A reference map of the human binary protein interactome.

["Luck K", "Kim DK", "Lambourne L", "Spirohn K", "Begg BE", "Bian W", "Brignall R", "Cafarelli T", "Campos-Laborie FJ", "Charloteaux B", "Choi D", "Coté AG", "Daley M", "Deimling S", "Desbuleux A", "Dricot A", "Gebbia M", "Hardy MF", "Kishore N", "Knapp JJ"]
Nature 2020
Open on PubMed

Global insights into cellular organization and genome function require comprehensive understanding of the interactome networks that mediate genotype-phenotype relationships<sup>1,2</sup>. Here we present a human 'all-by-all' reference interactome map of human binary protein interactions, or 'HuRI'. With approximately 53,000 protein-protein interactions, HuRI has approximately four times as many such interactions as there are high-quality curated interactions from small-scale studies. The integration of HuRI with genome<sup>3</sup>, transcriptome<sup>4</sup> and proteome<sup>5</sup> data enables cellular function to be studied within most physiological or pathological cellular contexts. We demonstrate the utility of HuRI in identifying the specific subcellular roles of protein-protein interactions. Inferred tissue-specific networks reveal general principles for the formation of cellular context-specific functions and elucidate potential molecular mechanisms that might underlie tissue-specific phenotypes of Mendelian diseases. HuRI is a systematic proteome-wide reference that links genomic variation to phenotypic outcomes.