes in the leukotriene cascade.</title>
            <link>http://www.medworm.com/index.php?rid=3212773&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20097252%26dopt%3DAbstract</link>
            <description>Authors: Rinaldo-Matthis A, Haeggstr&amp;#xF6;m JZ
    Leukotrienes are a family of proinflammatory lipid mediators of the innate immune response and are important signalling molecules in inflammatory and allergic conditions. The leukotrienes are formed from arachidonic acid, which is released from membranes by cPLA(2), and further converted by 5-lipoxygenase to form the labile epoxide leukotriene (LT) A(4). This intermediate is converted by either of the two enzymes, LTA(4) hydrolase or LTC(4) synthase, to form LTB(4) or LTC(4), respectively. In order for 5-lipoxygenase to work efficiently in cells, five lipoxygenase activating protein needs to be present. LTB(4) is one of the most powerful chemotactic agents whereas LTC(4) induces smooth muscle contractions, for example in the airways causin...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212773</comments>
            <pubDate>Thu, 21 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212773</guid>        </item>
        <item>
            <title>The Telomere story or the triumph of an open-minded research.</title>
            <link>http://www.medworm.com/index.php?rid=3212775&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096746%26dopt%3DAbstract</link>
            <description>Authors: Gilson E, S&amp;#xE9;gal-Bendirdjian E
    The Nobel Assembly at Karolinska Institutet has decided to award The Nobel Prize in Physiology or Medicine 2009 jointly to Elizabeth H. Blackburn, Carol W. Greider and Jack W. Szostak for the discovery of &quot;how chromosomes are protected by telomeres and the enzyme telomerase&quot;. This discovery had major impacts within the scientific community and led to intense research in this field. All the studies performed are now the bases for future investigations and stimulate the development of potential new therapies.
    PMID: 20096746 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212775</comments>
            <pubDate>Wed, 20 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212775</guid>        </item>
        <item>
            <title>Interaction of [Ru(bpy)(2)(dppz)](2+) with human telomeric DNA: preferential binding to G-quadruplexes over i-motif.</title>
            <link>http://www.medworm.com/index.php?rid=3212779&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096325%26dopt%3DAbstract</link>
            <description>Authors: Shi S, Geng X, Zhao J, Yao T, Wang C, Yang D, Zheng L, Ji L
    Inspired by the enormous importance attributed to the structure and function of human telomeric DNA, we focus our attention on the interaction of [Ru(bpy)(2)(dppz)](2+) with the guanine-rich single-strand oligomer 5'-AGGGTTAGGGTTAGGGTTAGGG-3' (22AG) and the complementary cytosine-rich strand (22CT). In Na(+) buffer, 22AG may adopt an antiparallel basket quadruplex, whereas, it favours a mixed parallel/antiparallel structure in K(+) buffer. 22CT may self-associate at acidic pH into an i-motif. In this paper, the interaction between [Ru(bpy)(2)(dppz)](2+) and each unusual DNA was evaluated. It was interesting that [Ru(bpy)(2)(dppz)](2+) could promote the human telomeric repeat 22AG to fold into intramolecular antiparall...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212779</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212779</guid>        </item>
        <item>
            <title>Enhancement of the thermostability and the catalytic efficiency of Bacillus pumilus CBS protease by site-directed mutagenesis.</title>
            <link>http://www.medworm.com/index.php?rid=3212778&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096326%26dopt%3DAbstract</link>
            <description>Authors: Jaouadi B, Aghajari N, Haser R, Bejar S
    The serine alkaline protease, SAPB, from Bacillus pumilus CBS is characterized by its high thermoactivity, pH-stability and high catalytic efficiency (k(cat)/K(m)) as well as its excellent stability and compatibility with an alkaline environment under harsh washing conditions. Based on sequence alignments and homology-modeling studies, the present study identified five amino acids Leu31, Thr33, Asn99, Phe159 and Gly182 being putatively important for the enzymatic behaviour of SAPB. To corroborate the role of these residues, 12 mutants were constructed by site-directed mutagenesis and then purified and characterized. The findings demonstrate that the single mutants F159T, F159S and G182S and combined double substitutions were implicated i...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212778</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212778</guid>        </item>
        <item>
            <title>N-Palmitoylethanolamine: Biochemistry And New Therapeutic Opportunities.</title>
            <link>http://www.medworm.com/index.php?rid=3212777&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096327%26dopt%3DAbstract</link>
            <description>Authors: Petrosino S, Iuvone T, Di Marzo V, 
    Although its presence in mammalian tissues has been known since the 1960's, N-palmitoyl-ethanolamine (PEA) has emerged only recently among other bioactive N-acylethanolamines as an important local pro-homeostatic mediator which, due to its chemical stability, can be also administered exogenously as the active principle of anti-inflammatory and analgesic preparations (e.g. Normast(R), Pelvilen(R)). Much progress has been made towards the understanding of the mechanisms regulating both the tissue levels of PEA under physiological and pathological conditions, and its pharmacological actions. Here we review these new developments in PEA biochemistry and pharmacology, and discuss novel potential indications for the therapeutic use of this compoun...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212777</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212777</guid>        </item>
        <item>
            <title>Methylation and Acetylation of 15-Hydroxyanandamide Modulate its Interaction with the Endocannabinoid System.</title>
            <link>http://www.medworm.com/index.php?rid=3212776&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096328%26dopt%3DAbstract</link>
            <description>Authors: Amadio D, Fezza F, Catanzaro G, Incani O, van Zadelhoff G, Agr&amp;#xF2; AF, Maccarrone M
    The biological activity of endocannabinoids like anandamide (AEA) and 2-arachidonoylglycerol (2-AG) is subjected in vivo to a &quot;metabolic control&quot;, exerted mainly by catabolic enzymes. AEA is inactivated by fatty acid amide hydrolase (FAAH), that is inhibited competitively by hydroxyanandamides (HAEAs) generated from AEA by lipoxygenase activity. Among these derivatives, 15-HAEA has been shown to be an effective (K(i) approximately 0.6 muM) FAAH inhibitor, that blocks also type-1 cannabinoid receptor (CB1R) but not other components of the &quot;endocannabinoid system (ECS)&quot;, like the AEA transporter (AMT) or CB2R. Here, we extended the study of the effect of 15-HAEA on the AEA synthetase (NAPE-PLD)...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3212776</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3212776</guid>        </item>
        <item>
            <title>Expanding the role of Src and protein tyrosine phosphatases balance in modulating osteoblast metabolism: lessons from mice.</title>
            <link>http://www.medworm.com/index.php?rid=3194540&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20083150%26dopt%3DAbstract</link>
            <description>Authors: Zambuzzi WF, Milani R, Teti A
    The widespread nature of protein phosphorylation/dephosphorylation underscores its key role in cell signaling metabolism, growth and differentiation. Tyrosine phosphorylation of cytoplasmic proteins is a critical event in the regulation of intracellular signaling pathways activated by external stimuli. An adequate balance in protein phosphorylation is a major factor in the regulation of osteoclast and osteoblast activities involved in bone metabolism. However, although phosphorylation is widely recognized as an important regulatory pathway in skeletal development and maintenance, the mechanisms involved are not fully understood. Among the putative protein tyrosine kinases (ptk) and protein tyrosine phosphatases (ptp) involved in this phenomenon th...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3194540</comments>
            <pubDate>Fri, 15 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3194540</guid>        </item>
        <item>
            <title>Group VIA Ca(2+)-Independent Phospholipase A(2) (iPLA(2)beta) and its role in beta-cell Programmed Cell Death.</title>
            <link>http://www.medworm.com/index.php?rid=3194539&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20083151%26dopt%3DAbstract</link>
            <description>Authors: Lei X, Barbour SE, Ramanadham S
    Activation of phospholipases A(2) (PLA(2)s) leads to the generation of biologically active lipid mediators that can affect numerous cellular events. The Group VIA Ca(2+)-independent PLA(2), designated iPLA(2)(R), is active in the absence of Ca(2+), activated by ATP, and inhibited by the bromoenol lactone suicide inhibitor (BEL). Over the past 10-15 years, studies using BEL have demonstrated that iPLA(2)beta participates in various biological processes and the recent availability of mice in which iPLA(2)beta expression levels have been genetically-modified are extending these findings. Work in our laboratory suggests that iPLA(2)(R) activates a unique signaling cascade that promotes beta-cell apoptosis. This pathway involves iPLA(2)(R) dependent ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3194539</comments>
            <pubDate>Fri, 15 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3194539</guid>        </item>
        <item>
            <title>Characterization of a new periplasmic single-domain rhodanese encoded by a sulfur-regulated gene in a hyperthermophilic bacterium Aquifex aeolicus.</title>
            <link>http://www.medworm.com/index.php?rid=3164279&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20060433%26dopt%3DAbstract</link>
            <description>Authors: Giuliani MC, Jourlin-Castelli C, Leroy G, Hachani A, Giudici-Orticoni MT
    Rhodaneses (thiosulfate cyanide sulfurtransferases) are enzymes involved in the production of the sulfur in sulfane form, which has been suggested to be the relevant biologically active sulfur species. Rhodanese domains occur in the three major domains of life. We have characterized a new periplasmic single-domain rhodanese from a hyperthermophile bacterium, Aquifex aeolicus, with thiosulfate:cyanide transferase activity, Aq-1599. The oligomeric organization of the enzyme is stabilized by a disulfide bridge. To date this is the first characterization from a hyperthermophilic bacterium of a periplasmic sulfurtransferase with a disulfide bridge. The aq-1599 gene belongs to an operon that also contains a gen...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3164279</comments>
            <pubDate>Thu, 07 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3164279</guid>        </item>
        <item>
            <title>Mechanisms of triplex DNA-mediated inhibition of transcription initiation in cells.</title>
            <link>http://www.medworm.com/index.php?rid=3139537&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20045441%26dopt%3DAbstract</link>
            <description>Authors: Jain A, Magistri M, Napoli S, Carbone GM, Catapano CV
    Triplex-forming oligonucleotides (TFOs) are attractive tools to control gene expression at the transcriptional level. This anti-gene approach has proven to be successful in various experimental settings. However, the mechanisms leading to transcriptional repression in cells have not been fully investigated yet. Here, we examined the consequence of triplex DNA formation on the binding of transcriptional activators, co-activators and RNA Polymerase II to the ets2 gene promoter using chromatin immunoprecipitation assays. The triplex target sequence was located approximately 40-bp upstream of the transcription start site (TSS) and overlapped an Sp1 binding site relevant for ets2 transcription. We found that the ets2-TFO prevent...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3139537</comments>
            <pubDate>Thu, 31 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3139537</guid>        </item>
        <item>
            <title>Riboregulators in kidney development and function.</title>
            <link>http://www.medworm.com/index.php?rid=3139539&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20045037%26dopt%3DAbstract</link>
            <description>Authors: Setyowati KD, Coghlan WE, Bertram J, Jeyaseelan K
    The discovery of microRNAs has brought in another level of intricacy in gene regulation. These microRNAs are small non-coding RNAs that have dual ability to act as repressors or inducers of gene activity. MicroRNAs have been implicated in a wide spectrum of biological processes and their expressions have been found to be dysregulated in several diseases. Recently, microRNAs have emerged as a new area of interest in renal development and pathology. MicroRNA profilings have revealed a number of microRNAs that are specific to the kidney or restricted to certain regions of the organ suggesting possible exclusive roles therein. Recently, knockout studies have shown that these riboregulators are critical for normal renal growth and f...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3139539</comments>
            <pubDate>Wed, 30 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3139539</guid>        </item>
        <item>
            <title>IL-17A suppresses the expression of bone resorption-related proteinases and osteoclast differentiation via IL-17RA or IL-17RC receptors in RAW264.7 cells.</title>
            <link>http://www.medworm.com/index.php?rid=3139538&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20045440%26dopt%3DAbstract</link>
            <description>Authors: Kitami S, Tanaka H, Kawato T, Tanabe N, Katono-Tani T, Zhang F, Suzuki N, Yonehara Y, Maeno M
    Interleukin-17 (IL-17) is produced exclusively by activated T cells and neutrophils, and stimulates osteoclastic bone resorption via osteoblasts by inducing the expression of &quot;receptor activator of NF-small ka, CyrillicB (RANK) ligand&quot; (RANKL). However, the direct effects of IL-17 on the differentiation of osteoclast precursors into osteoclasts and on the function of osteoclasts have not been clarified. Therefore, we examined the effects of IL-17A on the differentiation of osteoclast precursors using RAW264.7 cells and also on the expression of carbonic anhydrase II (CA II), cathepsin K, matrix metalloproteinases-9 (MMP-9), RANK, c-fms, and IL-17 receptors in these cells. The cells we...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3139538</comments>
            <pubDate>Wed, 30 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3139538</guid>        </item>
        <item>
            <title>Protective effect of post-ischemic treatment with trans-resveratrol on cytokine production and neutrophil recruitment by rat liver.</title>
            <link>http://www.medworm.com/index.php?rid=3129982&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20036306%26dopt%3DAbstract</link>
            <description>This study investigated the early anti-inflammatory effect of trans-resveratrol (T-res) and its consequences on the late self-aggravating inflammatory process in liver ischemia-reperfusion (I/R). Partial hepatic ischemia was initiated in rats for 1h and T-res (0.02 and 0.2mg/kg) was administered intravenously 5min before starting reperfusion for 3h. Plasma levels of aminotransferases and cytokines (tumour necrosis factor (TNF)-alpha, interleukin (IL)-1beta, IL-6) and hepatic neutrophil recruitment were assessed. Hepatic expression of stress protein (heat-shock protein (HSP-70), heme oxygenase-1(HO-1)) and cytokine (TNF-alpha, IL-1beta, keratinocyte chemoattractant (KC)) mRNA was investigated. I/R caused an increase in aminotransferase levels and increased polymorphonuclear cell infiltratio...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3129982</comments>
            <pubDate>Wed, 23 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3129982</guid>        </item>
        <item>
            <title>Which alkylglycerols from shark liver oil have anti-tumour activities ?</title>
            <link>http://www.medworm.com/index.php?rid=3129981&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20036307%26dopt%3DAbstract</link>
            <description>Authors: Deniau AL, Mosset P, Le Bot D, Legrand AB
    Alkylglycerols (alkyl-Gro) are ether lipids abundant in shark liver oil (SLO), and oral SLO or alkyl-Gro mix from this source have several in vivo biological activities including stimulation of haematopoiesis an immunological defences, or anti-tumour and anti-metastasis activities in vivo. Composition of natural alkyl-Gro mix contains several alkyl-Gro varying by chain length and unsaturation, and individual anti-tumour activity of each molecule present in natural mix remained unknown. We synthesized six prominent constituents of natural alkyl-Gro mix, namely 12:0, 14:0 16:0, 18:0, 16:1n-7, and 18:1n-9 alkyl-Gro. Using an in vivo model of grafted tumour in mice (3LL cells), we studied and compared the oral anti-tumour and anti-metastas...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3129981</comments>
            <pubDate>Wed, 23 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3129981</guid>        </item>
        <item>
            <title>Profiling gene expression of whole cytochrome P450 superfamily in human bronchial and peripheral lung tissues: Differential expression in non-small cell lung cancers.</title>
            <link>http://www.medworm.com/index.php?rid=3122553&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034539%26dopt%3DAbstract</link>
            <description>This study highlights (i) interindividual variations in lung expression for some CYPs, (ii) different CYP expression patterns between bronchial mucosa and pulmonary parenchyma, that indicate distinctive susceptibility of these tissues toward the deleterious effects of inhaled chemical toxicants and carcinogens, (iii) high intertumoral variability, that could have major implications on lung tumor response to anti-cancer drugs.
    PMID: 20034539 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122553</comments>
            <pubDate>Mon, 21 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3122553</guid>        </item>
        <item>
            <title>New insights into the mechanism of dihydrodipicolinate synthase using isothermal titration calorimetry.</title>
            <link>http://www.medworm.com/index.php?rid=3112116&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20025926%26dopt%3DAbstract</link>
            <description>Authors: Muscroft-Taylor AC, Soares da Costa TP, Gerrard JA
    Thermodynamic binding information, obtained via isothermal titration calorimetry (ITC), provides new insights into the binding of substrates, and of allosteric inhibitor interactions of dihydrodipicolinate synthase (DHDPS) from Escherichia coli. DHDPS catalyses the first committed step in (S)-lysine biosynthesis: the Schiff-base mediated aldol condensation of pyruvate with (S)-aspartate semi-aldehyde. Binding studies indicate that pyruvate is a weak binder (0.023 mM) but that (S)-ASA does not interact with the enzyme in the absence a Schiff-base with pyruvate. These results support the assignment of ping pong catalytic mechanism in which enthalpically driven Schiff-base formation (DeltaH = -44.5 +/- 0.1 kJ mol(-1)) provides th...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3112116</comments>
            <pubDate>Wed, 16 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3112116</guid>        </item>
        <item>
            <title>Isolation of an acidic phospholipase A(2) from the venom of the snake Bothrops asper of Costa Rica: Biochemical and toxicological characterization.</title>
            <link>http://www.medworm.com/index.php?rid=3112115&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20026168%26dopt%3DAbstract</link>
            <description>In this study, an acidic enzyme (BaspPLA(2)-II) was isolated from the venom of Bothrops asper (Pacific region of Costa Rica) and characterized. BaspPLA(2)-II is monomeric, with a mass of 14,212 +/- 6 Da and a pI of 4.9. Its complete sequence of 124 amino acids was deduced through cDNA and protein sequencing, showing that it belongs to the Asp49 group of catalytically active enzymes. In vivo and in vitro assays demonstrated that BaspPLA(2)-II, in contrast to the basic Asp49 counterparts present in the same venom, lacks myotoxic, cytotoxic, and anticoagulant activities. BaspPLA(2)-II also differed from other acidic PLA(2)s described in Bothrops spp. venoms, as it did not show hypotensive and anti-platelet aggregation activities. Furthermore, this enzyme was not lethal to mice at intravenous ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3112115</comments>
            <pubDate>Wed, 16 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3112115</guid>        </item>
        <item>
            <title>Stabilization of transcription factor Nrf2 by tBHQ prevents oxidative stress-induced amyloid beta formation in NT2N neurons.</title>
            <link>http://www.medworm.com/index.php?rid=3112114&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20026169%26dopt%3DAbstract</link>
            <description>Authors: Eftekharzadeh B, Maghsoudi N, Khodagholi F
    Alzheimer's disease (AD) a progressive neurodegenerative disorder of later life, is characterized by brain deposition of amyloid beta-protein (Abeta) plaques, accumulation of intracellular neurofibrillatory tangles, synaptic loss and neuronal cell death. There is significant evidence that oxidative stress is a critical event in the pathogenesis of AD. In the present study Abeta formation was induced in NT2N neurons, one of the most appropriate cell line models in AD. Our results indicate that oxidative stress resulting from the treatment of H(2)O(2)/FeSO4 and/or 4-hydroxy-2-noenal (HNE) can be inhibited in the presence of tBHQ, a known inducer of nuclear factor erythroid 2-related factor 2 (Nrf2) in NT2N neurons and can therefore be u...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3112114</comments>
            <pubDate>Wed, 16 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3112114</guid>        </item>
        <item>
            <title>Cloning and characterization of the first amphibian bradykinin gene.</title>
            <link>http://www.medworm.com/index.php?rid=3112117&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20025925%26dopt%3DAbstract</link>
            <description>Authors: Chen M, Che Q, Wang X, Li J, Yang H, Li D, Zhang K, Lai R
    More than ten bradykinin-related peptides and their cDNAs have been identified from amphibians, but their genes are unknown. In present study, four cDNAs encoding one, two, four and six copies of bradykinin-related peptides were cloned from the frog (Odorrana grahami) skin cDNA library, respectively. Three bradykinin-related peptides (bradykinin, Thr6-bradykinin, Leu5Thr6-bradykinin) were deduced from these four cDNA sequences. Based on the cDNA sequence, the gene sequence encoding an amphibian bradykinin-related peptide from O. grahami was determined. It is composed of 7481 base pairs including two exons and two introns. The first exon codes signal peptide and the second exon codes acidic spacer peptide and Thr6-bradyk...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3112117</comments>
            <pubDate>Tue, 15 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3112117</guid>        </item>
        <item>
            <title>Lipidomic Approaches to the Study of Phospholipase A(2)-regulated Phospholipid Fatty Acid Incorporation and Remodeling.</title>
            <link>http://www.medworm.com/index.php?rid=3072394&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19969040%26dopt%3DAbstract</link>
            <description>Authors: Balgoma D, Montero O, Balboa MA, Balsinde J
    The distribution of fatty acids among cellular glycerophospholipids is finely regulated by the CoA-dependent acylation of lysophospholipids followed by transacylation reactions. Arachidonic acid is the fatty acid precursor of a wide family of bioactive compounds called the eicosanoids, with key roles in innate immunity and inflammation. Because availability of free AA constitutes a rate-limiting step in the generation of eicosanoids by mammalian cells, many studies have been devoted to characterize the processes of arachidonate liberation from phospholipids by phospholipase A(2)s and its re-incorporation and further remodeling back into phospholipids by acyltransferases and transacylases. These studies have traditionally been conduct...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3072394</comments>
            <pubDate>Fri, 04 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3072394</guid>        </item>
        <item>
            <title>Sodium permeability and sensitivity induced by mutations in the selectivity filter of the KcsA channel towards Kir channels.</title>
            <link>http://www.medworm.com/index.php?rid=3066269&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19962419%26dopt%3DAbstract</link>
            <description>Authors: Raja M, Vales E
    The bacterial potassium (K(+)) channel KcsA provides an attractive model system to study ion permeation behaviour in a selective K(+)-channel. We changed residue at the N-terminal end of the selectivity filter of KcsA (T74V) to its counterpart in inwardly rectifying K(+)-channels (Kir). The tetramer was found to be stable as unmodified KcsA. Under symmetrical and asymmetrical conditions, Na(+) increased the inward current in the virtual absence of K(+) however outward currents were nearly abolished which could be recovered upon internal K(+) addition. Na(+) also drastically increased the channel open time either in the presence or virtual absence of K(+). Furthermore, the T74V mutation decreased the internal Ba(2+) affinity of the channel possibly by binding to...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3066269</comments>
            <pubDate>Wed, 02 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3066269</guid>        </item>
        <item>
            <title>Interaction analysis of TcrX/Y two component system from Mycobacterium tuberculosis.</title>
            <link>http://www.medworm.com/index.php?rid=3066261&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19962420%26dopt%3DAbstract</link>
            <description>Authors: Bhattacharya M, Biswas A, Das AK
    TcrX/Y is one of the twelve two component system (TCS) present in Mycobacterium tuberculosis. We have investigated the TcrX/Y interaction by in silico studies, pull down assay, radioactive phosphotransfer, surface plasmon resonance as well as crosstalk analysis of TcrY with TcrA - a non-cognate response regulator. Sequence alignment of TcrY with other histidine kinases revealed His256 as the residue responsible for autophosphorylation. The modeled structure of TcrX/Y was docked with each other by GRAMM-X revealing the interaction of TcrY/His256 with TcrX/Asp54. TcrY dimerization via the formation of four helix bundle was also observed by protein-protein docking. Autophosphorylation of TcrY has been observed followed by the phosphate transfer fr...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3066261</comments>
            <pubDate>Wed, 02 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3066261</guid>        </item>
        <item>
            <title>Overexpression of a wheat jasmonate-regulated lectin increases pathogen resistance.</title>
            <link>http://www.medworm.com/index.php?rid=3061627&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19958808%26dopt%3DAbstract</link>
            <description>Authors: Ma QH, Tian B, Li YL
    Jasmonates are known to induce the transcriptional activation of plant defense genes, which leads to the production of jasmonate-regulated proteins (JRP). We previously cloned and characterized a novel jacalin-like lectin gene (Ta-JA1) from wheat (Triticum aestivum L.), which codes a modular JRP with disease response and jacalin-related lectin (JRL) domains and is present only in the Gramineae family. The function of this protein is still unclear. Phylogenetic analysis indicated that Ta-JA1 and related proteins from cereals grouped together, which diverged from JRL with an additional N-terminal disease response domain. The recombinant Ta-JA1 proteins agglutinated rabbit erythrocytes, and this hemagglutination activity was preferentially inhibited by mannos...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3061627</comments>
            <pubDate>Mon, 30 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3061627</guid>        </item>
        <item>
            <title>Differential behaviour of Pseudomonas sp. 42A2 LipC, a lipase showing greater versatility than its counterpart LipA.</title>
            <link>http://www.medworm.com/index.php?rid=3049000&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19944735%26dopt%3DAbstract</link>
            <description>Authors: Bofill C, Prim N, Mormeneo M, Manresa A, Javier Pastor FI, Diaz P
    Growth of Pseudomonas sp. 42A2 on oleic acid releases polymerized hydroxy-fatty acids as a result of several enzymatic conversions that could involve one or more lipases. To test this hypothesis, the lipolytic system of strain Pseudomonas sp. 42A2 was analyzed, revealing the presence of at least an intracellular carboxylesterase and a secreted lipase. Consensus primers derived from a conserved region of bacterial lipase subfamilies I.1 and I.2 allowed isolation of two secreted lipase genes, lipA and lipC, highly homologous to those of Pseudomonas aeruginosa PAO1. Homologous cloning of the isolated lipA and lipC genes was performed in Pseudomonas sp. 42A2 for LipA and LipC over-expression. The overproduced lipase...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3049000</comments>
            <pubDate>Wed, 25 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3049000</guid>        </item>
        <item>
            <title>A host-specific factor is necessary for efficient folding of the autotransporter plasmid-encoded toxin.</title>
            <link>http://www.medworm.com/index.php?rid=3049001&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19944129%26dopt%3DAbstract</link>
            <description>Authors: Nemec KN, Scaglione P, Navarro-Garc&amp;#xED;a F, Huerta J, Tatulian SA, Teter K
    Autotransporters are the most common virulence factors secreted from Gram-negative pathogens. Until recently, autotransporter folding and outer membrane translocation were thought to be self-mediated events that did not require accessory factors. Here, we report that two variants of the autotransporter plasmid-encoded toxin are secreted by a lab strain of Escherichia coli. Biophysical analysis and cell-based toxicity assays demonstrated that only one of the two variants was in a folded, active conformation. The misfolded variant was not produced by a pathogenic strain of enteroaggregative E. coli and did not result from protein overproduction in the lab strain of E. coli. Our data suggest a host-speci...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3049001</comments>
            <pubDate>Tue, 24 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3049001</guid>        </item>
        <item>
            <title>Neurotensin expression and outcome of malignant pleural mesothelioma.</title>
            <link>http://www.medworm.com/index.php?rid=3031383&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19932148%26dopt%3DAbstract</link>
            <description>Authors: Alifano M, Loi M, Camilleri-Broet S, Dupouy S, R&amp;#xE9;gnard JF, Forgez P
    Malignant pleural mesothelioma is a frequently fatal disease and the impact of available treatments is globally poor. Identification of new prognostic factors would help in the understanding of disease progression and, possibly, patient management. Here, we evaluate the prognostic impact of the neurotensin (NTS) and its cognate receptor (NTSR1) known for mediating cellular proliferation, survival, invasiveness, and mobility. We studied a series of 52 consecutive patients with epithelioid malignant mesothelioma undergoing management with curative intent, by immunochemistry for the expression of NTS and NTSR1. Specimens were scored as 0, 1, or 2 for less than 10%, between 10 and 50%, or more than 50% of NTS...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3031383</comments>
            <pubDate>Thu, 19 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3031383</guid>        </item>
        <item>
            <title>Translation factor LepA contributes to tellurite resistance in Escherichia coli but plays no apparent role in the fidelity of protein synthesis.</title>
            <link>http://www.medworm.com/index.php?rid=3019407&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19925844%26dopt%3DAbstract</link>
            <description>Authors: Shoji S, Janssen BD, Hayes CS, Fredrick K
    LepA is a translational GTPase highly conserved in bacterial lineages. While it has been shown that LepA can catalyze reverse ribosomal translocation in vitro, the role of LepA in the cell remains unclear. Here, we show that deletion of the lepA gene (DeltalepA) in E. coli causes hypersensitivity to potassium tellurite and penicillin G, but has no appreciable effect on growth under many other conditions. DeltalepA does not increase miscoding or frameshifting errors under normal or stress conditions, indicating that LepA does not contribute to the fidelity of translation. Overexpression of LepA interferes with tmRNA-mediated peptide tagging and A-site mRNA cleavage, suggesting that LepA is a bona fide translation factor that can act on ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3019407</comments>
            <pubDate>Mon, 16 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3019407</guid>        </item>
        <item>
            <title>Recognition intensities of submolecular structures, mammalian glyco-structural units, ligand cluster and polyvalency in abrin-a-carbohydrate interactions.</title>
            <link>http://www.medworm.com/index.php?rid=3000615&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19913595%26dopt%3DAbstract</link>
            <description>In this study, roles of mammalian glyco-structural units, ligand clusters and polyvalency in abrin-a recognition were comprehensively analyzed by enzyme-linked lectinosorbent binding and inhibition assays. The results indicate that: (i) this toxin prefers oligosaccharides having alpha-anomer of galactose (Gal) at the non-reducing terminal than the corresponding beta-anomer; (ii) Galalpha1-3Galalpha1- (B(alpha)), Galalpha1-4Gal (E), Galbeta1-3GalNAc (T) and Galbeta1-3/4GlcNAc (I/II) related oligosaccharides were the active glyco-structural units; (iii) tri-antennary II(beta), prepared from N-glycan of asialo fetuin, played a dominant role in recognition; (iv) many high-density polyvalent I(beta)/II(beta) and E(beta) glycotopes enhanced the reactivity; (v) the carbohydrate recognition domain...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3000615</comments>
            <pubDate>Wed, 11 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3000615</guid>        </item>
        <item>
            <title>Characterization of the Structure of the Phosphoprotein of Chandipura Virus, a Negative Stranded RNA Virus Probing Intratryptophan Energy Transfer Using Single and Double Tryptophan Mutants.</title>
            <link>http://www.medworm.com/index.php?rid=2977874&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19895867%26dopt%3DAbstract</link>
            <description>Authors: Mukhopadhyay S, Maity SS, Roy A, Chattopadhyay D, Ghosh KS, Dasgupta S, Ghosh S
    The phosphoprotein (P protein) of Chandipura virus (CHPV), a negative stranded RNA virus, is involved in both transcription and replication phases of the viral life cycle. The two Tryptophan (Trp) residues of CHPV, located at 105 and 135 respectively and two single Trp mutants W135F and W105F and a double Trp mutant W135F/W105F have been characterized by steady state and time resolved fluorescence and phosphorescence at 298K and 77K. Results indicate that Trp135 is more buried with less polar and more hydrophobic environment whereas the Trp105 is solvent exposed. Quantum yields (capital EF, Cyrillic) suggest that the singlet-singlet (S&amp;lt;--&amp;gt;S) non radiative energy transfer (ET) from the Trp135 ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2977874</comments>
            <pubDate>Tue, 03 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2977874</guid>        </item>
        <item>
            <title>Molecular size hyaluronan differently modulates toll-like receptor-4 in LPS-induced inflammation in mouse chondrocytes.</title>
            <link>http://www.medworm.com/index.php?rid=2959881&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19879319%26dopt%3DAbstract</link>
            <description>Authors: Campo GM, Avenoso A, Campo S, D'Ascola A, Nastasi G, Calatroni A
    Hyaluronan (HA) action depends upon its molecular size. Low molecular weight HA elicits pro-inflammatory responses by modulating the toll-like receptor-4 (TLR-4) or by activating the nuclear factor kappa B (NF-kB). In contrast, high molecular weight HA manifests an anti-inflammatory effect via CD receptors and by inhibiting NF-kB activation. Lipopolysaccharide (LPS) -mediated activation of TLR-4 complex induces the myeloid differentiation primary-response protein (MyD88) and the tumor necrosis factor receptor-associated factor-6 (TRAF-6), and ends with the liberation of NF-kB/Rel family members. The aim of this study was to investigate the influence of HA at different MWs (low, medium, high) on TLR-4 modulation i...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2959881</comments>
            <pubDate>Fri, 30 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2959881</guid>        </item>
        <item>
            <title>Phosphorylated intermediate of the ouabain-insensitive, Na(+)-stimulated ATPase in rat kidney cortex and rainbow trout gills.</title>
            <link>http://www.medworm.com/index.php?rid=2959880&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19883725%26dopt%3DAbstract</link>
            <description>Authors: Ventrella V, Elvir JR, Borgatti AR, Trigari G, Proverbio T, Pagliarani A, Trombetti F, Pirini M, Mar&amp;#xED;n R, Proverbio F
    Several tissues from different animals, including the rat kidney and the fresh water rainbow trout gills, show an ouabain-insensitive, furosemide-sensitive, Na(+)-stimulated ATPase activity, which has been associated with the active control of the cell volume. This Na-ATPase is Mg(2+) dependent and it is inhibited by vanadate, which can be taken as an indication that this enzyme is a P-type ATPase. The P-type ATPases are known to form a phosphorylated intermediate during their catalytic cycle, where the phosphate binds an aspartyl residue at the enzyme's substrate site. In the current study, we partially characterized the phosphorylated intermediate of the...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2959880</comments>
            <pubDate>Fri, 30 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2959880</guid>        </item>
        <item>
            <title>Astacin-like metalloproteases are a gene family of toxins present in the venom of different species of the brown spider (genus Loxosceles).</title>
            <link>http://www.medworm.com/index.php?rid=2959882&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19879318%26dopt%3DAbstract</link>
            <description>This study identified the existence of gene family of astacin-like toxins in the venoms of brown spiders and raises the possibility that these molecules are involved in the deleterious effects triggered by the venom.
    PMID: 19879318 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2959882</comments>
            <pubDate>Thu, 29 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2959882</guid>        </item>
        <item>
            <title>Kinetic properties and specificity of trimeric plasmodium falciparum and human dutpases.</title>
            <link>http://www.medworm.com/index.php?rid=2959884&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19879316%26dopt%3DAbstract</link>
            <description>Authors: Quesada-Soriano I, Casas-Solvas JM, Recio E, Ruiz-P&amp;#xE9;rez LM, Vargas-Berenguel A, Gonz&amp;#xE1;lez-Pacanowska D, Garc&amp;#xED;a-Fuentes L
    Deoxyuridine 5'-triphosphate nucleotidohydrolase (dUTPase, EC 3.6.1.23) catalyzes the hydrolysis of dUTP to dUMP and pyrophosphate, and plays important roles in nucleotide metabolism and DNA replication. Hydrolysis of other nucleotides similar in structure to dUTP would be physiologically negative and therefore high substrate specificity is essential. Binding and hydrolysis of nucleotides different to dUTP by the dUTPases from Plasmodium falciparum (PfdUTPase) and human (hdUTPase) was evaluated by applying isothermal titration calorimetry (ITC). The ribo and deoxyribonucleoside triphosphates dGTP, dATP, dCTP, dTTP, UTP, FdUTP and IdUTP have bee...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2959884</comments>
            <pubDate>Wed, 28 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2959884</guid>        </item>
        <item>
            <title>Design of Proton-fueled Tweezers for Controlled, Multi-function DNA-based Molecular Device.</title>
            <link>http://www.medworm.com/index.php?rid=2959883&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19879317%26dopt%3DAbstract</link>
            <description>Authors: Song G, Chen M, Chen C, Wang C, Hu D, Ren J, Qu X
    A novel multifunctional, proton fueled DNA tweezers has been constructed. Starting from simple conformation change of i-motif DNA, the nanodevice can accomplish movements such as repeatedly capture or release target DNA and protein. The DNA tweezers, driven by the solution pH without the need of injecting external energy, are robust and highly reversible with the responses of 1-2 orders of magnitude faster than the DNA fuelled machine, and does not accumulate duplex waste products to poison the system. Our work has demonstrated the successful combination of the operating principles of DNA-based nanomechnical device with the unique molecular recognition properties of DNA, which we believed could open an exciting avenue in the de...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2959883</comments>
            <pubDate>Wed, 28 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2959883</guid>        </item>
        <item>
            <title>The C-terminal amphipathic alpha-helix of Pseudomonas aeruginosa PelC outer membrane protein is required for its function.</title>
            <link>http://www.medworm.com/index.php?rid=2935342&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19853003%26dopt%3DAbstract</link>
            <description>Authors: Kowalska K, Soscia C, Combe H, Vasseur P, Voulhoux R, Filloux A
    Pseudomonas aeruginosa is an opportunistic pathogen, which causes numerous infections and can adopt a versatile lifestyle. During chronic infection, P. aeruginosa becomes established as a bacterial community known as a biofilm. Biofilm formation results from the production of a matrix mainly comprised of exopolysaccharides. P. aeruginosa possesses several gene clusters which contribute to the formation of the matrix, including the pel genes. Among the pel genes, pelC encodes an outer membrane protein, which may serve as a transporter of polysaccharide to the bacterial cell surface. Whereas outer membrane proteins usually display an amphipathic beta-barrel fold, we show that PelC requires a C-terminal amphipathic a...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2935342</comments>
            <pubDate>Thu, 22 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2935342</guid>        </item>
        <item>
            <title>Alterations of matrix metalloproteinases, gastric mucin and prostaglandin E(2) levels by pectic polysaccharide of swallow root (Decalepis hamiltonii) during ulcer healing.</title>
            <link>http://www.medworm.com/index.php?rid=2935341&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19853004%26dopt%3DAbstract</link>
            <description>Authors: Srikanta BM, Sathisha UV, Dharmesh SM
    Gastric ulcer is a multi-step disease caused due to imbalance between mucosal defense and aggressive factors. Available anti-ulcer drugs although effective at various steps of ulcer pathogenesity, pose adverse effects. Pectic polysaccharide (SRPP) from swallow root (Decalepis hamiltonii) - previously shown to possess ulcer preventive effect against swim stress and ethanol induced gastric ulcers. In the current study, alteration of matrix metalloproteinases, gastric mucin and prostaglandin E(2) levels during polysaccharide mediated ulcer healing was determined in acetic acid induced gastric ulcer model in Wistar albino rats. Results indicated the potential ulcer healing effect of SRPP as evidenced by approximately 90% reduction in ulcer ind...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2935341</comments>
            <pubDate>Thu, 22 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2935341</guid>        </item>
        <item>
            <title>Maximum rrn promoter activity in Escherichia coli at saturating concentrations of free RNA polymerase.</title>
            <link>http://www.medworm.com/index.php?rid=2909773&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19835927%26dopt%3DAbstract</link>
            <description>Authors: Ehrenberg M, Dennis PP, Bremer H
    During fast growth, the rrn P1 promoters of Escherichia coli operate at their maximum strength, but below their maximum activity (V(max)), since they are not saturated with RNA polymerase. Since higher concentrations of free RNA polymerase are expected to be found in strains carrying rrn deletions, we have analyzed reported electron micrographs of rrn operons from rrn deletion strains growing at maximal rates (at 37 degrees C) in LB medium [1]. We conclude that, in a strain with four of the seven rrn operons inactivated by partial deletions, transcripts are initiated at rrn P1 promoters 1.6-fold more rapidly than in the wild-type strain and the entirety of the rrn operon is transcribed at a 1.5-fold higher average elongation rate due to shorten...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2909773</comments>
            <pubDate>Wed, 14 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2909773</guid>        </item>
        <item>
            <title>Rottlerin induces Heme Oxygenase-1(HO-1) up-regulation through reactive oxygen species (ROS) dependent and PKC delta-independent pathway in human colon cancer HT29 cells.</title>
            <link>http://www.medworm.com/index.php?rid=2902046&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19833168%26dopt%3DAbstract</link>
            <description>In this study, the effect of rottlerin, a putative PKC delta inhibitor, on HO-1 expression in HT29 human colon cancer cells was investigated. Treatment with rottlerin induced HO-1 at both protein and mRNA levels in a dose- and time-dependent manner. Rottlerin-mediated HO-1 induction was abrogated in the presence of N-acetylcysteine (NAC) and glutathione (GSH). Rottlerin induced nuclear translocation of NF-E2-related factor 2 (Nrf2) and increased antioxidant response element (ARE)-driven transcriptional activity. Additionally, rottlerin activated p38 mitogen-activated protein kinase (MAPK) and ERK. The pharmacological inhibition of ERK and p38 MAPK inhibited rottlerin-induced HO-1 up-regulation. However, suppression of protein kinase C delta (PKC delta) expression by siRNA or overexpression...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2902046</comments>
            <pubDate>Sun, 11 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2902046</guid>        </item>
        <item>
            <title>Identification of the reactive cysteine residues in yeast dipeptidyl peptidase III.</title>
            <link>http://www.medworm.com/index.php?rid=2895241&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19825391%26dopt%3DAbstract</link>
            <description>Authors: Jaj&amp;#x10D;anin-Jozi&amp;#x107; N, Deller S, Pavkov T, Macheroux P, Abrami&amp;#x107; M
    Dipeptidyl peptidases III (DPPs III) form a distinct metallopeptidase family characterized by the unique HEXXGH motif. High susceptibility to inactivation by organomercurials suggests the presence of a reactive cysteine residue(s) in, or close to, their active site. Yeast DPP III contains five Cys, none of which is absolutely conserved within the family. In order to identify reactive residue(s), site-directed mutagenesis on yeast His(6)-tagged DPP III was employed to substitute specifically all five cysteine residues to serine. The variant enzymes thus obtained were enzymatically active and showed an overall structure not greatly affected by the mutations as judged by circular dichroism. Analysis by...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2895241</comments>
            <pubDate>Fri, 09 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2895241</guid>        </item>
        <item>
            <title>Structural and functional evaluation of three well-conserved serine residues in tobacco acetohydroxyacid synthase.</title>
            <link>http://www.medworm.com/index.php?rid=2895240&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19825392%26dopt%3DAbstract</link>
            <description>Authors: Yoon MY, Gedi V, Kim J, Park Y, Kim DE, Park EH, Choi JD
    The first step in the common pathway for the biosynthesis of branched-chain amino acids (BCAA) is catalyzed by acetohydroxyacid synthase (AHAS). The roles of three well-conserved serine residues (S167, S506, and S539) in tobacco AHAS were determined using site-directed mutagenesis. The mutations S167F and S506F were found to be inactive and abolished the binding affinity for cofactor FAD. The Far-UV CD spectrum of the inactive mutants was similar to that of wild-type enzyme, indicating no major conformational changes in the secondary structure. However, the active mutants, S167R, S506A, S506R, S539A, S539F and S539R, showed lower specific activities. Further, a homology model of tobacco AHAS was generated based on the cr...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2895240</comments>
            <pubDate>Fri, 09 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2895240</guid>        </item>
        <item>
            <title>Interaction between lanthanum ion and horseradish peroxidase in vitro.</title>
            <link>http://www.medworm.com/index.php?rid=2895242&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19822184%26dopt%3DAbstract</link>
            <description>Authors: Wang L, Lu A, Lu T, Ding X, Huang X
    The interaction between lanthanum ion (La(3+)) and horseradish peroxidase (HRP) in vitro was investigated using a combination of biophysical and biochemical methods. When the molar ratio of La(3+) and HRP is low, it was found that the interaction between La(3+) and HRP mainly depends on the electrostatic attraction, van der waals force and hydrogen bond etc. Thus, the interaction is weak and the La-HRP complex can not be formed in vitro. As expected, the interaction can change the conformation of HRP molecule, leading to the increase in the non-planarity of the porphyrin ring in the heme group of HRP molecule, and then in the exposure degree of the active center, Fe(III) of the porphyrin ring of HRP molecule. Therefore, the catalytic activit...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2895242</comments>
            <pubDate>Thu, 08 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2895242</guid>        </item>
        <item>
            <title>The membrane-bound mucins: From cell signalling to transcriptional regulation and expression in epithelial cancers.</title>
            <link>http://www.medworm.com/index.php?rid=2887307&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19818375%26dopt%3DAbstract</link>
            <description>Authors: Jonckheere N, Van Seuningen I
    The membrane-bound mucins belong to an ever-increasing family of O-glycoproteins. Based on their structure and localization at the cell surface they are thought to play important biological roles in cell-cell and cell-matrix interactions, in cell signalling and in modulating biological properties of cancer cells. Among them, MUC1 and MUC4 mucins are best characterized. Their altered expression in cancer (overexpression in the respiratory, gastro-intestinal, urogenital and hepato-biliary tracts) indicates an important role for these membrane-bound mucins in tumour progression, metastasis, cancer cell resistance to chemotherapeutics drugs and as specific markers of epithelial cancer cells. Some mechanisms responsible for MUC1 and MUC4 role in tumour...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2887307</comments>
            <pubDate>Wed, 07 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2887307</guid>        </item>
        <item>
            <title>Increasing the synthesis/hydrolysis ratio of aminoacylase 1 by site-directed mutagenesis.</title>
            <link>http://www.medworm.com/index.php?rid=2887306&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19818829%26dopt%3DAbstract</link>
            <description>Authors: Wardenga R, Lindner HA, Hollmann F, Thum O, Bornscheuer U
    Aminoacylase-1 from pig kidney (pAcy1) catalyzes the highly stereoselective acylation of amino acids, a useful conversion for the preparation of optically pure N-acyl-l-amino acids. The kinetic of this thermodynamically controlled conversion is determined by maximal velocities for synthesis (V(mS)) and hydrolysis (V(mH)) of the N-acyl-l-amino acid. To investigate which parameter affects maximal velocities, we focused on the proton acceptor potential of the catalytic base, E146, and studied the influence of the active site architecture on its contribution to the pKa of residue E146. The modeled structure of pAcy1 identified residue D346 as having the strongest impact on the electrostatic features of the catalytic base. S...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2887306</comments>
            <pubDate>Wed, 07 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2887306</guid>        </item>
        <item>
            <title>Docosahexaenoic acid modulates the expression of T-bet and GATA-3 transcription factors, independently of PPARalpha, through suppression of MAP kinase activation.</title>
            <link>http://www.medworm.com/index.php?rid=2863228&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19799960%26dopt%3DAbstract</link>
            <description>Authors: Attakpa E, Hichami A, Simonin AM, Sans&amp;#xF3;n EG, Dramane KL, Khan NA
    The present study was conducted on CD4(+) T cells, isolated from wild type (WT) and PPARalpha(null) mice, in order to assess the mechanism of action of docosahexaenoic acid (DHA), an n-3 fatty acid, in the modulation of two transcription factors, i.e., T-bet and GATA-3, implicated in T-cell differentiation towards, respectively, T(H)1 and T(H)2 phenotype. The T-cells from PPARalpha(null) mice secreted higher IFN-gamma and lower IL-4 concentrations than WT T-cells. Furthermore, the deletion of PPARalpha gene in T-cells resulted in the upregulation of T-bet and downregulation of GATA-3 both at mRNA and protein levels. DHA exerted not only an inhibitory effect on T-cell proliferation, but also diminished IFN-ga...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863228</comments>
            <pubDate>Wed, 30 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2863228</guid>        </item>
        <item>
            <title>Sialic acid-binding dwarf elder four-chain lectin displays nucleic acid N-glycosidase activity.</title>
            <link>http://www.medworm.com/index.php?rid=2863226&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19799962%26dopt%3DAbstract</link>
            <description>Authors: Iglesias R, Citores L, Ferreras JM, P&amp;#xE9;rez Y, Jim&amp;#xE9;nez P, Gayoso MJ, Olsnes S, Tamburino R, Di Maro A, Parente A, Girb&amp;#xE9;s T
    Sialic acid-binding dwarf elder agglutinin (SEA) present only in rhizomes of the medicinal plant Sambucus ebulus L., was found to be a tetrameric glycoprotein consisting of two covalently-associated dimers of an enzymic A chain with rRNA N-glycosidase activity (EC 3.2.2.22) linked to a B chain with agglutinin properties. The lectin inhibited protein synthesis by a cell-free system and depurinated ribosomes. Cloning of the corresponding gene and molecular modeling of the deduced amino acid sequence demonstrated that SEA has a three-dimensional structure which resembles that reported for other two tetrameric type 2 RIPs from Sambucus (SNAI and S...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863226</comments>
            <pubDate>Wed, 30 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2863226</guid>        </item>
        <item>
            <title>The quaternary structure of pyruvate kinase type 1 from E. coli at low nanomolar concentrations.</title>
            <link>http://www.medworm.com/index.php?rid=2863224&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19800933%26dopt%3DAbstract</link>
            <description>Authors: Zhu T, Bailey MF, Angley LM, Cooper TF, Dobson RC
    Pyruvate kinase (PK) is the key control point of glycolysis-the biochemical pathway central to energy metabolism and the production of precursors used in biosynthesis. PK type 1 from Escherichia coli (Ec-PK1) is activated by both fructose-1,6-bisphosphate (FBP) and its substrate, phosphoenol pyruvate (PEP). To date, it has not been possible to determine whether the enzyme is tetrameric at the low concentrations (i.e. low nM range) used to study the steady state kinetics, or assess whether its allosteric effectors alter the oligomeric state of the enzyme at these concentrations. Employing the new technique of analytical ultracentrifugation with fluorescence detection we have, for the first time, shown that the K(D)(4-2) for Ec-P...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863224</comments>
            <pubDate>Wed, 30 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2863224</guid>        </item>
        <item>
            <title>Characterisation of n-glycans bound to IGFBP-3 in sera from healthy adults.</title>
            <link>http://www.medworm.com/index.php?rid=2863225&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19800385%26dopt%3DAbstract</link>
            <description>This study represents a ground for the future research of glycosylation pattern of IGFBP-3 from the circulation of men and women diagnosed with different illnesses.
    PMID: 19800385 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863225</comments>
            <pubDate>Tue, 29 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2863225</guid>        </item>
        <item>
            <title>Aldose-6-phosphate reductase from apple leaves:Importance of the quaternary structure for enzyme activity.</title>
            <link>http://www.medworm.com/index.php?rid=2863227&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19799961%26dopt%3DAbstract</link>
            <description>Authors: Figueroa CM, Iglesias AA
    Aldose-6-phosphate reductase (A6PRase) is a key enzyme for glucitol biosynthesis in plants from the Rosaceae family. To gain on molecular tools for enzymological studies, we developed an accurate system for the heterologous expression of A6PRase from apple leaves. The recombinant enzyme was expressed with a His-tag alternatively placed in the N-or C-terminus, thus allowing the one-step protein purification by immobilized metal affinity chromatography. Both, the N-and theC-term tagged enzymes exhibited similar affinity toward substrates, although thek(cat) of the latter enzyme was 80-fold lower than that having the His-tag in the N-term. Gel filtration chromatography showed different oligomeric structures arranged by the N-(dimer) and the C-term (monome...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863227</comments>
            <pubDate>Mon, 28 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2863227</guid>        </item>
        <item>
            <title>Molecular dynamics analysis of the wild type and dF508 mutant structures of the human CFTR-nucleotide binding domain 1.</title>
            <link>http://www.medworm.com/index.php?rid=2847149&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19781595%26dopt%3DAbstract</link>
            <description>Authors: Bisignano P, Moran O
    Mutations of CFTR (Cystic Fibrosis transmembrane Conductance Regulator), a membrane protein expressed in the epithelium, a chloride channel cause a chronic, developmental and hereditary disease, known as Cystic Fibrosis. The most common mutation is the deletion of F508, the residue present in the first nucleotide binding domain (NBD1). We studied the thermodynamic properties of NBD1 wild type (WT) and mutant (dF508), starting from the crystallographic structures in the Protein Data Bank using the techniques of Molecular Dynamics. The two structures were similarly stable at room temperature, showed no change enthalpy or entropy, maintaining the same dimensions and the same order of magnitude of atomic fluctuations; the only difference was the energy of inte...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2847149</comments>
            <pubDate>Wed, 23 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2847149</guid>        </item>
        <item>
            <title>Contraceptive steroids from pharmaceutical waste perturbate junctional communication in sertoli cells.</title>
            <link>http://www.medworm.com/index.php?rid=2834928&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19778577%26dopt%3DAbstract</link>
            <description>Authors: Tramoni M, Gilleron J, Tahiri K, Carette D, Corvol MT, Segretain D, Pointis G, Savouret JF
    The potential health impact of pharmaceutical waste is now a growing concern. Contraceptive steroids are prominent environmental contaminants and thus may act as endocrine disruptors. Numerous xenobiotics hamper Sertoli cells junctional communication which is known to participate in spermatogenesis control. This has been associated with male subfertility and testicular cancer. We investigated three contraceptive molecules found in the environment for their potential impact on Sertoli cells gap junction functionality: 17a-ethynylestradiol, medroxyprogesterone acetate and levonorgestrel. Four other non-steroid drugs also found in the environment were included in the study. Communication di...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2834928</comments>
            <pubDate>Sun, 20 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2834928</guid>        </item>
        <item>
            <title>Differential scanning calorimetric and spectroscopic studies on the unfolding of Momordica charantia lectin. Similar modes of thermal and chemical denaturation.</title>
            <link>http://www.medworm.com/index.php?rid=2834927&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19778578%26dopt%3DAbstract</link>
            <description>Authors: Kavitha M, Bobbili KB, Swamy MJ
    Thermal stability of Momordica charantia seed lectin (MCL) was investigated as a function of protein concentration, pH, scan rate, and at different ligand concentrations by using high-sensitivity differential scanning calorimetry (DSC). The DSC endotherm obtained at pH 7.4 consists of two entities with transition temperatures at ca. 333.7 K, and 338 K. The unfolding process is irreversible and could be described by a three-state model. For MCL tetramer DeltaH(c)/DeltaH(v) ratio is close to 4 for the first transition and approximately 2 for the second transition, suggesting that four and two cooperative units are involved in the first and second transitions, respectively. In the presence of lactose both transitions shifted to higher temperatures,...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2834927</comments>
            <pubDate>Sun, 20 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2834927</guid>        </item>
        <item>
            <title>Modulation of the hepatic fatty acid pool in peroxisomal 3-ketoacyl-CoA thiolase B-null mice exposed to the selective PPARalpha agonist Wy14,643.</title>
            <link>http://www.medworm.com/index.php?rid=2829129&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19772884%26dopt%3DAbstract</link>
            <description>Authors: Arnauld S, Fidaleo M, Cl&amp;#xE9;mencet MC, Chevillard G, Athias A, Gresti J, Wanders RJ, Latruffe N, Nicolas-Franc&amp;#xE8;s V, Mandard S
    The peroxisomal 3-ketoacyl-CoA thiolase B (Thb) gene was previously identified as a direct target gene of PPARalpha, a nuclear hormone receptor activated by hypolipidemic fibrate drugs. To better understand the role of ThB in hepatic lipid metabolism in mice, Sv129 wild-type and Thb null mice were fed or not the selective PPARalpha agonist Wy14,643 (Wy). Here, it is shown that in contrast to some other mouse models deficient for peroxisomal enzymes, the hepatic PPARalpha signalling cascade in Thb null mice was normal under regular conditions. It is of interest that the hypotriglyceridemic action of Wy was reduced in Thb null mice underlining the ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2829129</comments>
            <pubDate>Fri, 18 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2829129</guid>        </item>
        <item>
            <title>Structure and function of Plasmodium falciparum malate dehydrogenase: Role of critical amino acids in co-substrate binding pocket.</title>
            <link>http://www.medworm.com/index.php?rid=2829128&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19772885%26dopt%3DAbstract</link>
            <description>Authors: Pradhan A, Tripathi AK, Desai PV, Mukherjee PK, Avery MA, Walker LA, Tekwani BL
    The malaria parasite thrives on anaerobic fermentation of glucose for energy. Earlier studies from our laboratory have demonstrated that a cytosolic malate dehydrogenase (PfMDH) with striking similarity to lactate dehydrogenase (PfLDH) might complement PfLDH function in Plasmodium falciparum. The N-terminal glycine motif, which forms a characteristic Rossman dinucleotide-binding fold in the co-substrate binding pocket, differentiates PfMDH (GlyXGlyXXGly) from other eukaryotic and prokaryotic malate dehydrogenases (GlyXXGlyXXGly). The amino acids lining the co-substrate binding pocket are completely conserved in MDHs from different species of human, primate and rodent malaria parasites. Based on thi...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2829128</comments>
            <pubDate>Fri, 18 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2829128</guid>        </item>
        <item>
            <title>FAD binding in glycine oxidase from Bacillus subtilis.</title>
            <link>http://www.medworm.com/index.php?rid=2804794&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19751796%26dopt%3DAbstract</link>
            <description>Authors: Caldinelli L, Pedotti M, Motteran L, Molla G, Pollegioni L
    The apoprotein of the FAD-containing flavoenzyme glycine oxidase from Bacillus subtilis was obtained at pH 8.5 by dialyzing the holoenzyme against 2 M KBr in 0.25 M Tris-HCl and 20% glycerol. The apoprotein of glycine oxidase shows high protein fluorescence, high exposure of hydrophobic surfaces, and low temperature stability as compared to the holoenzyme. The isolated apoprotein species is present in solution as a monomer which rapidly recovers its tertiary structure and converts into the tetrameric holoenzyme following incubation with free FAD. The reconstitution process follows a particular two-stage process; the spectral properties of the reconstituted holoenzyme were virtually indistinguishable from those observed...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2804794</comments>
            <pubDate>Thu, 10 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2804794</guid>        </item>
        <item>
            <title>Nitrochalcones: Potential in vivo insulin secretagogues.</title>
            <link>http://www.medworm.com/index.php?rid=2797306&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19747522%26dopt%3DAbstract</link>
            <description>In this study, the in vivo and in vitro anti-hyperglycemic activity of chalcone derivatives of 3,4-methylenedioxy, with a substituent electron-acceptor nitro group in the A or B ring, was investigated. As expected, the second generation sulfonylurea glipizide stimulated insulin secretion and reduced glycemia over the study period. Also, it was demonstrated for the first time that chalcones are able to increase insulin secretion and this event was coincident with serum glucose-lowering in the oral glucose tolerance test. Additionally, the chalcones studied had a similar effect on insulin secretion and serum glucose-lowering as glipizide. The effect of chalcones in terms of inducing insulin secretion was greater than that of glipizide after 30 min. Moreover, chalcones were not able to stimul...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2797306</comments>
            <pubDate>Tue, 08 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2797306</guid>        </item>
        <item>
            <title>Phosphate facilitates Fe(II) oxidative deposition in pea seed (Pisum sativum) ferritin.</title>
            <link>http://www.medworm.com/index.php?rid=2782434&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19735693%26dopt%3DAbstract</link>
            <description>Authors: Li C, Qi X, Li M, Zhao G, Hu X
    The iron core within phytoferritin interior usually contains the high ratio of iron to phosphate, agreeing with the fact that phosphorus and iron are essential nutrient elements for plant growth. It was established that iron oxidation and incorporation into phytoferritin shell occurs in the plastid(s) where the high concentration of phosphate occurs. However, so far, the role of phosphate in iron oxidative deposition in plant ferritin has not been recognized yet. In the present study, Fe(II) oxidative deposition in pea seed ferritin (PSF) was aerobically investigated in the presence of phosphate. Results indicated that phosphate did not affect the stoichiometry of the initial iron(II) oxidation reaction that takes place at ferroxidase centers upo...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2782434</comments>
            <pubDate>Thu, 03 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2782434</guid>        </item>
        <item>
            <title>Identification of continuous interaction sites in PLA(2)-based protein complexes by peptide arrays.</title>
            <link>http://www.medworm.com/index.php?rid=2775150&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19733616%26dopt%3DAbstract</link>
            <description>Authors: Fortes-Dias CL, Santos RM, Magro AJ, Fontes MR, Ch&amp;#xE1;vez-Ol&amp;#xF3;rtegui C, Granier C
    Crotoxin (CA.CB) is a beta-neurotoxin from Crotalus durissus terrificus snake venom that is responsible for main envenomation effects upon biting by this snake. It is a heterodimer of an acidic protein (CA) devoid of any biological activity per se and a basic, enzymatically active, PLA(2) counterpart (CB). Both lethal and enzymatic activities of crotoxin have been shown to be inhibited by CNF, a protein from the blood of C. d. terrificus snakes. CNF replaces CA in the CA.CB complex, forming a stable, non-toxic complex CNF.CB. The molecular sites involved in the tight interfacial protein-protein interactions in these PLA(2)-based complexes have not been clearly determined, To help address th...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2775150</comments>
            <pubDate>Wed, 02 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2775150</guid>        </item>
        <item>
            <title>Natural compounds and the hypoxia-inducible factor (HIF) signalling pathway.</title>
            <link>http://www.medworm.com/index.php?rid=2735047&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19703512%26dopt%3DAbstract</link>
            <description>Authors: Manolescu B, Oprea E, Busu C, Cercasov C
    A decline in the tissue oxygen level below normal leads to cellular hypoxia. This situation is very frequently encountered in solid tumors as existing blood vessels cannot satisfy the requirements in oxygen of the rapidly growing tumor. Like hyperoxia, hypoxia is a stress factor for cells and tissues. Adapting to this stressful situation leads to activation of the dimeric transcription factor hypoxia-inducible factor-1 (HIF-1) that induces gene expression in promoting tumor cell survival. In addition, hypoxia acts as a selection factor for radio- and chemo-therapy resistant tumor cells with a high potential of malignancy. Consequently, over expression of the HIF-1alpha subunit is associated with an advanced disease stage and poor progno...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2735047</comments>
            <pubDate>Thu, 20 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2735047</guid>        </item>
        <item>
            <title>High aryl acylamidase activity associated with cobra venom acetylcholinesterase: Biological significance.</title>
            <link>http://www.medworm.com/index.php?rid=2723591&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19695303%26dopt%3DAbstract</link>
            <description>Authors: Rajesh RV, Layer PG, Boopathy R
    Investigation of the non-classical functions of cholinesterases (ChEs) has been the subject of interest in the past three decades. One of which is aryl acylamidase (AAA) activity associated with ChEs, but characterized in in vitro, as an enzyme, splitting the artificial substrate o-nitroacetanilide with unknown physiological function. In the present study, we have compared levels of AAA activity of AChE from different sources like goat brain, electric eel organ and from venoms of different snakes. Remarkably cobra venom showed the highest AAA activity and also high AAA/AChE ratio. Both serotonergenic and cholinergic inhibitors inhibited the cobra venom AAA activity in a concentration dependent manner, which also underlines the association of AAA...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2723591</comments>
            <pubDate>Sun, 16 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2723591</guid>        </item>
        <item>
            <title>The first alpha-1,3-glucosidase from bacterial origin belonging to glycoside hydrolase family 31.</title>
            <link>http://www.medworm.com/index.php?rid=2712900&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19683032%26dopt%3DAbstract</link>
            <description>Authors: Kang MS, Okuyama M, Mori H, Kimura A
    Genome analysis of Lactobacillus johnsonii NCC533 has been recently completed. One of its annotated genes, lj0569, encodes the protein having the conserved domain of glycoside hydrolase family 31. Its homolog gene (ljag31) in L. johnsonii NBRC13952 was cloned and expressed using an Escherichia coli expression system, resulting in poor production of recombinant LJAG31 protein due to inclusion body formation. Production of soluble recombinant LJAG31 was improved with high concentration of NaCl in medium, possible endogenous chaperone induction by benzyl alcohol, and over-expression of GroES-GroEL chaperones. Recombinant LJAG31 was an alpha-glucosidase with broad substrate specificity toward both homogeneous and heterogeneous substrates. This ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2712900</comments>
            <pubDate>Wed, 12 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2712900</guid>        </item>
        <item>
            <title>Revisiting Delta-6 Desaturase regulation by C18 unsaturated fatty acids, depending on the nutritional status.</title>
            <link>http://www.medworm.com/index.php?rid=2703035&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19679157%26dopt%3DAbstract</link>
            <description>Authors: Skrzypski J, Bellenger S, Bellenger J, Sinclair A, Poisson JP, Tessier C, Rialland M, Narce M
    Dietary polyunsaturated fatty acids (PUFA) play a key role in regulating delta-6 desaturase (D6D), the key enzyme for long chain PUFA biosynthesis. Nevertheless, the extent of their effects on this enzyme remains controversial and difficult to assess. It has been generally admitted that C18 unsaturated fatty acids (UFAs) regulate negatively delta-6 desaturase (D6D). This inhibition has been evidenced in regard to a high glucose/fat free (HG/FF) diet used in reference. However, several nutritional investigations did not evidence any inhibition of desaturases when feeding fatty acids. Because the choice of the basal diet appeared to be of primary importance in such experiments, our goal...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2703035</comments>
            <pubDate>Sun, 09 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2703035</guid>        </item>
        <item>
            <title>Dissimilarity in the channel intrinsic stability among the bacterial KcsA and the inwardly rectifying potassium channel ROMK1.</title>
            <link>http://www.medworm.com/index.php?rid=2703034&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19679158%26dopt%3DAbstract</link>
            <description>In this study, we compared the channel intrinsic stability of the bacterial K(+)-channel KcsA and the inwardly rectifying potassium channel (Kir) ROMK1. ROMK1 was successfully cloned, expressed and purified from Saccharomyces cerevisae. By conventional gel electrophoresis, ROMK1 was detected in monomeric form running exclusively at ~45 kDa either in its oxidized or reduced form. By perfluoro-octanoic acid (PFO)-PAGE, the reduced ROMK1 was identified as tetrameric as well as oligomeric complex. However, in its oxidized form ROMK1 was exclusively detected in oligomeric form thus indicating the role of intrinsic cysteine residues and formation of disulfide bonds in stabilizing the oligomeric ROMK1. On the other hand, KcsA purified from E. coli was detected as an extremely stable tetramer both...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2703034</comments>
            <pubDate>Sun, 09 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2703034</guid>        </item>
        <item>
            <title>Plasma fatty acid levels may regulate the Zn(2+)-dependent activities of histidine-rich glycoprotein.</title>
            <link>http://www.medworm.com/index.php?rid=2703033&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19679159%26dopt%3DAbstract</link>
            <description>Authors: Stewart AJ, Blindauer CA, Sadler PJ
    Histidine-rich glycoprotein (HRG) is a plasma adaptor protein involved in the formation of protein complexes that regulate a number of biological processes in the blood, most notably coagulation and the immune system. Elevated levels of HRG are clinically linked to thrombotic disorders such as blood vessel occlusion. A large body of evidence suggests that Zn(2+) ions stimulates HRG-complex formation; however, under normal conditions the vast majority of Zn(2+) in the blood is bound to human serum albumin (HSA). We have previously demonstrated that high levels of fatty acid act as an allosteric switch which disrupts the major Zn(2+)-binding site on HSA. Transient or sustained elevation of plasma fatty acid levels may therefore increase the pr...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2703033</comments>
            <pubDate>Sun, 09 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2703033</guid>        </item>
        <item>
            <title>Characterization of papain-like isoenzymes from latex of Asclepias curassavica by molecular biology validated by proteomic approach.</title>
            <link>http://www.medworm.com/index.php?rid=2703032&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19679160%26dopt%3DAbstract</link>
            <description>Authors: Obreg&amp;#xF3;n WD, Liggieri CS, Trejo SA, Avil&amp;#xE9;s FX, Vairo-Cavalli SE, Priolo NS
    Latices from Asclepias spp are used in wound healing and the treatment of some digestive disorders. These pharmacological actions have been attributed to the presence of cysteine proteases in these milky latices. Asclepias curassavica (Asclepiadaceae),&quot;scarlet milkweed &quot; is a perennial subshrub native to South America. In the current paper we report a new approach directed at the selective biochemical and molecular characterization of asclepain cI (acI) and asclepain cII (acII), the enzymes responsible for the proteolytic activity of the scarlet milkweed latex. SDS-PAGE spots of both purified peptidases were digested with trypsin and Peptide Mass Fingerprints (PMFs) obtained showed no equivalen...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2703032</comments>
            <pubDate>Sun, 09 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2703032</guid>        </item>
        <item>
            <title>Prediction of the protein folding core: application to the immunoglobulin fold.</title>
            <link>http://www.medworm.com/index.php?rid=2696699&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19665046%26dopt%3DAbstract</link>
            <description>Authors: Prudhomme N, Chomilier J
    We propose an algorithm that allows predicting residues important for the formation of the structure of globular proteins. It relies on a simulation that detects the amino acids presenting a maximum number of neighbours during the early steps of the folding process. They have been called MIR (Most Interacting Residues). Independently, description of the protein structures in fragments with closed ends shows the correlation between these extremities and the core of the globules. These fragments are of rather constant length, typically between 20 and 25 amino acids, and we have previously shown that their extremities are preferentially occupied by MIR. Introduction of rules derived from this fragment analysis of tertiary structures allows to smooth the d...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2696699</comments>
            <pubDate>Tue, 04 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2696699</guid>        </item>
        <item>
            <title>2'-phosphodiesterase and 2',5'-oligoadenylate synthetase activities in the lowest metazoans, sponge [porifera].</title>
            <link>http://www.medworm.com/index.php?rid=2696698&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19665065%26dopt%3DAbstract</link>
            <description>Authors: Saby E, Poulsen JB, Justesen J, Kelve M, Uriz MJ
    Sponges [porifera], the most ancient metazoans, contain modules related to the vertebrate immunity system, including the 2',5'-oligoadenylate synthetase (OAS). The components of the antiviral 2',5'-oligoadenylate (2-5A) system (OAS, 2'-Phosphodiesterase (2'-PDE) and RNAse L) of vertebrates have not all been identified in sponges. Here, we demonstrate for the first time that in addition to the OAS activity, sponges possess a 2'-PDE activity, which highlights the probable existence of a premature 2-5A system. Indeed, Suberites domuncula and Crella elegans exhibited this 2-5A degrading activity. Upon this finding, two out of three elements forming the 2-5A system have been found in sponges, only a endoribonuclease, RNAse L or simil...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2696698</comments>
            <pubDate>Tue, 04 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2696698</guid>        </item>
        <item>
            <title>The human large subunit ribosomal protein L36A-like contacts the CCA end of P-site bound tRNA.</title>
            <link>http://www.medworm.com/index.php?rid=2668373&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19647033%26dopt%3DAbstract</link>
            <description>Authors: Baouz S, Woisard A, Sinapah S, Le Caer JP, Argentini M, Bulygin K, Agui&amp;#xE9; G, Hountondji C
    Periodate-oxidized tRNA (tRNAox), the 2',3'-dialdehyde derivative of tRNA, was used as a zero-length active site-directed affinity labeling reagent, to covalently label proteins at the binding site for the 3'-end of tRNA on human 80S ribosomes. When human 80S ribosomes were reacted with tRNA(Asp)ox positioned at the P-site, in the presence of an appropriate 12 mer mRNA, a set of two tRNAox-labeled ribosomal proteins (rPs) was observed. The majorily labeled protein was identified as the large subunit rP L36a-like (RPL36AL) by means of mass spectrometry. Intact tRNA(Asp) competed with tRNA(Asp)ox for the binding to the P-site, by preventing tRNA-protein cross-linking with RPL36AL. Altog...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2668373</comments>
            <pubDate>Wed, 29 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2668373</guid>        </item>
        <item>
            <title>N-myristoylation targets dihydroceramide Delta4-desaturase 1 to mitochondria: Partial involvement in the apoptotic effect of myristic acid.</title>
            <link>http://www.medworm.com/index.php?rid=2668375&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19647031%26dopt%3DAbstract</link>
            <description>This study was designed to analyze the effect of myristic acid on ceramide synthesis and its related lipoapoptosis pathway. It was previously observed that myristic acid binds dihydroceramide Delta4-desaturase 1 (DES1) through N-myristoylation and activates this enzyme involved in the final de novo ceramide biosynthesis step. In the present study, we show first by immunofluorescence microscopy and subcellular fractionation that DES1 myristoylation targets part of the recombinant protein to the mitochondria in COS-7 cells. In addition, native dihydroceramide Delta4-desaturase activity was found in both the endoplasmic reticulum and mitochondria in rat hepatocytes. Dihydroceramide conversion to ceramide was increased in COS-7 cells expressing DES1 and incubated with myristic acid. The expres...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2668375</comments>
            <pubDate>Tue, 28 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2668375</guid>        </item>
        <item>
            <title>Wilson Disease: Current Status and the Future.</title>
            <link>http://www.medworm.com/index.php?rid=2668374&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19647032%26dopt%3DAbstract</link>
            <description>Authors: Schilsky ML
    The focus of this minireview is on the current status and new advances in diagnosis and treatment of Wilson disease, an autosomal recessive disorder of copper metabolism. Molecular diagnostics have improved and complements current biochemical and clinical methods for screening for Wilson disease. Screening for Wilson disease in newborns is feasible and has been tested in limited populations, but is not yet widely performed. Identification of patients with Wilson disease as the cause lof acute liver failure is possible using standard biochemical tests. Treatments for Wilson disease include chelating agents and zinc salts and liver transplantation. Future therapies may include hepatocyte transplantation and gene therapy, both of which have been tested and shown to wo...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2668374</comments>
            <pubDate>Tue, 28 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2668374</guid>        </item>
        <item>
            <title>Metals in health: From cell to soil, a multiscale approach.</title>
            <link>http://www.medworm.com/index.php?rid=2645828&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19631250%26dopt%3DAbstract</link>
            <description>Authors: Curis E, Nicolis I, B&amp;#xE9;nazeth S
    
    PMID: 19631250 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2645828</comments>
            <pubDate>Tue, 21 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2645828</guid>        </item>
        <item>
            <title>Enzymatic characterization of a monomeric isocitrate dehydrogenase from Streptomyces lividans TK54.</title>
            <link>http://www.medworm.com/index.php?rid=2645827&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19631711%26dopt%3DAbstract</link>
            <description>Authors: Zhang B, Wang B, Wang P, Cao Z, Huang E, Hao J, Dean AM, Zhu G
    Isocitrate dehydrogenase (IDH) is one of the key enzymes in the citric acid cycle, which involves in providing energy and biosynthetic precursors for metabolism. Here, we report for the first time the enzymatic characterization of a monomeric NADP(+)-dependent IDH from Streptomyces lividans TK54 (SlIDH). The icd gene (GenBank database accession number EU661252) encoding IDH was cloned and overexpressed in Escherichia coli. The molecular mass of SlIDH was about 80 kDa, typical of a monomeric NADP-IDH, and showed high amino acid sequence identity with known monomeric IDHs. The optimal activity of the 6His-tagged SlIDH was found at pH values 8.5 (Mn(2+)) and 9.0 (Mg(2+)), and the optimal temperature was around 46 degr...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2645827</comments>
            <pubDate>Tue, 21 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2645827</guid>        </item>
        <item>
            <title>Platelet derived growth factor BB is a ligand for dermatan sulfate chain(s) of small matrix proteoglycans from normal and fibrosis affected fascia.</title>
            <link>http://www.medworm.com/index.php?rid=2645826&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19631712%26dopt%3DAbstract</link>
            <description>We examined by the solid phase assay the growth factor binding to DS chains of small proteoglycans from various fasciae as well as to standard CSs. Before the assay a structural analysis of DSs and CSs was accomplished involving the evaluation of their epimerization and/or sulfation patterns. In addition, in vivo acceptors for PDGF-BB in fibrosis affected fascia were detected. PDGF-BB binding sites on DSs/CSs are located in long chain sections with the same type of hexuronate isomer however without any apparent preference to glucuronate or iduronate residues. Alternatively, the interaction seems to involve two shorter DS chain sections assembling disaccharides with the same type of hexuronate isomer which are separated by disaccharide(s) with another hexuronate one. Moreover, DS/CS affinit...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2645826</comments>
            <pubDate>Tue, 21 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2645826</guid>        </item>
        <item>
            <title>Are there three polynucleotide strands in the catalytic center of DNA polymerases?</title>
            <link>http://www.medworm.com/index.php?rid=2640088&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19628017%26dopt%3DAbstract</link>
            <description>Authors: Lestienne PP
    Mitochondrial DNA may undergo large-scale rearrangements, thus leading to diseases. The mechanisms of these rearrangements are still the matter of debates. Several lines of evidence indicate that breakpoints are characterized by direct repeats (DR), one of them being eliminated from the normal genome. Analysis of DR showed their skewed nucleotide content compatible with the formation of known triple helices. Here, I propose a novel mechanism involving the formation of triplex structures that result from the dissociation of the [synthesized repeat-DNA polymerase] complex. Upon binding to the homologous sequence, replication is initiated from the primer bound in a triple helix manner. This feature implies the initiation of replication on the double-stranded DNA from...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2640088</comments>
            <pubDate>Sun, 19 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2640088</guid>        </item>
        <item>
            <title>Metallomics integrated with proteomics in deciphering metal-related environmental issues.</title>
            <link>http://www.medworm.com/index.php?rid=2627224&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19616599%26dopt%3DAbstract</link>
            <description>Authors: Gonz&amp;#xE1;lez-Fern&amp;#xE1;ndez M, Garc&amp;#xED;a-Barrera T, Jurado J, Pueyo C, L&amp;#xF3;pez-Barea J, G&amp;#xF3;mez-Ariza JL
    The present work shows the possibilities of metallomics to characterize metal-linking proteins in Mus Musculus that could be used in environmental assessment. The laboratory mouse M. musculus is used as reference of gene/protein sequence databases to address methodological approaches based on changes in transcripts regulation, proteins expression and metalloproteins profiles in the environmental bioindicator Mus spretus that has been demonstrated to be genetically homologous to M. Musculus. A metallomic approach using size exclusion chromatography with inductively coupled plasma-mass spectrometry detection (SEC-ICP-MS) was applied to cytosolic extracts from differe...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2627224</comments>
            <pubDate>Fri, 17 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2627224</guid>        </item>
        <item>
            <title>Peptide Derived from the Lipid Binding Domain of Group IB Human Pancreatic Phospholipase A(2) Possesses Antibacterial Activity.</title>
            <link>http://www.medworm.com/index.php?rid=2627223&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19619604%26dopt%3DAbstract</link>
            <description>In this study we report the antibacterial properties of a peptide (AVWQFRKMIK-CONH(2); N10 peptide), which corresponds to the N-terminal first ten amino acid residues of hp-sPLA(2), against E.coli. Full-length hp-sPLA(2), which contains this peptide sequence as N-terminal alpha-helix, did not showed detectable antibacterial activity. Presence of physiological concentration of salt or preincubation of N10 peptide with soluble anionic polymer inhibits the antibacterial activity indicating the importance of electrostatic interaction in binding of peptide to bacterial membrane. Addition of peptide resulted in destabilization of outer as well as inner cytoplasmic membrane of E. coli suggesting bacterial membranes to be the main target of action. N10 peptide exhibits strong synergism with lysozy...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2627223</comments>
            <pubDate>Thu, 16 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2627223</guid>        </item>
        <item>
            <title>EXAFS structural study of platinum-based anticancer drugs degradation in presence of sulfur nucleophilic species.</title>
            <link>http://www.medworm.com/index.php?rid=2614683&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19607872%26dopt%3DAbstract</link>
            <description>We present the main structural results we have obtained concerning the reaction of these drugs with diverse sulfur nucleophiles (cysteine, glutathione, methionine, thiosulfate and thiocyanate), monitored in solution or as precipitates by EXAFS spectroscopy. The reactivities of the carboxylate and amine ligands of both carboplatin and oxaliplatin are compared, on the basis of first coordination sphere modeling. Among the new results of this EXAFS study, we present the first observation of oxaliplatin diaminocyclohexane ligand displacement by sulfur nucleophiles.
    PMID: 19607872 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2614683</comments>
            <pubDate>Sun, 12 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2614683</guid>        </item>
        <item>
            <title>The aryl acylamidase activity is much more sensitive to Alzheimer drugs than the esterase activity of acetylcholinesterase in chicken embryonic brain.</title>
            <link>http://www.medworm.com/index.php?rid=2614682&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19607873%26dopt%3DAbstract</link>
            <description>In this study, an attempt has been made in profiling esterase and AAA activities of AChE at different developmental stages of the chick embryo, e.g. at embryonic day 6 (E6), E9, E12, E15 and E18. AAA activity showed a correlated expression with esterase activity at all stages, but the relative ratios of AAA to esterase activity were higher at younger stages. The inhibition of AAA activity was shown to be more sensitive towards Huperzine, Donepezil whereas inhibition of esterase activity was sensitive to Tacrine and DFP. Remarkably, the major Alzheimer drugs- Huperzine and Donepezil, much more strongly inhibited AAA activity of AChE at younger developmental stages whose IC50 values are 0.01muM and 0.1 muM respectively. In the case of BW284c51, inhibition was more pronounced at older stages ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2614682</comments>
            <pubDate>Fri, 10 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2614682</guid>        </item>
        <item>
            <title>c-Myc Mediates a Hypoxia-InducedDecrease in Acetylated Histone H4.</title>
            <link>http://www.medworm.com/index.php?rid=2602694&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19596041%26dopt%3DAbstract</link>
            <description>In this study, hypoxia (1% Oxygen) induced a decrease in both global acetylated histone H4 (AcH4) and c-Myc in human lung carcinoma A549 cells and in human bronchial epithelial Beas-2B cells, The decline was more stiking in A549 cells compared to Beas2-B cells, when cells were exposed to hypoxic stress for 24 hr. Further studies showed that these alterations of global AcH4 can be attributed to the decrease in c-Myc protein levels. While hypoxia-induced gene activation is known to be mediated by Hypoxia Response Elements (HRE), the mechanism for down-regulation of genes by hypoxia is not known. The decrease in c-Myc protein levels induced by hypoxia may contribute to hypoxia-induced gene repression.
    PMID: 19596041 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2602694</comments>
            <pubDate>Thu, 09 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2602694</guid>        </item>
        <item>
            <title>Molecular identification of omega-amidase, the enzyme that is functionally coupled with glutamine transaminases, as the putative tumor suppressor Nit2.</title>
            <link>http://www.medworm.com/index.php?rid=2602693&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19596042%26dopt%3DAbstract</link>
            <description>Authors: Jaisson S, Veiga-Da-Cunha M, Van Schaftingen E
    Our purpose was to identify the sequence of omega-amidase, which hydrolyses the amide group of alpha-ketoglutaramate, a product formed by glutamine transaminases. In the Bacillus subtilis genome, the gene encoding a glutamine transaminase (mtnV) is flanked by a gene encoding a putative 'carbon-nitrogen hydrolase'. The closest mammalian homolog of this putative bacterial omega-amidase is 'nitrilase 2', whose size and amino acid composition were in good agreement with those reported for purified rat liver omega-amidase. Mouse nitrilase 2 was expressed in Escherichia coli, purified and shown to catalyse the hydrolysis of alpha-ketoglutaramate and other known substrates of omega-amidase. No such activity was observed with mouse nitril...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2602693</comments>
            <pubDate>Thu, 09 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2602693</guid>        </item>
        <item>
            <title>Identification of the putative tumor suppressor Nit2 as omega-amidase, an enzyme metabolically linked to glutamine and asparagine transamination.</title>
            <link>http://www.medworm.com/index.php?rid=2602695&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19595734%26dopt%3DAbstract</link>
            <description>Authors: Krasnikov BF, Chien CH, Nostramo R, Pinto JT, Nieves E, Callaway M, Sun J, Huebner K, Cooper AJ
    The present report identifies the enzymatic substrates of a member of the mammalian nitrilase-like (Nit) family. Nit2, which is widely distributed in nature, has been suggested to be a tumor suppressor protein. The protein was assumed to be an amidase based on sequence homology to other amidases and on the presence of a putative amidase-like active site. This assumption was recently confirmed by the publication of the crystal structure of mouse Nit2. However, the in vivo substrates were not previously identified. Here we report that rat liver Nit2 is omega-amidodicarboxylate amidohydrolase (E.C. 3.5.1.3; abbreviated omega-amidase), a ubiquitously expressed enzyme that catalyzes a va...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2602695</comments>
            <pubDate>Wed, 08 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2602695</guid>        </item>
        <item>
            <title>Mathematical Modeling in Metal Metabolism: Overview and Perspectives.</title>
            <link>http://www.medworm.com/index.php?rid=2602692&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19596399%26dopt%3DAbstract</link>
            <description>Authors: Curis E, Nicolis I, Bensaci J, Deschamps P, B&amp;#xE9;nazeth S
    A review of mathematical modeling in metal metabolism is presented. Both endogenous and exogenous metals are considered. Four classes of methods are considered: Petri nets, multi-agent systems, determinist models based on differential equations and stochastic models. For each, a basic theoretical background is given, then examples of applications are given, detailed and commented. Advantages and disadvantages of each class of model are presented. A special attention is given to determinist differential equation models, since almost all models belong to this class.
    PMID: 19596399 [PubMed - as supplied by publisher] (Source: Biochimie)</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2602692</comments>
            <pubDate>Tue, 07 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2602692</guid>        </item>
        <item>
            <title>HIV-1 integrase-hydrolyzing antibodies from sera of HIV-infected patients.</title>
            <link>http://www.medworm.com/index.php?rid=2585311&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19580842%26dopt%3DAbstract</link>
            <description>We present evidence showing that 89.5 % IgGs purified from the sera of HIV-infected patients using several affinity resins including Sepharose with immobilized integrase specifically hydrolyze only HIV integrase (IN) but not many other tested proteins. Several rigid criteria have been applied to show that the IN-hydrolyzing activity is an intrinsic property of AIDS IgGs but not from healthy donors. Similar to autoimmune proteolytic abzymes, IN-hydrolyzing IgGs from some patients were inhibited by specific inhibitors of serine and metal-dependent proteases but a significant inhibition of the activity by specific inhibitors of acidic- and thiol-like proteases was observed for the first time. Although HIV-infection leads to formation of Abs to many viral and human antigens, no possible biolog...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2585311</comments>
            <pubDate>Thu, 02 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2585311</guid>        </item>
        <item>
            <title>Biochemical characterisation of the D60A mutant of the elongation factor 1alpha from the archaeon Sulfolobus solfataricus.</title>
            <link>http://www.medworm.com/index.php?rid=2547527&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19375481%26dopt%3DAbstract</link>
            <description>Authors: Ruggiero I, Cantiello P, Lamberti A, Sorrentino A, Martucci NM, Ruggiero A, Arcone R, Vitagliano L, Arcari P, Masullo M
    The D60A mutant of the elongation factor (EF) 1alpha from Sulfolobus solfataricus (Ss), was obtained as heterologous expressed protein and characterised. This substitution was carried out in order to analyse the involvement of this evolutionally conserved amino acid position in the interaction between the elongation factor and guanosine nucleotides and in the coordination of magnesium ions. The expression system used produced a folded protein able to catalyse, although to a slightly lower extent with respect to the wild-type enzyme, protein synthesis in vitro and NaCl-dependent intrinsic GTPase activity. The affinity for guanosine nucleotides was almost ident...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547527</comments>
            <pubDate>Sun, 28 Jun 2009 04:30:18 +0100</pubDate>
            <guid isPermaLink="false">2547527</guid>        </item>
        <item>
            <title>Application of multivariate curve resolution-alternating least squares (MCR-ALS) for secondary structure resolving of proteins.</title>
            <link>http://www.medworm.com/index.php?rid=2547521&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19376189%26dopt%3DAbstract</link>
            <description>Authors: Shariati-Rad M, Hasani M
    Fourier transform infrared (FTIR) spectroscopy is the most common spectroscopic technique used for study of protein structure. Initially, band deconvolution techniques were applied to determine the secondary structure of proteins. Recently, several multivariate regression methods have been used to predict the secondary structure of proteins as an alternative to the previous methods. Multivariate curve resolution-alternating least squares (MCR-ALS) was applied on the FTIR spectra of proteins to resolve the fraction and spectral profiles of different structural motifs. Initial estimates of spectral profiles of different protein motifs were built using orthogonal projection approach (OPA). Predicted fractions of alpha-helix and beta-sheet obtained by MCR-...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547521</comments>
            <pubDate>Sun, 28 Jun 2009 04:30:09 +0100</pubDate>
            <guid isPermaLink="false">2547521</guid>        </item>
        <item>
            <title>Fine tuning gene expression through short DNA-protein binding cycles.</title>
            <link>http://www.medworm.com/index.php?rid=2547519&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19376190%26dopt%3DAbstract</link>
            <description>Authors: Michel D
    Certain transcription factors have recently been shown to interact with DNA in living cells, through very short binding cycles, contrasting with the data previously obtained in vitro, and with the view of a stepwise building of transcription initiation complexes. These short cycles are triggered by active dissociation mechanisms, suggesting that they ensure important biological functions. Various interpretations of these observations have been proposed, including a mechanism allowing the cell to switch off gene expression after removal of the inducer, or increasing the availability of free transcription factors. The interpretation examined here is that the brevity of the transcription factor turnovers favors the determinism of gene expression. For the genes with open ...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547519</comments>
            <pubDate>Sun, 28 Jun 2009 04:30:07 +0100</pubDate>
            <guid isPermaLink="false">2547519</guid>        </item>
        <item>
            <title>Signaling pathways of kaempferol-3-neohesperidoside in glycogen synthesis in rat soleus muscle.</title>
            <link>http://www.medworm.com/index.php?rid=2547517&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19376191%26dopt%3DAbstract</link>
            <description>Authors: Cazarolli LH, Folador P, Pizzolatti MG, Mena Barreto Silva FR
    Kaempferol 3-neohesperidoside is one of the several compounds that have been reported to have insulin-like properties in terms of glucose lowering. We studied the effect of kaempferol 3-neohesperidoside in glycogen synthesis in rat soleus muscle through the incorporation of (14)C-d-glucose in glycogen. Kaempferol 3-neohesperidoside stimulates glycogen synthesis in rat soleus muscle by approximately 2.38-fold. Insulin at 100 nM showed a stimulatory effect on glycogen synthesis when compared with the control group. The stimulatory effect of kaempferol 3-neophesperidoside on glycogen synthesis was inhibited by wortmannin, the phosphatidylinositol 3-kinase (PI3K) inhibitor, and enhanced by lithium chloride, a glycogen s...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547517</comments>
            <pubDate>Sun, 28 Jun 2009 04:30:04 +0100</pubDate>
            <guid isPermaLink="false">2547517</guid>        </item>
        <item>
            <title>Organization and dynamics of tryptophan residues in tetrameric and monomeric soybean agglutinin: studies by steady-state and time-resolved fluorescence, phosphorescence and chemical modification.</title>
            <link>http://www.medworm.com/index.php?rid=2547515&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19383525%26dopt%3DAbstract</link>
            <description>Authors: Molla AR, Maity SS, Ghosh S, Mandal DK
    We have investigated the organization and dynamics of tryptophan residues in tetrameric, monomeric and unfolded states of soybean agglutinin (SBA) by selective chemical modification, steady-state and time-resolved fluorescence, and phosphorescence. Oxidation with N-bromosuccinimide (NBS) modifies two tryptophans (Trp 60 and Trp 132) in tetramer, four (Trp 8, Trp 203 and previous two) in monomer, and all six (Trp 8, Trp 60, Trp 132, Trp 154, Trp 203 and Trp 226) in unfolded state. Utilizing wavelength-selective fluorescence approach, we have observed a red-edge excitation shift (REES) of 10 and 5 nm for tetramer and monomer, respectively. A more pronounced REES (21 nm) is observed after NBS oxidation. These results are supported by fluores...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547515</comments>
            <pubDate>Sun, 28 Jun 2009 04:30:02 +0100</pubDate>
            <guid isPermaLink="false">2547515</guid>        </item>
        <item>
            <title>Analysis of protein contacts into Protein Units.</title>
            <link>http://www.medworm.com/index.php?rid=2547513&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19383526%26dopt%3DAbstract</link>
            <description>Authors: Faure G, Bornot A, de Brevern AG
    Three-dimensional structures of proteins are the support of their biological functions. Their folds are maintained by inter-residue interactions which are one of the main focuses to understand the mechanisms of protein folding and stability. Furthermore, protein structures can be composed of single or multiple functional domains that can fold and function independently. Hence, dividing a protein into domains is useful for obtaining an accurate structure and function determination. In previous studies, we enlightened protein contact properties according to different definitions and developed a novel methodology named Protein Peeling. Within protein structures, Protein Peeling characterizes small successive compact units along the sequence called...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547513</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:59 +0100</pubDate>
            <guid isPermaLink="false">2547513</guid>        </item>
        <item>
            <title>Moonlighting protein in Starkeyomyces koorchalomoides: characterization of dihydrolipoamide dehydrogenase as a protein acetyltransferase utilizing acetoxycoumarin as the acetyl group donor.</title>
            <link>http://www.medworm.com/index.php?rid=2547511&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19383527%26dopt%3DAbstract</link>
            <description>In this report we have identified for the first time a transacetylase (TAase) in a mesophilic fungi Starkeyomyces koorchalomoides catalyzing the transfer of acetyl group from polyphenolic acetate (PA) to a receptor protein glutathione S-transferase (GST). An elegant assay procedure was established for TAase based on its ability to mediate inhibition of GST by 7,8-diacetoxy-4-methylcoumarin (DAMC), a model PA. Utilizing this assay procedure, S. koorchalomoides TAase was purified to homogeneity. TAase was found to have MW of 50 kDa. The purified enzyme exhibited maximum activity at 45 degrees C at pH 6.8. The N-terminal sequence of purified fungal TAase (ANDASTVED) showed identity with corresponding N-terminal sequence of dihydrolipoamide dehydrogenase (LADH), a mitochondrial matrix enzyme a...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547511</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:57 +0100</pubDate>
            <guid isPermaLink="false">2547511</guid>        </item>
        <item>
            <title>Expression, purification, and characterization of the intra-cellular domain of the ANP receptor.</title>
            <link>http://www.medworm.com/index.php?rid=2547507&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19393286%26dopt%3DAbstract</link>
            <description>We report here the baculovirus expression and purification of the GCA intra-cellular domain construct GCA(ID) comprising the complete intra-cellular region which includes the kinase-homology domain, coiled-coil region, and catalytic cyclase domain. The intra-cellular domain was enzymatically characterized in terms of guanylyl cyclase activity and the effects of ATP, manganese, and Triton X-100. Our results indicate that the activity of the intra-cellular domain of the ANP receptor is about 2 fold less active compared to a truncated cyclase domain construct lacking the kinase-like domain that was also expressed and purified. In addition, unlike the full length receptor, the intra-cellular domain could not be activated by Triton X-100/Mn(2+) or its activity stimulated by ATP. These data ther...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547507</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:52 +0100</pubDate>
            <guid isPermaLink="false">2547507</guid>        </item>
        <item>
            <title>Targeting the G-quadruplex-forming region near the P1 promoter in the human BCL-2 gene with the cationic porphyrin TMPyP4 and with the complementary C-rich strand.</title>
            <link>http://www.medworm.com/index.php?rid=2547503&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19401211%26dopt%3DAbstract</link>
            <description>Authors: Del Toro M, Bucek P, Avi&amp;#xF1;&amp;#xF3; A, Jaumot J, Gonz&amp;#xE1;lez C, Eritja R, Gargallo R
    The B-cell lymphoma-2 (bcl-2) gene contains a region that has been implicated in the regulation of bcl-2 gene expression. This region can form G-quadruplex structures in solution [J.X. Dai, T.S. Dexheimer, D. Chen, M. Carver, A. Ambrus, R.A. Jones, D.Z. Yang, An intramolecular G-quadruplex structure with mixed parallel/antiparallel G-strands formed in the human BCL-2 promoter region in solution, J. Am. Chem. Soc. 128 (2006) 1096-1098.]. Here, we examined the acid-base and conformational equilibria of this G-quadruplex-forming region (BCL2G), as well as its interaction with both the porphyrin TMPyP4 and with the complementary C-rich strand. We used molecular absorption and circular dichroism...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547503</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:47 +0100</pubDate>
            <guid isPermaLink="false">2547503</guid>        </item>
        <item>
            <title>Mapping of 5' and 3'-ends of sunflower mitochondrial nad6 mRNAs reveals a very complex transcription pattern which includes primary transcripts lacking 5'-UTR.</title>
            <link>http://www.medworm.com/index.php?rid=2547501&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19401212%26dopt%3DAbstract</link>
            <description>Authors: Placido A, Regina TM, Quagliariello C, Volpicella M, Gallerani R, Ceci LR
    Nad6 orf, encoded in the sunflower mitochondrial genome in single copy contains a non-conserved 3'-extension. The transcription of the nad6 locus generates a highly complex pattern. Three main transcripts of 1240, 960 and 870 nt have been characterized by different approaches. The two smaller ones are apparently the most abundant of the steady-state RNA population and are generated as primary transcription products as well as by processing of the 1240 nt transcript. Their 5'-UTRs are absent or very short. Whereas the 3'-ends of the 960 nt transcripts contain a TGA codon the shorter one terminates at positions excluding the stop codon. The fate of transcripts to promote the synthesis of NAD6 sunflower pro...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547501</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:44 +0100</pubDate>
            <guid isPermaLink="false">2547501</guid>        </item>
        <item>
            <title>Identification by high throughput screening of small compounds inhibiting the nucleic acid destabilization activity of the HIV-1 nucleocapsid protein.</title>
            <link>http://www.medworm.com/index.php?rid=2547499&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19401213%26dopt%3DAbstract</link>
            <description>Authors: Shvadchak V, Sanglier S, Rocle S, Villa P, Haiech J, Hibert M, Van Dorsselaer A, M&amp;#xE9;ly Y, de Rocquigny H
    Due to its highly conserved zinc fingers and its nucleic acid chaperone properties which are critical for HIV-1 replication, the nucleocapsid protein (NC) constitutes a major target in AIDS therapy. Different families of molecules targeting NC zinc fingers and/or inhibiting the binding of NC with its target nucleic acids have been developed. However, their limited specificity and their cellular toxicity prompted us to develop a screening assay to target molecules able to inhibit NC chaperone properties, and more specifically the initial NC-promoted destabilization of the nucleic acid secondary structure. Since this destabilization is critically dependent on the properly...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547499</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:42 +0100</pubDate>
            <guid isPermaLink="false">2547499</guid>        </item>
        <item>
            <title>Green fluorescent protein - Tagged HCV non-enveloped capsid like particles: development of a new tool for tracking HCV core uptake.</title>
            <link>http://www.medworm.com/index.php?rid=2547497&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19401214%26dopt%3DAbstract</link>
            <description>Authors: Katsarou K, Serti E, Tsitoura P, Lavdas AA, Varaklioti A, Pickl-Herk AM, Blaas D, Oz-Arslan D, Zhu R, Hinterdorfer P, Mavromara P, Georgopoulou U
    Circulating 'free' non-enveloped Hepatitis C virus (HCV) core protein has been demonstrated in HCV-infected patients, and HCV subgenomes with deletions of the envelope proteins have been previously identified. Initial studies from our laboratory, previously published, indicated that expression of HCV core in insect cells can direct the formation of capsid-like particles lacking the envelope glycoproteins. These protein nanospheres, morphologically similar to natural capsids, were shown to be taken up by human hepatic cells and to produce cell-signalling events. To follow the intracellular fate of these particles we fused the core pro...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547497</comments>
            <pubDate>Sun, 28 Jun 2009 04:29:39 +0100</pubDate>
            <guid isPermaLink="false">2547497</guid>        </item>
        <item>
            <title>Meeting Report: Second International Meeting on Quadruplex DNA.</title>
            <link>http://www.medworm.com/index.php?rid=2547437&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19555734%26dopt%3DAbstract</link>
            <description>Authors: Herbert BS, Huppert JL, Bradjohnson F, Lane AN, Phan AT
    A two and a half day meeting on G-quadruplexes was held in Louisville, KY, USA (April 18-21, 2009). A specific goal of this conference was to promote discussion on the biology of G-quadruplexes. In practice this was represented in four main ways, namely in biophysics, bio/nanotechnology, therapeutics, and what might be termed &quot;intrinsic biology&quot;. Research into the basic biophysical and structural properties of G-quadruplexes continues to be important for understanding biology, and for optimizing aptamers for therapeutic and bio/technological purposes. The meeting comprised two Keynote lectures, twenty-three invited talks, and forty-two posters covering various aspects of these topics using a wide variety of technologies.
...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547437</comments>
            <pubDate>Sun, 21 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2547437</guid>        </item>
        <item>
            <title>Hepcidin, master of the martial arts.</title>
            <link>http://www.medworm.com/index.php?rid=2547435&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19555735%26dopt%3DAbstract</link>
            <description>Authors: Viatte L, Vaulont S
    Hepcidin, a peptide hormone produced by the liver, constitutes the master regulator of iron homeostasis in mammals allowing iron adaptation according to the body iron needs. In recent years there has been important breakthrough in our knowledge of hepcidin regulation that has also implications for understanding the physiopathology of human iron disorders. Different aspects of hepcidin regulation will be considered in this review, including regulation by the iron status and the BMP6/HJV/SMAD pathway. Hepcidin dysregulation in iron disorders will be also discussed. Although much can already be accomplished for treating iron disorders using the knowledge that has currently been developed, additional issues will be challenging for the coming years.
    PMID: 19...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547435</comments>
            <pubDate>Sun, 21 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2547435</guid>        </item>
        <item>
            <title>Phosphorylation of Bcl-2 and activation of caspase-3 via the c-Jun N-terminal kinase pathway in ursolic acid-induced DU145 cells apoptosis.</title>
            <link>http://www.medworm.com/index.php?rid=2547439&amp;cid=s_34544_60_f&amp;fid=34544&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19545597%26dopt%3DAbstract</link>
            <description>Authors: Zhang YX, Kong CZ, Wang HQ, Wang LH, Xu CL, Sun YH
    There is currently no successful therapy for androgen-independent prostate cancer. Ursolic acid (UA), a pentacyclic triterpenoid compound, has been shown to have an anti-proliferative effect on various tumors. We investigated the effect of UA on cell viability in the human hormone-refractory prostate cancer cell line DU-145, as well as the molecular mechanisms underlying its growth inhibiting effect. We demonstrated that UA induces apoptosis and the activation of caspase-3 in DU145 cells. UA also causes the activation of c-Jun N-terminal kinase (JNK), but has no effect on extracellular signal-regulated protein kinases (ERK1/2) and p38 MAP kinases (p38). UA-induced JNK activation could result in Bcl-2 phosphorylation (Ser70) an...</description>
            <author>Biochimie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2547439</comments>
            <pubDate>Thu, 18 Jun 2009 23:00:00 +0100</pubDate>
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