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A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes
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 p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818449/ https://www.ncbi.nlm.nih.gov/pubmed/36611993 http://dx.doi.org/10.3390/cells12010200 |
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author | Jia, Yunlong Reboulet, Jonathan Gillet, Benjamin Hughes, Sandrine Forcet, Christelle Tribollet, Violaine Hajj Sleiman, Nawal Kundlacz, Cindy Vanacker, Jean-Marc Bleicher, Françoise Merabet, Samir |
author_facet | Jia, Yunlong Reboulet, Jonathan Gillet, Benjamin Hughes, Sandrine Forcet, Christelle Tribollet, Violaine Hajj Sleiman, Nawal Kundlacz, Cindy Vanacker, Jean-Marc Bleicher, Françoise Merabet, Samir |
author_sort | Jia, Yunlong |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9818449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98184492023-01-07 A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes Jia, Yunlong Reboulet, Jonathan Gillet, Benjamin Hughes, Sandrine Forcet, Christelle Tribollet, Violaine Hajj Sleiman, Nawal Kundlacz, Cindy Vanacker, Jean-Marc Bleicher, Françoise Merabet, Samir Cells Article 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. MDPI 2023-01-03 /pmc/articles/PMC9818449/ /pubmed/36611993 http://dx.doi.org/10.3390/cells12010200 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jia, Yunlong Reboulet, Jonathan Gillet, Benjamin Hughes, Sandrine Forcet, Christelle Tribollet, Violaine Hajj Sleiman, Nawal Kundlacz, Cindy Vanacker, Jean-Marc Bleicher, Françoise Merabet, Samir A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes |
title | A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes |
title_full | A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes |
title_fullStr | A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes |
title_full_unstemmed | A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes |
title_short | A Live Cell Protein Complementation Assay for ORFeome-Wide Probing of Human HOX Interactomes |
title_sort | live cell protein complementation assay for orfeome-wide probing of human hox interactomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818449/ https://www.ncbi.nlm.nih.gov/pubmed/36611993 http://dx.doi.org/10.3390/cells12010200 |
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