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Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex

Recent in vivo studies reveal that several membrane proteins are driven to form nanoclusters by active contractile flows arising from localized dynamic patterning of F-actin and myosin at the cortex. Since myosin-II assemble as minifilaments with tens of myosin heads, one might worry that steric con...

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Autores principales: Das, Amit, Bhat, Abrar, Sknepnek, Rastko, Köster, Darius, Mayor, Satyajit, Rao, Madan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065884/
https://www.ncbi.nlm.nih.gov/pubmed/32195346
http://dx.doi.org/10.1126/sciadv.aay6093
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author Das, Amit
Bhat, Abrar
Sknepnek, Rastko
Köster, Darius
Mayor, Satyajit
Rao, Madan
author_facet Das, Amit
Bhat, Abrar
Sknepnek, Rastko
Köster, Darius
Mayor, Satyajit
Rao, Madan
author_sort Das, Amit
collection PubMed
description Recent in vivo studies reveal that several membrane proteins are driven to form nanoclusters by active contractile flows arising from localized dynamic patterning of F-actin and myosin at the cortex. Since myosin-II assemble as minifilaments with tens of myosin heads, one might worry that steric considerations would obstruct the emergence of nanoclustering. Using coarse-grained, agent-based simulations that account for steric constraints, we find that the patterns exhibited by actomyosin in two dimensions, do not resemble the steady-state patterns in our in vitro reconstitution of actomyosin on a supported bilayer. We perform simulations in a thin rectangular slab, separating the layer of actin filaments from myosin-II minifilaments. This recapitulates the observed features of in vitro patterning. Using super resolution microscopy, we find evidence for such stratification in our in vitro system. Our study suggests that molecular stratification may be an important organizing feature of the cortical cytoskeleton in vivo.
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spelling pubmed-70658842020-03-19 Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex Das, Amit Bhat, Abrar Sknepnek, Rastko Köster, Darius Mayor, Satyajit Rao, Madan Sci Adv Research Articles Recent in vivo studies reveal that several membrane proteins are driven to form nanoclusters by active contractile flows arising from localized dynamic patterning of F-actin and myosin at the cortex. Since myosin-II assemble as minifilaments with tens of myosin heads, one might worry that steric considerations would obstruct the emergence of nanoclustering. Using coarse-grained, agent-based simulations that account for steric constraints, we find that the patterns exhibited by actomyosin in two dimensions, do not resemble the steady-state patterns in our in vitro reconstitution of actomyosin on a supported bilayer. We perform simulations in a thin rectangular slab, separating the layer of actin filaments from myosin-II minifilaments. This recapitulates the observed features of in vitro patterning. Using super resolution microscopy, we find evidence for such stratification in our in vitro system. Our study suggests that molecular stratification may be an important organizing feature of the cortical cytoskeleton in vivo. American Association for the Advancement of Science 2020-03-11 /pmc/articles/PMC7065884/ /pubmed/32195346 http://dx.doi.org/10.1126/sciadv.aay6093 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Das, Amit
Bhat, Abrar
Sknepnek, Rastko
Köster, Darius
Mayor, Satyajit
Rao, Madan
Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
title Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
title_full Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
title_fullStr Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
title_full_unstemmed Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
title_short Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
title_sort stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065884/
https://www.ncbi.nlm.nih.gov/pubmed/32195346
http://dx.doi.org/10.1126/sciadv.aay6093
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