蛋白质组
生物发生
伴侣(临床)
免疫沉淀
生物化学
氧化还原酶
化学
聚丙烯酰胺凝胶电泳
蛋白质组学
生物
蛋白质-蛋白质相互作用
酶
医学
病理
基因
作者
Hans J. C. T. Wessels,Rutger O. Vogel,Lambert van den Heuvel,Jan A.M. Smeitink,Richard J. Rodenburg,Leo Nijtmans,Murtada H. Farhoud
出处
期刊:Proteomics
[Wiley]
日期:2009-08-17
卷期号:9 (17): 4221-4228
被引量:94
标识
DOI:10.1002/pmic.200900157
摘要
Abstract Two‐dimensional blue native/SDS‐PAGE is widely applied to investigate native protein–protein interactions, particularly those within membrane multi‐protein complexes. MS has enabled the application of this approach at the proteome scale, typically by analysis of picked protein spots. Here, we investigated the potential of using LC‐MS/MS as an alternative for SDS‐PAGE in blue native (BN) analysis of protein complexes. By subjecting equal slices from BN gel lanes to label‐free semi‐quantitative LC‐MS/MS, we determined an abundance profile for each protein across the BN gel, and used these profiles to identify potentially interacting proteins by protein correlation profiling. We demonstrate the feasibility of this approach by considering the oxidative phosphorylation complexes I–V in the native human embryonic kidney 293 mitochondrial fraction, showing that the method is capable of detecting both the fully assembled complexes as well as assembly/turnover intermediates of complex I (NADH:ubiquinone oxidoreductase). Using protein correlation profiling with a profile for subunits NDUFS2, 3, 7 and 8 we identified multiple proteins possibly involved in the biogenesis of complex I, including the recently implicated chaperone C6ORF66 and a novel candidate, C3ORF60.
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