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Reconstitution of contractile actomyosin rings in vesicles
One of the grand challenges of bottom-up synthetic biology is the development of minimal machineries for cell division. The mechanical transformation of large-scale compartments, such as Giant Unilamellar Vesicles (GUVs), requires the geometry-specific coordination of active elements, several orders...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050101/ https://www.ncbi.nlm.nih.gov/pubmed/33859190 http://dx.doi.org/10.1038/s41467-021-22422-7 |
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author | Litschel, Thomas Kelley, Charlotte F. Holz, Danielle Adeli Koudehi, Maral Vogel, Sven K. Burbaum, Laura Mizuno, Naoko Vavylonis, Dimitrios Schwille, Petra |
author_facet | Litschel, Thomas Kelley, Charlotte F. Holz, Danielle Adeli Koudehi, Maral Vogel, Sven K. Burbaum, Laura Mizuno, Naoko Vavylonis, Dimitrios Schwille, Petra |
author_sort | Litschel, Thomas |
collection | PubMed |
description | One of the grand challenges of bottom-up synthetic biology is the development of minimal machineries for cell division. The mechanical transformation of large-scale compartments, such as Giant Unilamellar Vesicles (GUVs), requires the geometry-specific coordination of active elements, several orders of magnitude larger than the molecular scale. Of all cytoskeletal structures, large-scale actomyosin rings appear to be the most promising cellular elements to accomplish this task. Here, we have adopted advanced encapsulation methods to study bundled actin filaments in GUVs and compare our results with theoretical modeling. By changing few key parameters, actin polymerization can be differentiated to resemble various types of networks in living cells. Importantly, we find membrane binding to be crucial for the robust condensation into a single actin ring in spherical vesicles, as predicted by theoretical considerations. Upon force generation by ATP-driven myosin motors, these ring-like actin structures contract and locally constrict the vesicle, forming furrow-like deformations. On the other hand, cortex-like actin networks are shown to induce and stabilize deformations from spherical shapes. |
format | Online Article Text |
id | pubmed-8050101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80501012021-04-30 Reconstitution of contractile actomyosin rings in vesicles Litschel, Thomas Kelley, Charlotte F. Holz, Danielle Adeli Koudehi, Maral Vogel, Sven K. Burbaum, Laura Mizuno, Naoko Vavylonis, Dimitrios Schwille, Petra Nat Commun Article One of the grand challenges of bottom-up synthetic biology is the development of minimal machineries for cell division. The mechanical transformation of large-scale compartments, such as Giant Unilamellar Vesicles (GUVs), requires the geometry-specific coordination of active elements, several orders of magnitude larger than the molecular scale. Of all cytoskeletal structures, large-scale actomyosin rings appear to be the most promising cellular elements to accomplish this task. Here, we have adopted advanced encapsulation methods to study bundled actin filaments in GUVs and compare our results with theoretical modeling. By changing few key parameters, actin polymerization can be differentiated to resemble various types of networks in living cells. Importantly, we find membrane binding to be crucial for the robust condensation into a single actin ring in spherical vesicles, as predicted by theoretical considerations. Upon force generation by ATP-driven myosin motors, these ring-like actin structures contract and locally constrict the vesicle, forming furrow-like deformations. On the other hand, cortex-like actin networks are shown to induce and stabilize deformations from spherical shapes. Nature Publishing Group UK 2021-04-15 /pmc/articles/PMC8050101/ /pubmed/33859190 http://dx.doi.org/10.1038/s41467-021-22422-7 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Litschel, Thomas Kelley, Charlotte F. Holz, Danielle Adeli Koudehi, Maral Vogel, Sven K. Burbaum, Laura Mizuno, Naoko Vavylonis, Dimitrios Schwille, Petra Reconstitution of contractile actomyosin rings in vesicles |
title | Reconstitution of contractile actomyosin rings in vesicles |
title_full | Reconstitution of contractile actomyosin rings in vesicles |
title_fullStr | Reconstitution of contractile actomyosin rings in vesicles |
title_full_unstemmed | Reconstitution of contractile actomyosin rings in vesicles |
title_short | Reconstitution of contractile actomyosin rings in vesicles |
title_sort | reconstitution of contractile actomyosin rings in vesicles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050101/ https://www.ncbi.nlm.nih.gov/pubmed/33859190 http://dx.doi.org/10.1038/s41467-021-22422-7 |
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