Cargando…

Fluctuation of actin sliding over myosin thick filaments in vitro

It is customarily thought that myosin motors act as independent force-generators in both isotonic unloaded shortening as well as isometric contraction of muscle. We tested this assumption regarding unloaded shortening, by analyzing the fluctuation of the actin sliding movement over long native thick...

Descripción completa

Detalles Bibliográficos
Autores principales: Noda, Naoki, Imafuku, Yasuhiro, Yamada, Akira, Tawada, Katsuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society of Japan (BSJ) 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036633/
https://www.ncbi.nlm.nih.gov/pubmed/27857552
http://dx.doi.org/10.2142/biophysics.1.45
_version_ 1782455587936665600
author Noda, Naoki
Imafuku, Yasuhiro
Yamada, Akira
Tawada, Katsuhisa
author_facet Noda, Naoki
Imafuku, Yasuhiro
Yamada, Akira
Tawada, Katsuhisa
author_sort Noda, Naoki
collection PubMed
description It is customarily thought that myosin motors act as independent force-generators in both isotonic unloaded shortening as well as isometric contraction of muscle. We tested this assumption regarding unloaded shortening, by analyzing the fluctuation of the actin sliding movement over long native thick filaments from molluscan smooth muscle in vitro. This analysis is based on the prediction that the effective diffusion coefficient of actin, a measure of the fluctuation, is proportional to the inverse of the number of myosin motors generating the sliding movement of an actin filament, hence proportional to the inverse of the actin length, when the actions of the motors are stochastic and statistically independent. Contrary to this prediction, we found the effective diffusion coefficient to be virtually independent of, and thus not proportional to, the inverse of the actin length. This result shows that the myosin motors are not independent force-generators when generating the continuous sliding movement of actin in vitro and that the sliding motion is a macroscopic manifestation of the cooperative actions of the microscopic ensemble motors.
format Online
Article
Text
id pubmed-5036633
institution National Center for Biotechnology Information
language English
publishDate 2005
publisher The Biophysical Society of Japan (BSJ)
record_format MEDLINE/PubMed
spelling pubmed-50366332016-11-17 Fluctuation of actin sliding over myosin thick filaments in vitro Noda, Naoki Imafuku, Yasuhiro Yamada, Akira Tawada, Katsuhisa Biophysics (Nagoya-shi) Articles It is customarily thought that myosin motors act as independent force-generators in both isotonic unloaded shortening as well as isometric contraction of muscle. We tested this assumption regarding unloaded shortening, by analyzing the fluctuation of the actin sliding movement over long native thick filaments from molluscan smooth muscle in vitro. This analysis is based on the prediction that the effective diffusion coefficient of actin, a measure of the fluctuation, is proportional to the inverse of the number of myosin motors generating the sliding movement of an actin filament, hence proportional to the inverse of the actin length, when the actions of the motors are stochastic and statistically independent. Contrary to this prediction, we found the effective diffusion coefficient to be virtually independent of, and thus not proportional to, the inverse of the actin length. This result shows that the myosin motors are not independent force-generators when generating the continuous sliding movement of actin in vitro and that the sliding motion is a macroscopic manifestation of the cooperative actions of the microscopic ensemble motors. The Biophysical Society of Japan (BSJ) 2005-06-16 /pmc/articles/PMC5036633/ /pubmed/27857552 http://dx.doi.org/10.2142/biophysics.1.45 Text en 2005 © The Biophysical Society of Japan
spellingShingle Articles
Noda, Naoki
Imafuku, Yasuhiro
Yamada, Akira
Tawada, Katsuhisa
Fluctuation of actin sliding over myosin thick filaments in vitro
title Fluctuation of actin sliding over myosin thick filaments in vitro
title_full Fluctuation of actin sliding over myosin thick filaments in vitro
title_fullStr Fluctuation of actin sliding over myosin thick filaments in vitro
title_full_unstemmed Fluctuation of actin sliding over myosin thick filaments in vitro
title_short Fluctuation of actin sliding over myosin thick filaments in vitro
title_sort fluctuation of actin sliding over myosin thick filaments in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036633/
https://www.ncbi.nlm.nih.gov/pubmed/27857552
http://dx.doi.org/10.2142/biophysics.1.45
work_keys_str_mv AT nodanaoki fluctuationofactinslidingovermyosinthickfilamentsinvitro
AT imafukuyasuhiro fluctuationofactinslidingovermyosinthickfilamentsinvitro
AT yamadaakira fluctuationofactinslidingovermyosinthickfilamentsinvitro
AT tawadakatsuhisa fluctuationofactinslidingovermyosinthickfilamentsinvitro