Highlights on the capacities of "Gel-based" proteomics

被引:124
作者
Chevalier, Francois [1 ]
机构
[1] CEA, Prote Lab, IRCM, Fontenay Aux Roses, France
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
相关论文
共 99 条
[1]   Strategies for revealing lower abundance proteins in two-dimensional protein maps [J].
Ahmed, N ;
Rice, GE .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 815 (1-2) :39-50
[2]   Chromatographic and electrophoretic characterization of protein variants [J].
Ahrer, Karin ;
Jungbauer, Alois .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2006, 841 (1-2) :110-122
[3]   ISOELECTRIC-FOCUSING OF BASIC-PROTEINS - THE PROBLEM OF OXIDATION OF CYSTEINES [J].
ALTLAND, K ;
BECHER, P ;
ROSSMANN, U ;
BJELLQVIST, B .
ELECTROPHORESIS, 1988, 9 (09) :474-485
[4]   Mass spectral compatibility of four proteomics stains [J].
Ball, Malcolm S. ;
Karuso, Peter .
JOURNAL OF PROTEOME RESEARCH, 2007, 6 (11) :4313-4320
[5]  
Bergeron JJM, 2007, MOL CELL PROTEOMICS, V6, P1824
[6]   A luminescent ruthenium complex for ultrasensitive detection of proteins immobilized on membrane supports [J].
Berggren, K ;
Steinberg, TH ;
Lauber, WM ;
Carroll, JA ;
Lopez, MF ;
Chernokalskaya, E ;
Zieske, L ;
Diwu, ZJ ;
Haugland, RP ;
Patton, WF .
ANALYTICAL BIOCHEMISTRY, 1999, 276 (02) :129-143
[7]  
Berggren KN, 2002, PROTEOMICS, V2, P486, DOI 10.1002/1615-9861(200205)2:5<486::AID-PROT486>3.0.CO
[8]  
2-X
[9]   ISOELECTRIC-FOCUSING IN IMMOBILIZED PH GRADIENTS - PRINCIPLE, METHODOLOGY AND SOME APPLICATIONS [J].
BJELLQVIST, B ;
EK, K ;
RIGHETTI, PG ;
GIANAZZA, E ;
GORG, A ;
WESTERMEIER, R ;
POSTEL, W .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1982, 6 (04) :317-339
[10]  
Bouchal P, 2002, CHEM LISTY, V97, P29