A Human IgSF Cell-Surface Interactome Reveals a Complex Network of Protein-Protein Interactions
Author(s) -
Woj M. Wojtowicz,
Jost Vielmetter,
Ricardo A. Fernandes,
Dirk H. Siepe,
Catharine Eastman,
Gregory B. Chisholm,
Sarah Cox,
Heath E. Klock,
Paul W. Anderson,
Sarah Rue,
Jessica M. Miller,
Scott Glaser,
Melisa L. Bragstad,
Julie Vance,
Annie W. Lam,
Scott A. Lesley,
Kai Zinn,
K. Christopher García
Publication year - 2020
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2020.07.025
Subject(s) - interactome , biology , computational biology , protein–protein interaction , surface protein , cell , microbiology and biotechnology , genetics , gene , virology
Cell-surface protein-protein interactions (PPIs) mediate cell-cell communication, recognition, and responses. We executed an interactome screen of 564 human cell-surface and secreted proteins, most of which are immunoglobulin superfamily (IgSF) proteins, using a high-throughput, automated ELISA-based screening platform employing a pooled-protein strategy to test all 318,096 PPI combinations. Screen results, augmented by phylogenetic homology analysis, revealed ∼380 previously unreported PPIs. We validated a subset using surface plasmon resonance and cell binding assays. Observed PPIs reveal a large and complex network of interactions both within and across biological systems. We identified new PPIs for receptors with well-characterized ligands and binding partners for "orphan" receptors. New PPIs include proteins expressed on multiple cell types and involved in diverse processes including immune and nervous system development and function, differentiation/proliferation, metabolism, vascularization, and reproduction. These PPIs provide a resource for further biological investigation into their functional relevance and may offer new therapeutic drug targets.
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