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Toward an understanding of the regulation of myofibrillar function

Regulation of muscle contraction has been viewed as principally involving Ca(2+) binding to regulatory proteins on the thin filament, but while this is an important element of regulation, the mechanism does not explain the precise matching of muscle performance to the load it must lift or move. Now,...

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Detalles Bibliográficos
Autores principales: Moss, Richard L., de Tombe, Pieter P., Solaro, R. John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314381/
https://www.ncbi.nlm.nih.gov/pubmed/30578329
http://dx.doi.org/10.1085/jgp.201812288
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author Moss, Richard L.
de Tombe, Pieter P.
Solaro, R. John
author_facet Moss, Richard L.
de Tombe, Pieter P.
Solaro, R. John
author_sort Moss, Richard L.
collection PubMed
description Regulation of muscle contraction has been viewed as principally involving Ca(2+) binding to regulatory proteins on the thin filament, but while this is an important element of regulation, the mechanism does not explain the precise matching of muscle performance to the load it must lift or move. Now, it is increasingly evident that mechanisms instrinsic to the thick filament activate myosin cross-bridges as the force or load on a muscle increases. Both thick and thin filament regulatory mechanisms are featured in this special issue of the Journal of General Physiology.
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spelling pubmed-63143812019-07-07 Toward an understanding of the regulation of myofibrillar function Moss, Richard L. de Tombe, Pieter P. Solaro, R. John J Gen Physiol News Regulation of muscle contraction has been viewed as principally involving Ca(2+) binding to regulatory proteins on the thin filament, but while this is an important element of regulation, the mechanism does not explain the precise matching of muscle performance to the load it must lift or move. Now, it is increasingly evident that mechanisms instrinsic to the thick filament activate myosin cross-bridges as the force or load on a muscle increases. Both thick and thin filament regulatory mechanisms are featured in this special issue of the Journal of General Physiology. Rockefeller University Press 2019-01-07 /pmc/articles/PMC6314381/ /pubmed/30578329 http://dx.doi.org/10.1085/jgp.201812288 Text en © 2018 Moss et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle News
Moss, Richard L.
de Tombe, Pieter P.
Solaro, R. John
Toward an understanding of the regulation of myofibrillar function
title Toward an understanding of the regulation of myofibrillar function
title_full Toward an understanding of the regulation of myofibrillar function
title_fullStr Toward an understanding of the regulation of myofibrillar function
title_full_unstemmed Toward an understanding of the regulation of myofibrillar function
title_short Toward an understanding of the regulation of myofibrillar function
title_sort toward an understanding of the regulation of myofibrillar function
topic News
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314381/
https://www.ncbi.nlm.nih.gov/pubmed/30578329
http://dx.doi.org/10.1085/jgp.201812288
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