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Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies

Active matter systems can generate highly ordered structures, avoiding equilibrium through the consumption of energy by individual constituents. How the microscopic parameters that characterize the active agents are translated to the observed mesoscopic properties of the assembly has remained an ope...

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Autores principales: Banks, Rachel A, Galstyan, Vahe, Lee, Heun Jin, Hirokawa, Soichi, Ierokomos, Athena, Ross, Tyler D, Bryant, Zev, Thomson, Matt, Phillips, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014072/
https://www.ncbi.nlm.nih.gov/pubmed/36752605
http://dx.doi.org/10.7554/eLife.79402
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author Banks, Rachel A
Galstyan, Vahe
Lee, Heun Jin
Hirokawa, Soichi
Ierokomos, Athena
Ross, Tyler D
Bryant, Zev
Thomson, Matt
Phillips, Rob
author_facet Banks, Rachel A
Galstyan, Vahe
Lee, Heun Jin
Hirokawa, Soichi
Ierokomos, Athena
Ross, Tyler D
Bryant, Zev
Thomson, Matt
Phillips, Rob
author_sort Banks, Rachel A
collection PubMed
description Active matter systems can generate highly ordered structures, avoiding equilibrium through the consumption of energy by individual constituents. How the microscopic parameters that characterize the active agents are translated to the observed mesoscopic properties of the assembly has remained an open question. These active systems are prevalent in living matter; for example, in cells, the cytoskeleton is organized into structures such as the mitotic spindle through the coordinated activity of many motor proteins walking along microtubules. Here, we investigate how the microscopic motor-microtubule interactions affect the coherent structures formed in a reconstituted motor-microtubule system. This question is of deeper evolutionary significance as we suspect motor and microtubule type contribute to the shape and size of resulting structures. We explore key parameters experimentally and theoretically, using a variety of motors with different speeds, processivities, and directionalities. We demonstrate that aster size depends on the motor used to create the aster, and develop a model for the distribution of motors and microtubules in steady-state asters that depends on parameters related to motor speed and processivity. Further, we show that network contraction rates scale linearly with the single-motor speed in quasi-one-dimensional contraction experiments. In all, this theoretical and experimental work helps elucidate how microscopic motor properties are translated to the much larger scale of collective motor-microtubule assemblies.
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spelling pubmed-100140722023-03-15 Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies Banks, Rachel A Galstyan, Vahe Lee, Heun Jin Hirokawa, Soichi Ierokomos, Athena Ross, Tyler D Bryant, Zev Thomson, Matt Phillips, Rob eLife Physics of Living Systems Active matter systems can generate highly ordered structures, avoiding equilibrium through the consumption of energy by individual constituents. How the microscopic parameters that characterize the active agents are translated to the observed mesoscopic properties of the assembly has remained an open question. These active systems are prevalent in living matter; for example, in cells, the cytoskeleton is organized into structures such as the mitotic spindle through the coordinated activity of many motor proteins walking along microtubules. Here, we investigate how the microscopic motor-microtubule interactions affect the coherent structures formed in a reconstituted motor-microtubule system. This question is of deeper evolutionary significance as we suspect motor and microtubule type contribute to the shape and size of resulting structures. We explore key parameters experimentally and theoretically, using a variety of motors with different speeds, processivities, and directionalities. We demonstrate that aster size depends on the motor used to create the aster, and develop a model for the distribution of motors and microtubules in steady-state asters that depends on parameters related to motor speed and processivity. Further, we show that network contraction rates scale linearly with the single-motor speed in quasi-one-dimensional contraction experiments. In all, this theoretical and experimental work helps elucidate how microscopic motor properties are translated to the much larger scale of collective motor-microtubule assemblies. eLife Sciences Publications, Ltd 2023-02-08 /pmc/articles/PMC10014072/ /pubmed/36752605 http://dx.doi.org/10.7554/eLife.79402 Text en © 2023, Banks et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Physics of Living Systems
Banks, Rachel A
Galstyan, Vahe
Lee, Heun Jin
Hirokawa, Soichi
Ierokomos, Athena
Ross, Tyler D
Bryant, Zev
Thomson, Matt
Phillips, Rob
Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
title Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
title_full Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
title_fullStr Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
title_full_unstemmed Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
title_short Motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
title_sort motor processivity and speed determine structure and dynamics of microtubule-motor assemblies
topic Physics of Living Systems
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014072/
https://www.ncbi.nlm.nih.gov/pubmed/36752605
http://dx.doi.org/10.7554/eLife.79402
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