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Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions
14-3-3 proteins are a family of regulatory hubs that function through a vast network of protein-protein interactions. Their dysfunction or dysregulation is implicated in a wide range of diseases, and thus they are attractive drug targets, especially for molecular glues that promote protein-protein i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679655/ https://www.ncbi.nlm.nih.gov/pubmed/36425654 http://dx.doi.org/10.3389/fmolb.2022.1043673 |
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author | Thurairajah, Bethany Hudson, Andrew J. Doveston, Richard G. |
author_facet | Thurairajah, Bethany Hudson, Andrew J. Doveston, Richard G. |
author_sort | Thurairajah, Bethany |
collection | PubMed |
description | 14-3-3 proteins are a family of regulatory hubs that function through a vast network of protein-protein interactions. Their dysfunction or dysregulation is implicated in a wide range of diseases, and thus they are attractive drug targets, especially for molecular glues that promote protein-protein interactions for therapeutic intervention. However, an incomplete understanding of the molecular mechanisms that underpin 14-3-3 function hampers progress in drug design and development. Biophysical methodologies are an essential element of the 14-3-3 analytical toolbox, but in many cases have not been fully exploited. Here, we present a contemporary review of the predominant biophysical techniques used to study 14-3-3 protein-protein interactions, with a focus on examples that address key questions and challenges in the 14-3-3 field. |
format | Online Article Text |
id | pubmed-9679655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96796552022-11-23 Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions Thurairajah, Bethany Hudson, Andrew J. Doveston, Richard G. Front Mol Biosci Molecular Biosciences 14-3-3 proteins are a family of regulatory hubs that function through a vast network of protein-protein interactions. Their dysfunction or dysregulation is implicated in a wide range of diseases, and thus they are attractive drug targets, especially for molecular glues that promote protein-protein interactions for therapeutic intervention. However, an incomplete understanding of the molecular mechanisms that underpin 14-3-3 function hampers progress in drug design and development. Biophysical methodologies are an essential element of the 14-3-3 analytical toolbox, but in many cases have not been fully exploited. Here, we present a contemporary review of the predominant biophysical techniques used to study 14-3-3 protein-protein interactions, with a focus on examples that address key questions and challenges in the 14-3-3 field. Frontiers Media S.A. 2022-11-08 /pmc/articles/PMC9679655/ /pubmed/36425654 http://dx.doi.org/10.3389/fmolb.2022.1043673 Text en Copyright © 2022 Thurairajah, Hudson and Doveston. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Thurairajah, Bethany Hudson, Andrew J. Doveston, Richard G. Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
title | Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
title_full | Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
title_fullStr | Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
title_full_unstemmed | Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
title_short | Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
title_sort | contemporary biophysical approaches for studying 14-3-3 protein-protein interactions |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679655/ https://www.ncbi.nlm.nih.gov/pubmed/36425654 http://dx.doi.org/10.3389/fmolb.2022.1043673 |
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