Global Membrane Protein Interactome Analysis using In vivo Crosslinking and Mass Spectrometry-based Protein Correlation Profiling

被引:53
作者
Larance, Mark [1 ]
Kirkwood, Kathryn J. [1 ]
Tinti, Michele [2 ]
Murillo, Alejandro Brenes [1 ]
Ferguson, Michael A. J. [2 ]
Lamond, Angus I. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dow St, Dundee, Scotland
[2] Univ Dundee, Sch Life Sci, Biol Chem & Drug Discovery Div, Dundee, Scotland
基金
英国惠康基金;
关键词
DENSITY-LIPOPROTEIN RECEPTOR; HUMAN ACID CERAMIDASE; IDENTIFICATION; COMPLEXES; INTEGRIN; PURIFICATION; RESOURCE; SIZE;
D O I
10.1074/mcp.O115.055467
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a methodology using in vivo crosslinking combined with HPLC-MS for the global analysis of endogenous protein complexes by protein correlation profiling. Formaldehyde crosslinked protein complexes were extracted with high yield using denaturing buffers that maintained complex solubility during chromatographic separation. We show this efficiently detects both integral membrane and membrane-associated protein complexes, in addition to soluble complexes, allowing identification and analysis of complexes not accessible in native extracts. We compare the protein complexes detected by HPLC-MS protein correlation profiling in both native and formaldehyde crosslinked U2OS cell extracts. These proteome-wide data sets of both in vivo crosslinked and native protein complexes from U2OS cells are freely available via a searchable online database (www.peptracker. com/epd). Raw data are also available via Proteome-Xchange (identifier PXD003754).
引用
收藏
页码:2476 / 2490
页数:15
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