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Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association

The formation of functionally versatile protein complexes underlies almost every biological process. The estimation of how fast these complexes can be formed has broad implications for unravelling the mechanism of biomolecular recognition. This kinetic property is traditionally quantified by associa...

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Autores principales: Dhusia, Kalyani, Su, Zhaoqian, Wu, Yinghao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407674/
https://www.ncbi.nlm.nih.gov/pubmed/32679892
http://dx.doi.org/10.3390/biom10071056
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author Dhusia, Kalyani
Su, Zhaoqian
Wu, Yinghao
author_facet Dhusia, Kalyani
Su, Zhaoqian
Wu, Yinghao
author_sort Dhusia, Kalyani
collection PubMed
description The formation of functionally versatile protein complexes underlies almost every biological process. The estimation of how fast these complexes can be formed has broad implications for unravelling the mechanism of biomolecular recognition. This kinetic property is traditionally quantified by association rates, which can be measured through various experimental techniques. To complement these time-consuming and labor-intensive approaches, we developed a coarse-grained simulation approach to study the physical processes of protein–protein association. We systematically calibrated our simulation method against a large-scale benchmark set. By combining a physics-based force field with a statistically-derived potential in the simulation, we found that the association rates of more than 80% of protein complexes can be correctly predicted within one order of magnitude relative to their experimental measurements. We further showed that a mixture of force fields derived from complementary sources was able to describe the process of protein–protein association with mechanistic details. For instance, we show that association of a protein complex contains multiple steps in which proteins continuously search their local binding orientations and form non-native-like intermediates through repeated dissociation and re-association. Moreover, with an ensemble of loosely bound encounter complexes observed around their native conformation, we suggest that the transition states of protein–protein association could be highly diverse on the structural level. Our study also supports the idea in which the association of a protein complex is driven by a “funnel-like” energy landscape. In summary, these results shed light on our understanding of how protein–protein recognition is kinetically modulated, and our coarse-grained simulation approach can serve as a useful addition to the existing experimental approaches that measure protein–protein association rates.
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spelling pubmed-74076742020-08-12 Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association Dhusia, Kalyani Su, Zhaoqian Wu, Yinghao Biomolecules Article The formation of functionally versatile protein complexes underlies almost every biological process. The estimation of how fast these complexes can be formed has broad implications for unravelling the mechanism of biomolecular recognition. This kinetic property is traditionally quantified by association rates, which can be measured through various experimental techniques. To complement these time-consuming and labor-intensive approaches, we developed a coarse-grained simulation approach to study the physical processes of protein–protein association. We systematically calibrated our simulation method against a large-scale benchmark set. By combining a physics-based force field with a statistically-derived potential in the simulation, we found that the association rates of more than 80% of protein complexes can be correctly predicted within one order of magnitude relative to their experimental measurements. We further showed that a mixture of force fields derived from complementary sources was able to describe the process of protein–protein association with mechanistic details. For instance, we show that association of a protein complex contains multiple steps in which proteins continuously search their local binding orientations and form non-native-like intermediates through repeated dissociation and re-association. Moreover, with an ensemble of loosely bound encounter complexes observed around their native conformation, we suggest that the transition states of protein–protein association could be highly diverse on the structural level. Our study also supports the idea in which the association of a protein complex is driven by a “funnel-like” energy landscape. In summary, these results shed light on our understanding of how protein–protein recognition is kinetically modulated, and our coarse-grained simulation approach can serve as a useful addition to the existing experimental approaches that measure protein–protein association rates. MDPI 2020-07-15 /pmc/articles/PMC7407674/ /pubmed/32679892 http://dx.doi.org/10.3390/biom10071056 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dhusia, Kalyani
Su, Zhaoqian
Wu, Yinghao
Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association
title Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association
title_full Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association
title_fullStr Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association
title_full_unstemmed Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association
title_short Using Coarse-Grained Simulations to Characterize the Mechanisms of Protein–Protein Association
title_sort using coarse-grained simulations to characterize the mechanisms of protein–protein association
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407674/
https://www.ncbi.nlm.nih.gov/pubmed/32679892
http://dx.doi.org/10.3390/biom10071056
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