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The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism

Hsp70s use ATP to generate forces that disassemble protein complexes and aggregates, and that translocate proteins into organelles. Entropic pulling has been proposed as a novel mechanism, distinct from the more familiar power-stroke and Brownian ratchet models, for how Hsp70s generate these forces....

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Detalles Bibliográficos
Autores principales: Sousa, Rui, Lafer, Eileen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539501/
https://www.ncbi.nlm.nih.gov/pubmed/31083504
http://dx.doi.org/10.3390/ijms20092334
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author Sousa, Rui
Lafer, Eileen M.
author_facet Sousa, Rui
Lafer, Eileen M.
author_sort Sousa, Rui
collection PubMed
description Hsp70s use ATP to generate forces that disassemble protein complexes and aggregates, and that translocate proteins into organelles. Entropic pulling has been proposed as a novel mechanism, distinct from the more familiar power-stroke and Brownian ratchet models, for how Hsp70s generate these forces. Experimental evidence supports entropic pulling, but this model may not be well understood among scientists studying these systems. In this review we address persistent misconceptions regarding the dynamics of proteins in solution that contribute to this lack of understanding, and we clarify the basic physics of entropic pulling with some simple analogies. We hope that increased understanding of the entropic pulling mechanism will inform future efforts to characterize how Hsp70s function as motors, and how they coordinate with their regulatory cochaperones in mechanochemical cycles that transduce the energy of ATP hydrolysis into physical changes in their protein substrates.
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spelling pubmed-65395012019-06-04 The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism Sousa, Rui Lafer, Eileen M. Int J Mol Sci Review Hsp70s use ATP to generate forces that disassemble protein complexes and aggregates, and that translocate proteins into organelles. Entropic pulling has been proposed as a novel mechanism, distinct from the more familiar power-stroke and Brownian ratchet models, for how Hsp70s generate these forces. Experimental evidence supports entropic pulling, but this model may not be well understood among scientists studying these systems. In this review we address persistent misconceptions regarding the dynamics of proteins in solution that contribute to this lack of understanding, and we clarify the basic physics of entropic pulling with some simple analogies. We hope that increased understanding of the entropic pulling mechanism will inform future efforts to characterize how Hsp70s function as motors, and how they coordinate with their regulatory cochaperones in mechanochemical cycles that transduce the energy of ATP hydrolysis into physical changes in their protein substrates. MDPI 2019-05-11 /pmc/articles/PMC6539501/ /pubmed/31083504 http://dx.doi.org/10.3390/ijms20092334 Text en © 2019 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 Review
Sousa, Rui
Lafer, Eileen M.
The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism
title The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism
title_full The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism
title_fullStr The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism
title_full_unstemmed The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism
title_short The Physics of Entropic Pulling: A Novel Model for the Hsp70 Motor Mechanism
title_sort physics of entropic pulling: a novel model for the hsp70 motor mechanism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539501/
https://www.ncbi.nlm.nih.gov/pubmed/31083504
http://dx.doi.org/10.3390/ijms20092334
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