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<title><![CDATA[Progress in Biochemistry and Biophysics -->Next Issue Table of Contents]]></title>
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<title><![CDATA[Proteomic analysis of biofilm related proteins in RP62A]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20070404]]></link>
<description><![CDATA[Proteomics has been increasingly used as tools to analyze bacteria. S. epidermidis ATCC35984 (RP62A), a biofilm-positive strain, can cause subacute or chronic human skin infections which are difficult to cure. In this study, a combined strategy including 2DE-MS, shotgun-LC-MS and 1DE-LC-MS approaches was used to investigate proteins related to the biofilm formation. 82 proteins associated closely with pathogenesis and biofilm formation were identified with the combined strategy. At the same time, 164 specific hypothetical proteins which may catalyze unique functions in RP62A were verified. All these proteomic findings could help to deeply understand this bacterium and the disease associated with it.]]></description>
<pubDate>2008/2/3 0:00:00</pubDate>
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<author><![CDATA[Li Na,yangxiaomei,caoxingjun,caozhiwei,weiwu,xuhao,xiuqingping,jiangjuan,jinhong,zengrong,qudi and yangpengyuan]]></author>
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<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20250038_]]></link>
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<title><![CDATA[DCVs Exocytosis is Damaged in The Dominant Allele of β-G Spectrin Mutant in <i>C. elegans</i>]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20090365]]></link>
<description><![CDATA[β-Spectrin is a major component of the membrane skeleton, a structure found at the plasma membrane of most animal cells. <i>C. elegans</i> genome encodes only one gene of β-spectrin subunit (β-G), <i>unc-70</i>. Besides stabilizing plasma membranes and generating cell polarity, β-spectrin is also reported to mediate the secretary pathway. In the present studies, it was demonstrated that UNC-70 is involved in the dense core vesicle (DCV) exocytosis in <i>C. elegans</i> neurons. It was found that <i>unc-70</i> dominant allele mutants exhibited reduced peptide release <i>in vivo</i>. In IDA-1 (related to islet cell diabetes autoantigen) labeled ALA neurons, which serve as a good model for studying DCV exocytosis, mutant of β-spectrin leads to visible reduction of the readily released pool (RRP) size. The analysis of vesicular docking by total internal reflection microscopy revealed that loss-of-function of <i>unc-70</i> hindered the docking of DCVs in neurons. The electrophysiological experiments at the neuromuscular junctions excluded the possibility that the quantum size of acetylcholine in synaptic vesicles in neurous and postsynaptic response in muscle cells were affected. The above results provide evidences that  β-spectrin is required for the exocytosis of DCVs and also possibly involved in the release of neurotransmitter.]]></description>
<pubDate>2009/9/16 0:00:00</pubDate>
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<author><![CDATA[JIU Ya-Ming,YU Jun-Wei,LIN Xian-Guang,ZHANG Yong-Deng,WANG Yan,ZHANG Rong-Ying and WU Zheng-Xing]]></author>
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