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Structure-mechanics statistical learning uncovers mechanical relay in proteins
A protein's adaptive response to its substrates is one of the key questions driving molecular physics and physical chemistry. This work employs the recently developed structure-mechanics statistical learning method to establish a mechanical perspective. Specifically, by mapping all-atom molecul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966636/ https://www.ncbi.nlm.nih.gov/pubmed/35432911 http://dx.doi.org/10.1039/d1sc06184d |
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author | Raj, Nixon Click, Timothy H. Yang, Haw Chu, Jhih-Wei |
author_facet | Raj, Nixon Click, Timothy H. Yang, Haw Chu, Jhih-Wei |
author_sort | Raj, Nixon |
collection | PubMed |
description | A protein's adaptive response to its substrates is one of the key questions driving molecular physics and physical chemistry. This work employs the recently developed structure-mechanics statistical learning method to establish a mechanical perspective. Specifically, by mapping all-atom molecular dynamics simulations onto the spring parameters of a backbone-side-chain elastic network model, the chemical moiety specific force constants (or mechanical rigidity) are used to assemble the rigidity graph, which is the matrix of inter-residue coupling strength. Using the S1A protease and the PDZ3 signaling domain as examples, chains of spatially contiguous residues are found to exhibit prominent changes in their mechanical rigidity upon substrate binding or dissociation. Such a mechanical-relay picture thus provides a mechanistic underpinning for conformational changes, long-range communication, and inter-domain allostery in both proteins, where the responsive mechanical hotspots are mostly residues having important biological functions or significant mutation sensitivity. |
format | Online Article Text |
id | pubmed-8966636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89666362022-04-14 Structure-mechanics statistical learning uncovers mechanical relay in proteins Raj, Nixon Click, Timothy H. Yang, Haw Chu, Jhih-Wei Chem Sci Chemistry A protein's adaptive response to its substrates is one of the key questions driving molecular physics and physical chemistry. This work employs the recently developed structure-mechanics statistical learning method to establish a mechanical perspective. Specifically, by mapping all-atom molecular dynamics simulations onto the spring parameters of a backbone-side-chain elastic network model, the chemical moiety specific force constants (or mechanical rigidity) are used to assemble the rigidity graph, which is the matrix of inter-residue coupling strength. Using the S1A protease and the PDZ3 signaling domain as examples, chains of spatially contiguous residues are found to exhibit prominent changes in their mechanical rigidity upon substrate binding or dissociation. Such a mechanical-relay picture thus provides a mechanistic underpinning for conformational changes, long-range communication, and inter-domain allostery in both proteins, where the responsive mechanical hotspots are mostly residues having important biological functions or significant mutation sensitivity. The Royal Society of Chemistry 2022-01-19 /pmc/articles/PMC8966636/ /pubmed/35432911 http://dx.doi.org/10.1039/d1sc06184d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Raj, Nixon Click, Timothy H. Yang, Haw Chu, Jhih-Wei Structure-mechanics statistical learning uncovers mechanical relay in proteins |
title | Structure-mechanics statistical learning uncovers mechanical relay in proteins |
title_full | Structure-mechanics statistical learning uncovers mechanical relay in proteins |
title_fullStr | Structure-mechanics statistical learning uncovers mechanical relay in proteins |
title_full_unstemmed | Structure-mechanics statistical learning uncovers mechanical relay in proteins |
title_short | Structure-mechanics statistical learning uncovers mechanical relay in proteins |
title_sort | structure-mechanics statistical learning uncovers mechanical relay in proteins |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966636/ https://www.ncbi.nlm.nih.gov/pubmed/35432911 http://dx.doi.org/10.1039/d1sc06184d |
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