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Illuminating the dark protein-protein interactome

In living systems, a complex network of protein-protein interactions (PPIs) underlies most biochemical events. The human protein-protein interactome has been surveyed using yeast two-hybrid (Y2H)- and mass spectrometry (MS)-based approaches such as affinity purification coupled to MS (AP-MS). Despit...

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Detalles Bibliográficos
Autores principales: Sharifi Tabar, Mehdi, Parsania, Chirag, Chen, Hong, Su, Xiao-Dong, Bailey, Charles G., Rasko, John E.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421580/
https://www.ncbi.nlm.nih.gov/pubmed/36046620
http://dx.doi.org/10.1016/j.crmeth.2022.100275
Descripción
Sumario:In living systems, a complex network of protein-protein interactions (PPIs) underlies most biochemical events. The human protein-protein interactome has been surveyed using yeast two-hybrid (Y2H)- and mass spectrometry (MS)-based approaches such as affinity purification coupled to MS (AP-MS). Despite decades of systematic investigations and collaborative multi-disciplinary efforts, there is no “gold standard” for documenting PPIs. A surprisingly large fraction of the human interactome remains uncharted, which we refer to as the “dark interactome.” In this review, we highlight the complexity of the human interactome and discuss the current status of the human reference interactome maps. We discuss why a large proportion of the human interactome has remained refractory to traditional approaches. We propose an experimental model that can enable the identification of the dark interactome in a cell-type-specific manner. We also propose a framework to implement when embarking on studies designed to rigorously identify and characterize protein interactions.