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Protein-fragment complementation assays for large-scale analysis of protein–protein interactions

Protein–protein interactions (PPIs) orchestrate nearly all biological processes. They are also considered attractive drug targets for treating many human diseases, including cancers and neurodegenerative disorders. Protein-fragment complementation assays (PCAs) provide a direct and straightforward w...

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Detalles Bibliográficos
Autores principales: Blaszczak, Ewa, Lazarewicz, Natalia, Sudevan, Aswani, Wysocki, Robert, Rabut, Gwenaël
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286835/
https://www.ncbi.nlm.nih.gov/pubmed/34156434
http://dx.doi.org/10.1042/BST20201058
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author Blaszczak, Ewa
Lazarewicz, Natalia
Sudevan, Aswani
Wysocki, Robert
Rabut, Gwenaël
author_facet Blaszczak, Ewa
Lazarewicz, Natalia
Sudevan, Aswani
Wysocki, Robert
Rabut, Gwenaël
author_sort Blaszczak, Ewa
collection PubMed
description Protein–protein interactions (PPIs) orchestrate nearly all biological processes. They are also considered attractive drug targets for treating many human diseases, including cancers and neurodegenerative disorders. Protein-fragment complementation assays (PCAs) provide a direct and straightforward way to study PPIs in living cells or multicellular organisms. Importantly, PCAs can be used to detect the interaction of proteins expressed at endogenous levels in their native cellular environment. In this review, we present the principle of PCAs and discuss some of their advantages and limitations. We describe their application in large-scale experiments to investigate PPI networks and to screen or profile PPI targeting compounds.
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spelling pubmed-82868352021-08-02 Protein-fragment complementation assays for large-scale analysis of protein–protein interactions Blaszczak, Ewa Lazarewicz, Natalia Sudevan, Aswani Wysocki, Robert Rabut, Gwenaël Biochem Soc Trans Review Articles Protein–protein interactions (PPIs) orchestrate nearly all biological processes. They are also considered attractive drug targets for treating many human diseases, including cancers and neurodegenerative disorders. Protein-fragment complementation assays (PCAs) provide a direct and straightforward way to study PPIs in living cells or multicellular organisms. Importantly, PCAs can be used to detect the interaction of proteins expressed at endogenous levels in their native cellular environment. In this review, we present the principle of PCAs and discuss some of their advantages and limitations. We describe their application in large-scale experiments to investigate PPI networks and to screen or profile PPI targeting compounds. Portland Press Ltd. 2021-06-30 2021-06-22 /pmc/articles/PMC8286835/ /pubmed/34156434 http://dx.doi.org/10.1042/BST20201058 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Articles
Blaszczak, Ewa
Lazarewicz, Natalia
Sudevan, Aswani
Wysocki, Robert
Rabut, Gwenaël
Protein-fragment complementation assays for large-scale analysis of protein–protein interactions
title Protein-fragment complementation assays for large-scale analysis of protein–protein interactions
title_full Protein-fragment complementation assays for large-scale analysis of protein–protein interactions
title_fullStr Protein-fragment complementation assays for large-scale analysis of protein–protein interactions
title_full_unstemmed Protein-fragment complementation assays for large-scale analysis of protein–protein interactions
title_short Protein-fragment complementation assays for large-scale analysis of protein–protein interactions
title_sort protein-fragment complementation assays for large-scale analysis of protein–protein interactions
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286835/
https://www.ncbi.nlm.nih.gov/pubmed/34156434
http://dx.doi.org/10.1042/BST20201058
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