Literature DB >> 16315178

Two-dimensional gel electrophoresis maps of the proteome and phosphoproteome of primitively cultured rat mesangial cells.

Xiao-Sheng Jiang1, Liu-Ya Tang, Xing-Jun Cao, Hu Zhou, Qi-Chang Xia, Jia-Rui Wu, Rong Zeng.   

Abstract

Mesangial cells (MC) play an important role in maintaining the structure and function of the glomerulus. The proliferation of MC is a prominent feature of many kinds of glomerular disease. The first reference 2-DE maps of rat mesangial cells (RMC), stained with silver staining or Pro-Q Diamond dye, have been established here to describe the proteome and phosphoproteome of RMC, respectively. A total of 157 selected protein spots, corresponding to 118 unique proteins, have been identified by MALDI-TOF-MS or LC-ESI-IT-MS/MS, in which 37 protein spots representing 28 unique proteins have also been stained with Pro-Q Diamond, indicating that they are in phosphorylated forms. All the identified proteins were bioinformatically annotated in detail according to their physiochemical characteristics, subcellular location, and function. Most of the separated or identified protein spots are distributed in the area of mass 10-70 kDa and pI 5.0-8.0. The identified proteins include mainly cytoplasmic and nuclear proteins and some mitochondrial, endoplasmic reticulum, and membrane proteins. These proteins are classified into different functional groups such as structure and mobility proteins (21.2%), metabolic enzymes (16.9%), protein folding and metabolism proteins (13.6%), signaling proteins (14.4%), heat-shock proteins (7.6%), and other functional proteins (12.7%). While structure and mobility proteins are mostly represented by protein spots with high abundance, signaling proteins are mostly represented by protein spots with relatively low abundance. Such a 2-DE database for RMC, especially with many signaling proteins and phosphoproteins characterized, will provide a valuable resource for comparative proteomics analysis of normal and pathologic conditions affecting MC function or pathologic progress.

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Year:  2005        PMID: 16315178     DOI: 10.1002/elps.200500286

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  10 in total

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Review 2.  Methods and approaches for the comprehensive characterization and quantification of cellular proteomes using mass spectrometry.

Authors:  Shama P Mirza; Michael Olivier
Journal:  Physiol Genomics       Date:  2007-12-27       Impact factor: 3.107

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4.  The anti-cancer activity of dihydroartemisinin is associated with induction of iron-dependent endoplasmic reticulum stress in colorectal carcinoma HCT116 cells.

Authors:  Jin-Jian Lu; Si-Meng Chen; Xiao-Wei Zhang; Jian Ding; Ling-Hua Meng
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5.  Quantitative proteomics analysis of inborn errors of cholesterol synthesis: identification of altered metabolic pathways in DHCR7 and SC5D deficiency.

Authors:  Xiao-Sheng Jiang; Peter S Backlund; Christopher A Wassif; Alfred L Yergey; Forbes D Porter
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6.  Activation of Rho GTPases in Smith-Lemli-Opitz syndrome: pathophysiological and clinical implications.

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7.  Quantitative proteomic analysis of Niemann-Pick disease, type C1 cerebellum identifies protein biomarkers and provides pathological insight.

Authors:  Stephanie M Cologna; Xiao-Sheng Jiang; Peter S Backlund; Celine V M Cluzeau; Michelle K Dail; Nicole M Yanjanin; Stephan Siebel; Cynthia L Toth; Hyun-sik Jun; Christopher A Wassif; Alfred L Yergey; Forbes D Porter
Journal:  PLoS One       Date:  2012-10-29       Impact factor: 3.240

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Journal:  PLoS One       Date:  2012-07-31       Impact factor: 3.240

9.  Comprehensive analysis of the mouse renal cortex using two-dimensional HPLC - tandem mass spectrometry.

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10.  Inhibition of transketolase by oxythiamine altered dynamics of protein signals in pancreatic cancer cells.

Authors:  Jiarui Wang; Danjun Ma; Xuemei Zhang; Wai-Nang Paul Lee; Jing Xiao; Yingchun Zhao; Vay Liang Go; Qi Wang; Yun Yen; Robert Recker; Gary Guishan Xiao
Journal:  Exp Hematol Oncol       Date:  2013-07-27
  10 in total

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