Highlights on the capacities of "Gel-based" proteomics

被引:122
作者
Chevalier, Francois [1 ]
机构
[1] CEA, Prote Lab, IRCM, Fontenay Aux Roses, France
来源
PROTEOME SCIENCE | 2010年 / 8卷
关键词
IMMOBILIZED PH GRADIENTS; TRIS BATHOPHENANTHROLINE DISULFONATE; 2-DIMENSIONAL ELECTROPHORESIS GELS; LASER DESORPTION/IONIZATION-TIME; PLASMA-MEMBRANE PROTEINS; COOMASSIE BRILLIANT BLUE; OF-THE-ART; MASS-SPECTROMETRY; SYPRO-RUBY; FLUORESCENT DYES;
D O I
10.1186/1477-5956-8-23
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gel-based proteomic is the most popular and versatile method of global protein separation and quantification. This is a mature approach to screen the protein expression at the large scale, and a cheaper approach as compared with gel-free proteomics. Based on two independent biochemical characteristics of proteins, two-dimensional electrophoresis combines isoelectric focusing, which separates proteins according to their isoelectric point, and SDS-PAGE, which separates them further according to their molecular mass. The next typical steps of the flow of gel-based proteomics are spots visualization and evaluation, expression analysis and finally protein identification by mass spectrometry. For the study of differentially expressed proteins, two-dimensional electrophoresis allows simultaneously to detect, quantify and compare up to thousand protein spots isoforms, including post-translational modifications, in the same gel and in a wide range of biological systems. In this review article, the limits, benefits, and perspectives of gel-based proteomic approaches are discussed using concrete examples.
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页数:10
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