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Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing
Nearly all mechanochemical models of the cross-bridge treat myosin as a simple linear spring arranged parallel to the contractile filaments. These single-spring models cannot account for the radial force that muscle generates (orthogonal to the long axis of the myofilaments) or the effects of change...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996315/ https://www.ncbi.nlm.nih.gov/pubmed/21152002 http://dx.doi.org/10.1371/journal.pcbi.1001018 |
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author | Williams, C. David Regnier, Michael Daniel, Thomas L. |
author_facet | Williams, C. David Regnier, Michael Daniel, Thomas L. |
author_sort | Williams, C. David |
collection | PubMed |
description | Nearly all mechanochemical models of the cross-bridge treat myosin as a simple linear spring arranged parallel to the contractile filaments. These single-spring models cannot account for the radial force that muscle generates (orthogonal to the long axis of the myofilaments) or the effects of changes in filament lattice spacing. We describe a more complex myosin cross-bridge model that uses multiple springs to replicate myosin's force-generating power stroke and account for the effects of lattice spacing and radial force. The four springs which comprise this model (the 4sXB) correspond to the mechanically relevant portions of myosin's structure. As occurs in vivo, the 4sXB's state-transition kinetics and force-production dynamics vary with lattice spacing. Additionally, we describe a simpler two-spring cross-bridge (2sXB) model which produces results similar to those of the 4sXB model. Unlike the 4sXB model, the 2sXB model requires no iterative techniques, making it more computationally efficient. The rate at which both multi-spring cross-bridges bind and generate force decreases as lattice spacing grows. The axial force generated by each cross-bridge as it undergoes a power stroke increases as lattice spacing grows. The radial force that a cross-bridge produces as it undergoes a power stroke varies from expansive to compressive as lattice spacing increases. Importantly, these results mirror those for intact, contracting muscle force production. |
format | Text |
id | pubmed-2996315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29963152010-12-10 Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing Williams, C. David Regnier, Michael Daniel, Thomas L. PLoS Comput Biol Research Article Nearly all mechanochemical models of the cross-bridge treat myosin as a simple linear spring arranged parallel to the contractile filaments. These single-spring models cannot account for the radial force that muscle generates (orthogonal to the long axis of the myofilaments) or the effects of changes in filament lattice spacing. We describe a more complex myosin cross-bridge model that uses multiple springs to replicate myosin's force-generating power stroke and account for the effects of lattice spacing and radial force. The four springs which comprise this model (the 4sXB) correspond to the mechanically relevant portions of myosin's structure. As occurs in vivo, the 4sXB's state-transition kinetics and force-production dynamics vary with lattice spacing. Additionally, we describe a simpler two-spring cross-bridge (2sXB) model which produces results similar to those of the 4sXB model. Unlike the 4sXB model, the 2sXB model requires no iterative techniques, making it more computationally efficient. The rate at which both multi-spring cross-bridges bind and generate force decreases as lattice spacing grows. The axial force generated by each cross-bridge as it undergoes a power stroke increases as lattice spacing grows. The radial force that a cross-bridge produces as it undergoes a power stroke varies from expansive to compressive as lattice spacing increases. Importantly, these results mirror those for intact, contracting muscle force production. Public Library of Science 2010-12-02 /pmc/articles/PMC2996315/ /pubmed/21152002 http://dx.doi.org/10.1371/journal.pcbi.1001018 Text en Williams et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Williams, C. David Regnier, Michael Daniel, Thomas L. Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing |
title | Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing |
title_full | Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing |
title_fullStr | Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing |
title_full_unstemmed | Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing |
title_short | Axial and Radial Forces of Cross-Bridges Depend on Lattice Spacing |
title_sort | axial and radial forces of cross-bridges depend on lattice spacing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996315/ https://www.ncbi.nlm.nih.gov/pubmed/21152002 http://dx.doi.org/10.1371/journal.pcbi.1001018 |
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