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Actomyosin-Driven Division of a Synthetic Cell
[Image: see text] One of the major challenges of bottom-up synthetic biology is rebuilding a minimal cell division machinery. From a reconstitution perspective, the animal cell division apparatus is mechanically the simplest and therefore attractive to rebuild. An actin-based ring produces contracti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594324/ https://www.ncbi.nlm.nih.gov/pubmed/36164967 http://dx.doi.org/10.1021/acssynbio.2c00287 |
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author | Baldauf, Lucia van Buren, Lennard Fanalista, Federico Koenderink, Gijsje Hendrika |
author_facet | Baldauf, Lucia van Buren, Lennard Fanalista, Federico Koenderink, Gijsje Hendrika |
author_sort | Baldauf, Lucia |
collection | PubMed |
description | [Image: see text] One of the major challenges of bottom-up synthetic biology is rebuilding a minimal cell division machinery. From a reconstitution perspective, the animal cell division apparatus is mechanically the simplest and therefore attractive to rebuild. An actin-based ring produces contractile force to constrict the membrane. By contrast, microbes and plant cells have a cell wall, so division requires concerted membrane constriction and cell wall synthesis. Furthermore, reconstitution of the actin division machinery helps in understanding the physical and molecular mechanisms of cytokinesis in animal cells and thus our own cells. In this review, we describe the state-of-the-art research on reconstitution of minimal actin-mediated cytokinetic machineries. Based on the conceptual requirements that we obtained from the physics of the shape changes involved in cell division, we propose two major routes for building a minimal actin apparatus capable of division. Importantly, we acknowledge both the passive and active roles that the confining lipid membrane can play in synthetic cytokinesis. We conclude this review by identifying the most pressing challenges for future reconstitution work, thereby laying out a roadmap for building a synthetic cell equipped with a minimal actin division machinery. |
format | Online Article Text |
id | pubmed-9594324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95943242022-10-26 Actomyosin-Driven Division of a Synthetic Cell Baldauf, Lucia van Buren, Lennard Fanalista, Federico Koenderink, Gijsje Hendrika ACS Synth Biol [Image: see text] One of the major challenges of bottom-up synthetic biology is rebuilding a minimal cell division machinery. From a reconstitution perspective, the animal cell division apparatus is mechanically the simplest and therefore attractive to rebuild. An actin-based ring produces contractile force to constrict the membrane. By contrast, microbes and plant cells have a cell wall, so division requires concerted membrane constriction and cell wall synthesis. Furthermore, reconstitution of the actin division machinery helps in understanding the physical and molecular mechanisms of cytokinesis in animal cells and thus our own cells. In this review, we describe the state-of-the-art research on reconstitution of minimal actin-mediated cytokinetic machineries. Based on the conceptual requirements that we obtained from the physics of the shape changes involved in cell division, we propose two major routes for building a minimal actin apparatus capable of division. Importantly, we acknowledge both the passive and active roles that the confining lipid membrane can play in synthetic cytokinesis. We conclude this review by identifying the most pressing challenges for future reconstitution work, thereby laying out a roadmap for building a synthetic cell equipped with a minimal actin division machinery. American Chemical Society 2022-09-27 2022-10-21 /pmc/articles/PMC9594324/ /pubmed/36164967 http://dx.doi.org/10.1021/acssynbio.2c00287 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Baldauf, Lucia van Buren, Lennard Fanalista, Federico Koenderink, Gijsje Hendrika Actomyosin-Driven Division of a Synthetic Cell |
title | Actomyosin-Driven
Division of a Synthetic Cell |
title_full | Actomyosin-Driven
Division of a Synthetic Cell |
title_fullStr | Actomyosin-Driven
Division of a Synthetic Cell |
title_full_unstemmed | Actomyosin-Driven
Division of a Synthetic Cell |
title_short | Actomyosin-Driven
Division of a Synthetic Cell |
title_sort | actomyosin-driven
division of a synthetic cell |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594324/ https://www.ncbi.nlm.nih.gov/pubmed/36164967 http://dx.doi.org/10.1021/acssynbio.2c00287 |
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