Development and application of wide-range gradient gel electrophoresis to proteome analysis

被引:6
|
作者
Yu, Hai [1 ]
Liu, Hui [1 ]
Yan, Yi-Zhong [1 ]
Dai, Zhi-Pan [1 ]
Yan, Shuai [1 ]
Li, Jiang-Lin [1 ]
Duan, Zhi-Gui [1 ]
Liu, Zhen [1 ]
Wang, Xian-Chun [1 ]
机构
[1] Hunan Normal Univ, Key Lab Prot Chem & Dev Biol, Minist Educ, Coll Life Sci, Changsha 410081, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
SODIUM DODECYL-SULFATE; INTEGRAL MEMBRANE-PROTEINS; HIGH-THROUGHPUT ANALYSIS; PLASMA-MEMBRANE; IDENTIFICATION; DIGESTION; REMOVAL; ENRICHMENT; DETERGENT; RECOVERY;
D O I
10.1039/c5ay01072a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
SDS is widely used to treat proteins that are difficult to solubilize and digest and improve protein separation in SDS-PAGE. However, SDS interferes with subsequent analyses and needs to be removed prior to digestion and LC-MS/MS analysis, whereas the conventional SDS-PAGE lacks the ability to efficiently remove SDS and retain low-molecular-weight proteins and peptides. In the present work, we developed a wide-range gradient gel electrophoresis (WGGE) system in a vertical slab gel electrophoresis cell, which was primarily composed of a 4-20% continuous gradient polyacrylamide gel separation layer and two interception layers with even higher concentrations (30% and 50%, respectively). The main advantages of the system are simultaneously cleaning up SDS-solubilized samples, separating proteins and intercepting low-molecular-weight proteins and peptides, thereby simplifying experimental operation, improving protein recovery and enhancing the total efficiency of proteome analysis. Using this system, about 87.25% of SDS in the sample and gel was electrophoretically removed and a peptide with a molecular weight of 3.75 kDa was efficiently intercepted. Combined with CapLC-MS/MS, the WGGE system was applied to the analysis of rat liver membrane-enriched protein samples and the results indicated that the WGGE-based strategy is suitable for the identification of proteins varying in molecular weight, pI, hydrophobicity, etc., suggesting potential applications in global and comparative analyses of various proteomes.
引用
收藏
页码:8109 / 8115
页数:7
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