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Generalized Transition State Theory Treatment of Water-Assisted Proton Transport Processes in Proteins
[Image: see text] Transition state theory (TST) is widely employed for estimating the transition rate of a reaction when combined with free energy sampling techniques. A derivation of the transition theory rate expression for a general n-dimensional case is presented in this work which specifically...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762399/ https://www.ncbi.nlm.nih.gov/pubmed/36459423 http://dx.doi.org/10.1021/acs.jpcb.2c06703 |
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author | Liu, Yu Li, Chenghan Voth, Gregory A. |
author_facet | Liu, Yu Li, Chenghan Voth, Gregory A. |
author_sort | Liu, Yu |
collection | PubMed |
description | [Image: see text] Transition state theory (TST) is widely employed for estimating the transition rate of a reaction when combined with free energy sampling techniques. A derivation of the transition theory rate expression for a general n-dimensional case is presented in this work which specifically focuses on water-assisted proton transfer/transport reactions, especially for protein systems. Our work evaluates the TST prefactor calculated at the transition state dividing surface compared to one sampled, as an approximation, in the reactant state in four case studies of water-assisted proton transport inside membrane proteins and highlights the significant impact of the prefactor position dependence in proton transport processes. |
format | Online Article Text |
id | pubmed-9762399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97623992023-12-02 Generalized Transition State Theory Treatment of Water-Assisted Proton Transport Processes in Proteins Liu, Yu Li, Chenghan Voth, Gregory A. J Phys Chem B [Image: see text] Transition state theory (TST) is widely employed for estimating the transition rate of a reaction when combined with free energy sampling techniques. A derivation of the transition theory rate expression for a general n-dimensional case is presented in this work which specifically focuses on water-assisted proton transfer/transport reactions, especially for protein systems. Our work evaluates the TST prefactor calculated at the transition state dividing surface compared to one sampled, as an approximation, in the reactant state in four case studies of water-assisted proton transport inside membrane proteins and highlights the significant impact of the prefactor position dependence in proton transport processes. American Chemical Society 2022-12-02 2022-12-15 /pmc/articles/PMC9762399/ /pubmed/36459423 http://dx.doi.org/10.1021/acs.jpcb.2c06703 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Liu, Yu Li, Chenghan Voth, Gregory A. Generalized Transition State Theory Treatment of Water-Assisted Proton Transport Processes in Proteins |
title | Generalized Transition
State Theory Treatment of Water-Assisted
Proton Transport Processes in Proteins |
title_full | Generalized Transition
State Theory Treatment of Water-Assisted
Proton Transport Processes in Proteins |
title_fullStr | Generalized Transition
State Theory Treatment of Water-Assisted
Proton Transport Processes in Proteins |
title_full_unstemmed | Generalized Transition
State Theory Treatment of Water-Assisted
Proton Transport Processes in Proteins |
title_short | Generalized Transition
State Theory Treatment of Water-Assisted
Proton Transport Processes in Proteins |
title_sort | generalized transition
state theory treatment of water-assisted
proton transport processes in proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762399/ https://www.ncbi.nlm.nih.gov/pubmed/36459423 http://dx.doi.org/10.1021/acs.jpcb.2c06703 |
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