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Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies

For reconstruction of controlled cell division in a minimal cell model, or protocell, a positioning mechanism that spatially regulates division is indispensable. In Escherichia coli, the Min proteins oscillate from pole to pole to determine the division site by inhibition of the primary divisome pro...

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Detalles Bibliográficos
Autores principales: Kretschmer, Simon, Schwille, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284474/
https://www.ncbi.nlm.nih.gov/pubmed/25513760
http://dx.doi.org/10.3390/life4040915
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author Kretschmer, Simon
Schwille, Petra
author_facet Kretschmer, Simon
Schwille, Petra
author_sort Kretschmer, Simon
collection PubMed
description For reconstruction of controlled cell division in a minimal cell model, or protocell, a positioning mechanism that spatially regulates division is indispensable. In Escherichia coli, the Min proteins oscillate from pole to pole to determine the division site by inhibition of the primary divisome protein FtsZ anywhere but in the cell middle. Remarkably, when reconstituted under defined conditions in vitro, the Min proteins self-organize into spatiotemporal patterns in the presence of a lipid membrane and ATP. We review recent progress made in studying the Min system in vitro, particularly focusing on the effects of various physicochemical parameters and boundary conditions on pattern formation. Furthermore, we discuss implications and challenges for utilizing the Min system for division site placement in protocells.
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spelling pubmed-42844742015-01-21 Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies Kretschmer, Simon Schwille, Petra Life (Basel) Review For reconstruction of controlled cell division in a minimal cell model, or protocell, a positioning mechanism that spatially regulates division is indispensable. In Escherichia coli, the Min proteins oscillate from pole to pole to determine the division site by inhibition of the primary divisome protein FtsZ anywhere but in the cell middle. Remarkably, when reconstituted under defined conditions in vitro, the Min proteins self-organize into spatiotemporal patterns in the presence of a lipid membrane and ATP. We review recent progress made in studying the Min system in vitro, particularly focusing on the effects of various physicochemical parameters and boundary conditions on pattern formation. Furthermore, we discuss implications and challenges for utilizing the Min system for division site placement in protocells. MDPI 2014-12-11 /pmc/articles/PMC4284474/ /pubmed/25513760 http://dx.doi.org/10.3390/life4040915 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kretschmer, Simon
Schwille, Petra
Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies
title Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies
title_full Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies
title_fullStr Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies
title_full_unstemmed Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies
title_short Toward Spatially Regulated Division of Protocells: Insights into the E. coli Min System from in Vitro Studies
title_sort toward spatially regulated division of protocells: insights into the e. coli min system from in vitro studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284474/
https://www.ncbi.nlm.nih.gov/pubmed/25513760
http://dx.doi.org/10.3390/life4040915
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