The BioPlex Network: A Systematic Exploration of the Human Interactome

被引:1033
作者
Huttlin, Edward L. [1 ]
Ting, Lily [1 ]
Bruckner, Raphael J. [1 ]
Gebreab, Fana [1 ]
Gygi, Melanie P. [1 ]
Szpyt, John [1 ]
Tam, Stanley [1 ]
Zarraga, Gabriela [1 ]
Colby, Greg [1 ]
Baltier, Kurt [1 ]
Dong, Rui [2 ,3 ]
Guarani, Virginia [1 ]
Vaites, Laura Pontano [1 ]
Ordureau, Alban [1 ]
Rad, Ramin [1 ]
Erickson, Brian K. [1 ]
Wuehr, Martin [1 ]
Chick, Joel [1 ]
Zhai, Bo [1 ]
Kolippakkam, Deepak [1 ]
Mintseris, Julian [1 ]
Obar, Robert A. [1 ,4 ]
Harris, Tim [4 ]
Artavanis-Tsakonas, Spyros [1 ,4 ]
Sowa, Mathew E. [1 ]
De Camilli, Pietro [2 ,3 ]
Paulo, Joao A. [1 ]
Harper, J. Wade [1 ]
Gygi, Steven P. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06519 USA
[3] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06519 USA
[4] Biogen, Cambridge, MA 02142 USA
关键词
PROTEIN COMPLEXES; LANDSCAPE; IDENTIFICATION; REVEALS;
D O I
10.1016/j.cell.2015.06.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein interactions form a network whose structure drives cellular function and whose organization informs biological inquiry. Using high-throughput affinity-purification mass spectrometry, we identify interacting partners for 2,594 human proteins in HEK293T cells. The resulting network (BioPlex) contains 23,744 interactions among 7,668 proteins with 86% previously undocumented. BioPlex accurately depicts known complexes, attaining 80%-100% coverage for most CORUM complexes. The network readily subdivides into communities that correspond to complexes or clusters of functionally related proteins. More generally, network architecture reflects cellular localization, biological process, and molecular function, enabling functional characterization of thousands of proteins. Network structure also reveals associations among thousands of protein domains, suggesting a basis for examining structurally related proteins. Finally, BioPlex, in combination with other approaches, can be used to reveal interactions of biological or clinical significance. For example, mutations in the membrane protein VAPB implicated in familial amyotrophic lateral sclerosis perturb a defined community of interactors.
引用
收藏
页码:425 / 440
页数:16
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