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How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates

Protein binding often involves conformational changes. Important questions are whether a conformational change occurs prior to a binding event (‘conformational selection’) or after a binding event (‘induced fit’), and how conformational transition rates can be obtained from experiments. In this arti...

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Detalles Bibliográficos
Autores principales: Paul, Fabian, Weikl, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026370/
https://www.ncbi.nlm.nih.gov/pubmed/27636092
http://dx.doi.org/10.1371/journal.pcbi.1005067
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author Paul, Fabian
Weikl, Thomas R.
author_facet Paul, Fabian
Weikl, Thomas R.
author_sort Paul, Fabian
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description Protein binding often involves conformational changes. Important questions are whether a conformational change occurs prior to a binding event (‘conformational selection’) or after a binding event (‘induced fit’), and how conformational transition rates can be obtained from experiments. In this article, we present general results for the chemical relaxation rates of conformational-selection and induced-fit binding processes that hold for all concentrations of proteins and ligands and, thus, go beyond the standard pseudo-first-order approximation of large ligand concentration. These results allow to distinguish conformational-selection from induced-fit processes—also in cases in which such a distinction is not possible under pseudo-first-order conditions—and to extract conformational transition rates of proteins from chemical relaxation data.
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spelling pubmed-50263702016-09-27 How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates Paul, Fabian Weikl, Thomas R. PLoS Comput Biol Research Article Protein binding often involves conformational changes. Important questions are whether a conformational change occurs prior to a binding event (‘conformational selection’) or after a binding event (‘induced fit’), and how conformational transition rates can be obtained from experiments. In this article, we present general results for the chemical relaxation rates of conformational-selection and induced-fit binding processes that hold for all concentrations of proteins and ligands and, thus, go beyond the standard pseudo-first-order approximation of large ligand concentration. These results allow to distinguish conformational-selection from induced-fit processes—also in cases in which such a distinction is not possible under pseudo-first-order conditions—and to extract conformational transition rates of proteins from chemical relaxation data. Public Library of Science 2016-09-16 /pmc/articles/PMC5026370/ /pubmed/27636092 http://dx.doi.org/10.1371/journal.pcbi.1005067 Text en © 2016 Paul, Weikl http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Paul, Fabian
Weikl, Thomas R.
How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates
title How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates
title_full How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates
title_fullStr How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates
title_full_unstemmed How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates
title_short How to Distinguish Conformational Selection and Induced Fit Based on Chemical Relaxation Rates
title_sort how to distinguish conformational selection and induced fit based on chemical relaxation rates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026370/
https://www.ncbi.nlm.nih.gov/pubmed/27636092
http://dx.doi.org/10.1371/journal.pcbi.1005067
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