Mapping the Protein Interaction Network of the Human COP9 Signalosome Complex Using a Label-free QTAX Strategy

被引:36
作者
Fang, Lei [1 ]
Kaake, Robyn M. [1 ]
Patel, Vishal R. [2 ]
Yang, Yingying [1 ]
Baldi, Pierre [2 ]
Huang, Lan [1 ]
机构
[1] Univ Calif Irvine, Dept Physiol & Biophys, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Comp Sci, Inst Genom & Bioinformat, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
AFFINITY PURIFICATION; COMPREHENSIVE RESOURCE; PROTEASOME; CULLIN; PROTEOMICS; GENETICS; KINASE; CORUM; SILAC; NEDD8;
D O I
10.1074/mcp.M111.016352
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The COP9 signalosome (CSN) is a multi-subunit protein complex that performs critical roles in controlling diverse cellular and developmental processes. Aberrant regulation of the CSN complex has been shown to lead to tumorigenesis. Despite its biological significance, our current knowledge of the function and regulation of the CSN complex is very limited. To explore CSN biology, we have developed and employed a new version of the tag team-based QTAX strategy (quantitative analysis of tandem affinity purified in vivo cross-linked (X) protein complexes) by incorporating a label-free MS method for quantitation. Coupled with protein interaction network analysis, this strategy produced a comprehensive and detailed assessment of the protein interaction network of the human CSN complex. In total, we quantitatively characterized 825 putative CSN-interacting proteins, with 270 classified as core interactors (captured by all three bait purifications). Biochemical validation further confirms the validity of selected identified interactors. This work presents the most complete analysis of the CSN interaction network to date, providing an inclusive set of physical interaction data consistent with physiological roles for the CSN. Moreover, the methodology described here is a general proteomic tool for the comprehensive study of protein interaction networks. Molecular & Cellular Proteomics 11: 10.1074/mcp.M111.016352, 138-147, 2012.
引用
收藏
页码:138 / 147
页数:10
相关论文
共 53 条
[1]   CSN5 isopeptidase activity links COP9 signalosome activation to breast cancer progression [J].
Adler, Adam S. ;
Littlepage, Laurie E. ;
Lin, Meihong ;
Kawahara, Tiara L. A. ;
Wong, David J. ;
Werb, Zena ;
Chang, Howard Y. .
CANCER RESEARCH, 2008, 68 (02) :506-515
[2]   Chemical genetics screen for enhancers of rapamycin identifies a specific inhibitor of an SCF family E3 ubiquitin ligase [J].
Aghajan, Mariam ;
Jonai, Nao ;
Flick, Karin ;
Fu, Fei ;
Luo, Manlin ;
Cai, Xiaolu ;
Ouni, Ikram ;
Pierce, Nathan ;
Tang, Xiaobo ;
Lomenick, Brett ;
Damoiseaux, Robert ;
Hao, Rui ;
del Moral, Pierre M. ;
Verma, Rati ;
Li, Ying ;
Li, Cheng ;
Houk, Kendall N. ;
Jung, Michael E. ;
Zheng, Ning ;
Huang, Lan ;
Deshaies, Raymond J. ;
Kaiser, Peter ;
Huang, Jing .
NATURE BIOTECHNOLOGY, 2010, 28 (07) :738-U1750
[3]   Dynamics of Cullin-RING Ubiquitin Ligase Network Revealed by Systematic Quantitative Proteomics [J].
Bennett, Eric J. ;
Rush, John ;
Gygi, Steven P. ;
Harper, J. Wade .
CELL, 2010, 143 (06) :951-965
[4]   Novel anti-angiogenic compounds for application in tumor therapy -: COP9 signalosome-associated kinases as possible targets [J].
Braumann, Chris ;
Tangermann, Judith ;
Jacobi, Christoph A. ;
Mueller, Joachim M. ;
Dubiel, Wolfgang .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2008, 8 (05) :421-428
[5]   A Global Protein Kinase and Phosphatase Interaction Network in Yeast [J].
Breitkreutz, Ashton ;
Choi, Hyungwon ;
Sharom, Jeffrey R. ;
Boucher, Lorrie ;
Neduva, Victor ;
Larsen, Brett ;
Lin, Zhen-Yuan ;
Breitkreutz, Bobby-Joe ;
Stark, Chris ;
Liu, Guomin ;
Ahn, Jessica ;
Dewar-Darch, Danielle ;
Reguly, Teresa ;
Tang, Xiaojing ;
Almeida, Ricardo ;
Qin, Zhaohui Steve ;
Pawson, Tony ;
Gingras, Anne-Claude ;
Nesvizhskii, Alexey I. ;
Tyers, Mike .
SCIENCE, 2010, 328 (5981) :1043-1046
[6]   SAINT: probabilistic scoring of affinity purification-mass spectrometry data [J].
Choi, Hyungwon ;
Larsen, Brett ;
Lin, Zhen-Yuan ;
Breitkreutz, Ashton ;
Mellacheruvu, Dattatreya ;
Fermin, Damian ;
Qin, Zhaohui S. ;
Tyers, Mike ;
Gingras, Anne-Claude ;
Nesvizhskii, Alexey I. .
NATURE METHODS, 2011, 8 (01) :70-U100
[7]   The Transmembrane Segment of a Tail-anchored Protein Determines Its Degradative Fate through Dislocation from the Endoplasmic Reticulum [J].
Claessen, Jasper H. L. ;
Mueller, Britta ;
Spooner, Eric ;
Pivorunas, Valerie L. ;
Ploegh, Hidde L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (27) :20732-20739
[8]   COP9 signalosome: A multifunctional regulator of SCF and other cullin-based ubiquitin Ligases [J].
Cope, GA ;
Deshaies, RJ .
CELL, 2003, 114 (06) :663-671
[9]   Role of predicted metalloprotease motif of Jab1/Csn5 in cleavage of Nedd8 from Cul1 [J].
Cope, GA ;
Suh, GSB ;
Aravind, L ;
Schwarz, SE ;
Zipursky, SL ;
Koonin, EV ;
Deshaies, RJ .
SCIENCE, 2002, 298 (5593) :608-611
[10]   RING Domain E3 Ubiquitin Ligases [J].
Deshaies, Raymond J. ;
Joazeiro, Claudio A. P. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2009, 78 :399-434