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OneOPES, a Combined Enhanced Sampling Method to Rule Them All
[Image: see text] Enhanced sampling techniques have revolutionized molecular dynamics (MD) simulations, enabling the study of rare events and the calculation of free energy differences in complex systems. One of the main families of enhanced sampling techniques uses physical degrees of freedom calle...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500989/ https://www.ncbi.nlm.nih.gov/pubmed/37603295 http://dx.doi.org/10.1021/acs.jctc.3c00254 |
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author | Rizzi, Valerio Aureli, Simone Ansari, Narjes Gervasio, Francesco Luigi |
author_facet | Rizzi, Valerio Aureli, Simone Ansari, Narjes Gervasio, Francesco Luigi |
author_sort | Rizzi, Valerio |
collection | PubMed |
description | [Image: see text] Enhanced sampling techniques have revolutionized molecular dynamics (MD) simulations, enabling the study of rare events and the calculation of free energy differences in complex systems. One of the main families of enhanced sampling techniques uses physical degrees of freedom called collective variables (CVs) to accelerate a system’s dynamics and recover the original system’s statistics. However, encoding all the relevant degrees of freedom in a limited number of CVs is challenging, particularly in large biophysical systems. Another category of techniques, such as parallel tempering, simulates multiple replicas of the system in parallel, without requiring CVs. However, these methods may explore less relevant high-energy portions of the phase space and become computationally expensive for large systems. To overcome the limitations of both approaches, we propose a replica exchange method called OneOPES that combines the power of multireplica simulations and CV-based enhanced sampling. This method efficiently accelerates the phase space sampling without the need for ideal CVs, extensive parameters fine tuning nor the use of a large number of replicas, as demonstrated by its successful applications to protein–ligand binding and protein folding benchmark systems. Our approach shows promise as a new direction in the development of enhanced sampling techniques for molecular dynamics simulations, providing an efficient and robust framework for the study of complex and unexplored problems. |
format | Online Article Text |
id | pubmed-10500989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105009892023-09-15 OneOPES, a Combined Enhanced Sampling Method to Rule Them All Rizzi, Valerio Aureli, Simone Ansari, Narjes Gervasio, Francesco Luigi J Chem Theory Comput [Image: see text] Enhanced sampling techniques have revolutionized molecular dynamics (MD) simulations, enabling the study of rare events and the calculation of free energy differences in complex systems. One of the main families of enhanced sampling techniques uses physical degrees of freedom called collective variables (CVs) to accelerate a system’s dynamics and recover the original system’s statistics. However, encoding all the relevant degrees of freedom in a limited number of CVs is challenging, particularly in large biophysical systems. Another category of techniques, such as parallel tempering, simulates multiple replicas of the system in parallel, without requiring CVs. However, these methods may explore less relevant high-energy portions of the phase space and become computationally expensive for large systems. To overcome the limitations of both approaches, we propose a replica exchange method called OneOPES that combines the power of multireplica simulations and CV-based enhanced sampling. This method efficiently accelerates the phase space sampling without the need for ideal CVs, extensive parameters fine tuning nor the use of a large number of replicas, as demonstrated by its successful applications to protein–ligand binding and protein folding benchmark systems. Our approach shows promise as a new direction in the development of enhanced sampling techniques for molecular dynamics simulations, providing an efficient and robust framework for the study of complex and unexplored problems. American Chemical Society 2023-08-21 /pmc/articles/PMC10500989/ /pubmed/37603295 http://dx.doi.org/10.1021/acs.jctc.3c00254 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Rizzi, Valerio Aureli, Simone Ansari, Narjes Gervasio, Francesco Luigi OneOPES, a Combined Enhanced Sampling Method to Rule Them All |
title | OneOPES, a Combined
Enhanced Sampling Method to Rule
Them All |
title_full | OneOPES, a Combined
Enhanced Sampling Method to Rule
Them All |
title_fullStr | OneOPES, a Combined
Enhanced Sampling Method to Rule
Them All |
title_full_unstemmed | OneOPES, a Combined
Enhanced Sampling Method to Rule
Them All |
title_short | OneOPES, a Combined
Enhanced Sampling Method to Rule
Them All |
title_sort | oneopes, a combined
enhanced sampling method to rule
them all |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500989/ https://www.ncbi.nlm.nih.gov/pubmed/37603295 http://dx.doi.org/10.1021/acs.jctc.3c00254 |
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