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Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres
Rapid sarcomere lengthening waves propagate along a single muscle myofibril during spontaneous oscillatory contraction (SPOC). In asynchronous insect flight muscles, SPOC is thought to be almost completely synchronized over the entire myofibril. This phenomenon does not require Ca(2+) regulation of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6597731/ https://www.ncbi.nlm.nih.gov/pubmed/31249348 http://dx.doi.org/10.1038/s41598-019-45772-1 |
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author | Washio, Takumi Shintani, Seine A. Higuchi, Hideo Sugiura, Seiryo Hisada, Toshiaki |
author_facet | Washio, Takumi Shintani, Seine A. Higuchi, Hideo Sugiura, Seiryo Hisada, Toshiaki |
author_sort | Washio, Takumi |
collection | PubMed |
description | Rapid sarcomere lengthening waves propagate along a single muscle myofibril during spontaneous oscillatory contraction (SPOC). In asynchronous insect flight muscles, SPOC is thought to be almost completely synchronized over the entire myofibril. This phenomenon does not require Ca(2+) regulation of the dynamics of the motor proteins, and cannot be explained simply by the longitudinal mechanical equilibrium among sarcomeres in the myofibril. In the present study, we rationalize these phenomena by considering the lateral mechanical equilibrium, in which two tensions originating from the inverse relationship between sarcomere length and lattice spacing, along with the lattice alignment, play important roles in the mechanical communication between motor proteins on adjacent filaments via the Z-disc. The proposed model is capable of explaining various SPOC phenomena based on the stochastic power-stroke mechanism of motor proteins, which responds to temporal changes in longitudinal mechanical load. |
format | Online Article Text |
id | pubmed-6597731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65977312019-07-09 Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres Washio, Takumi Shintani, Seine A. Higuchi, Hideo Sugiura, Seiryo Hisada, Toshiaki Sci Rep Article Rapid sarcomere lengthening waves propagate along a single muscle myofibril during spontaneous oscillatory contraction (SPOC). In asynchronous insect flight muscles, SPOC is thought to be almost completely synchronized over the entire myofibril. This phenomenon does not require Ca(2+) regulation of the dynamics of the motor proteins, and cannot be explained simply by the longitudinal mechanical equilibrium among sarcomeres in the myofibril. In the present study, we rationalize these phenomena by considering the lateral mechanical equilibrium, in which two tensions originating from the inverse relationship between sarcomere length and lattice spacing, along with the lattice alignment, play important roles in the mechanical communication between motor proteins on adjacent filaments via the Z-disc. The proposed model is capable of explaining various SPOC phenomena based on the stochastic power-stroke mechanism of motor proteins, which responds to temporal changes in longitudinal mechanical load. Nature Publishing Group UK 2019-06-27 /pmc/articles/PMC6597731/ /pubmed/31249348 http://dx.doi.org/10.1038/s41598-019-45772-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Washio, Takumi Shintani, Seine A. Higuchi, Hideo Sugiura, Seiryo Hisada, Toshiaki Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
title | Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
title_full | Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
title_fullStr | Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
title_full_unstemmed | Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
title_short | Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
title_sort | effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6597731/ https://www.ncbi.nlm.nih.gov/pubmed/31249348 http://dx.doi.org/10.1038/s41598-019-45772-1 |
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