Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
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DOI:
10.1016/j.cell.2021.04.011
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发表时间:
2021-05-27
期刊:
影响因子:
64.5
通讯作者:
Gygi SP
Gygi SP
中科院分区:
生物学1区
文献类型:
--
作者:
Huttlin EL;Bruckner RJ;Navarrete-Perea J;Cannon JR;Baltier K;Gebreab F;Gygi MP;Thornock A;Zarraga G;Tam S;Szpyt J;Gassaway BM;Panov A;Parzen H;Fu S;Golbazi A;Maenpaa E;Stricker K;Guha Thakurta S;Zhang T;Rad R;Pan J;Nusinow DP;Paulo JA;Schweppe DK;Vaites LP;Harper JW;Gygi SP

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Thousands of interactions assemble proteins into modules that impart spatial and functional organization to the cellular proteome. Through affinity-purification mass spectrometry, we have created two proteome-scale, cell-line-specific interaction networks. The first, BioPlex 3.0, results from affinity purification of 10,128 human proteins – half the proteome – in 293T cells and includes 118,162 interactions among 14,586 proteins. The second results from 5,522 immunoprecipitations in HCT116 cells. These networks model the interactome whose structure encodes protein function, localization, and complex membership. Comparison across cell lines validates thousands of interactions and reveals extensive customization. While shared interactions reside in core complexes and involve essential proteins, cell-specific interactions link these complexes, ‘rewiring’ subnetworks within each cell’s interactome. Interactions covary among proteins of shared function as the proteome remodels to produce each cell’s phenotype. Viewable interactively online through BioPlexExplorer, these networks define principles of proteome organization and enable unknown protein characterization. Comparative analysis of large scale protein-protein interactions across two cell lines highlights context-specific interactions and proteome-scale shifts in how functional networks are arranged.
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