Network-based prediction of protein interactions

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作者
István A. Kovács
Katja Luck
Kerstin Spirohn
Yang Wang
Carl Pollis
Sadie Schlabach
Wenting Bian
Dae-Kyum Kim
Nishka Kishore
Tong Hao
Michael A. Calderwood
Marc Vidal
Albert-László Barabási
机构
[1] Northeastern University,Network Science Institute and Department of Physics
[2] Center for Cancer Systems Biology (CCSB),Department of Genetics, Blavatnik Institute
[3] Dana-Farber Cancer Institute,Donnelly Centre, Toronto, Ontario, Canada, Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada, Department of Computer Science
[4] Wigner Research Centre for Physics,Division of Network Medicine and Department of Medicine
[5] Institute for Solid State Physics and Optics,Department of Network and Data Science
[6] Harvard Medical School,undefined
[7] University of Toronto,undefined
[8] Toronto,undefined
[9] Ontario,undefined
[10] Canada,undefined
[11] Lunenfeld-Tanenbaum Research Institute,undefined
[12] Sinai Health System,undefined
[13] Brigham and Women’s Hospital,undefined
[14] Harvard Medical School,undefined
[15] Central European University,undefined
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摘要
Despite exceptional experimental efforts to map out the human interactome, the continued data incompleteness limits our ability to understand the molecular roots of human disease. Computational tools offer a promising alternative, helping identify biologically significant, yet unmapped protein-protein interactions (PPIs). While link prediction methods connect proteins on the basis of biological or network-based similarity, interacting proteins are not necessarily similar and similar proteins do not necessarily interact. Here, we offer structural and evolutionary evidence that proteins interact not if they are similar to each other, but if one of them is similar to the other’s partners. This approach, that mathematically relies on network paths of length three (L3), significantly outperforms all existing link prediction methods. Given its high accuracy, we show that L3 can offer mechanistic insights into disease mechanisms and can complement future experimental efforts to complete the human interactome.
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