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Cellular self-organization: generating order from the abyss
While the organization of inanimate systems such as gases or liquids is predominantly thermodynamically driven—a mixture of two gases will tend to mix until they reach equilibrium—biological systems frequently exhibit organization that is far from a well-mixed equilibrium. The anisotropies displayed...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society for Cell Biology
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001480/ https://www.ncbi.nlm.nih.gov/pubmed/31999511 http://dx.doi.org/10.1091/mbc.E19-04-0207 |
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author | McCusker, Derek |
author_facet | McCusker, Derek |
author_sort | McCusker, Derek |
collection | PubMed |
description | While the organization of inanimate systems such as gases or liquids is predominantly thermodynamically driven—a mixture of two gases will tend to mix until they reach equilibrium—biological systems frequently exhibit organization that is far from a well-mixed equilibrium. The anisotropies displayed by cells are evident in some of the dynamic processes that constitute life including cell development, movement, and division. These anisotropies operate at different length-scales, from the meso- to the nanoscale, and are proposed to reflect self-organization, a characteristic of living systems that is becoming accessible to reconstitution from purified components, and thus a more thorough understanding. Here, some examples of self-organization underlying cellular anisotropies at the cellular level are reviewed, with an emphasis on Rho-family GTPases operating at the plasma membrane. Given the technical challenges of studying these dynamic proteins, some of the successful approaches that are being employed to study their self-organization will also be considered. |
format | Online Article Text |
id | pubmed-7001480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70014802020-06-06 Cellular self-organization: generating order from the abyss McCusker, Derek Mol Biol Cell Perspective While the organization of inanimate systems such as gases or liquids is predominantly thermodynamically driven—a mixture of two gases will tend to mix until they reach equilibrium—biological systems frequently exhibit organization that is far from a well-mixed equilibrium. The anisotropies displayed by cells are evident in some of the dynamic processes that constitute life including cell development, movement, and division. These anisotropies operate at different length-scales, from the meso- to the nanoscale, and are proposed to reflect self-organization, a characteristic of living systems that is becoming accessible to reconstitution from purified components, and thus a more thorough understanding. Here, some examples of self-organization underlying cellular anisotropies at the cellular level are reviewed, with an emphasis on Rho-family GTPases operating at the plasma membrane. Given the technical challenges of studying these dynamic proteins, some of the successful approaches that are being employed to study their self-organization will also be considered. The American Society for Cell Biology 2020-02-01 /pmc/articles/PMC7001480/ /pubmed/31999511 http://dx.doi.org/10.1091/mbc.E19-04-0207 Text en © 2020 McCusker. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Perspective McCusker, Derek Cellular self-organization: generating order from the abyss |
title | Cellular self-organization: generating order from the abyss |
title_full | Cellular self-organization: generating order from the abyss |
title_fullStr | Cellular self-organization: generating order from the abyss |
title_full_unstemmed | Cellular self-organization: generating order from the abyss |
title_short | Cellular self-organization: generating order from the abyss |
title_sort | cellular self-organization: generating order from the abyss |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001480/ https://www.ncbi.nlm.nih.gov/pubmed/31999511 http://dx.doi.org/10.1091/mbc.E19-04-0207 |
work_keys_str_mv | AT mccuskerderek cellularselforganizationgeneratingorderfromtheabyss |