A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes

Cells. 2023 Jan 3;12(1):200. doi: 10.3390/cells12010200.

Abstract

Biological pathways rely on the formation of intricate protein interaction networks called interactomes. Getting a comprehensive map of interactomes implies the development of tools that allow one to capture transient and low-affinity protein-protein interactions (PPIs) in live conditions. Here we presented an experimental strategy: the Cell-PCA (cell-based protein complementation assay), which was based on bimolecular fluorescence complementation (BiFC) for ORFeome-wide screening of proteins that interact with different bait proteins in the same live cell context, by combining high-throughput sequencing method. The specificity and sensitivity of the Cell-PCA was established by using a wild-type and a single-amino-acid-mutated HOXA9 protein, and the approach was subsequently applied to seven additional human HOX proteins. These proof-of-concept experiments revealed novel molecular properties of HOX interactomes and led to the identification of a novel cofactor of HOXB13 that promoted its proliferative activity in a cancer cell context. Taken together, our work demonstrated that the Cell-PCA was pertinent for revealing and, importantly, comparing the interactomes of different or highly related bait proteins in the same cell context.

Keywords: BiFC; Cell-PCA; ORFeome-wide; human HOX proteins; live cells; protein-protein interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Microscopy, Fluorescence / methods
  • Protein Interaction Maps*

Grants and funding

This work was supported by the CNRS, ENS-Lyon, Fondation pour la Recherche Médicale (FRM #160896), Association pour la Recherche contre le Cancer (ARC #PJA20191209567), Ligue Régionale contre le Cancer (#119030) and Centre Franco-Indian pour la Promotion de la recherche Avancée (Cefipra #5503-P). Y.J. received a PhD grant from the China Scholarship Council (grant #201708070003).