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Entropic Tension in Crowded Membranes

Unlike their model membrane counterparts, biological membranes are richly decorated with a heterogeneous assembly of membrane proteins. These proteins are so tightly packed that their excluded area interactions can alter the free energy landscape controlling the conformational transitions suffered b...

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Detalles Bibliográficos
Autores principales: Lindén, Martin, Sens, Pierre, Phillips, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305330/
https://www.ncbi.nlm.nih.gov/pubmed/22438801
http://dx.doi.org/10.1371/journal.pcbi.1002431
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author Lindén, Martin
Sens, Pierre
Phillips, Rob
author_facet Lindén, Martin
Sens, Pierre
Phillips, Rob
author_sort Lindén, Martin
collection PubMed
description Unlike their model membrane counterparts, biological membranes are richly decorated with a heterogeneous assembly of membrane proteins. These proteins are so tightly packed that their excluded area interactions can alter the free energy landscape controlling the conformational transitions suffered by such proteins. For membrane channels, this effect can alter the critical membrane tension at which they undergo a transition from a closed to an open state, and therefore influence protein function in vivo. Despite their obvious importance, crowding phenomena in membranes are much less well studied than in the cytoplasm. Using statistical mechanics results for hard disk liquids, we show that crowding induces an entropic tension in the membrane, which influences transitions that alter the projected area and circumference of a membrane protein. As a specific case study in this effect, we consider the impact of crowding on the gating properties of bacterial mechanosensitive membrane channels, which are thought to confer osmoprotection when these cells are subjected to osmotic shock. We find that crowding can alter the gating energies by more than [Image: see text] in physiological conditions, a substantial fraction of the total gating energies in some cases. Given the ubiquity of membrane crowding, the nonspecific nature of excluded volume interactions, and the fact that the function of many membrane proteins involve significant conformational changes, this specific case study highlights a general aspect in the function of membrane proteins.
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spelling pubmed-33053302012-03-21 Entropic Tension in Crowded Membranes Lindén, Martin Sens, Pierre Phillips, Rob PLoS Comput Biol Research Article Unlike their model membrane counterparts, biological membranes are richly decorated with a heterogeneous assembly of membrane proteins. These proteins are so tightly packed that their excluded area interactions can alter the free energy landscape controlling the conformational transitions suffered by such proteins. For membrane channels, this effect can alter the critical membrane tension at which they undergo a transition from a closed to an open state, and therefore influence protein function in vivo. Despite their obvious importance, crowding phenomena in membranes are much less well studied than in the cytoplasm. Using statistical mechanics results for hard disk liquids, we show that crowding induces an entropic tension in the membrane, which influences transitions that alter the projected area and circumference of a membrane protein. As a specific case study in this effect, we consider the impact of crowding on the gating properties of bacterial mechanosensitive membrane channels, which are thought to confer osmoprotection when these cells are subjected to osmotic shock. We find that crowding can alter the gating energies by more than [Image: see text] in physiological conditions, a substantial fraction of the total gating energies in some cases. Given the ubiquity of membrane crowding, the nonspecific nature of excluded volume interactions, and the fact that the function of many membrane proteins involve significant conformational changes, this specific case study highlights a general aspect in the function of membrane proteins. Public Library of Science 2012-03-15 /pmc/articles/PMC3305330/ /pubmed/22438801 http://dx.doi.org/10.1371/journal.pcbi.1002431 Text en Lindén et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lindén, Martin
Sens, Pierre
Phillips, Rob
Entropic Tension in Crowded Membranes
title Entropic Tension in Crowded Membranes
title_full Entropic Tension in Crowded Membranes
title_fullStr Entropic Tension in Crowded Membranes
title_full_unstemmed Entropic Tension in Crowded Membranes
title_short Entropic Tension in Crowded Membranes
title_sort entropic tension in crowded membranes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305330/
https://www.ncbi.nlm.nih.gov/pubmed/22438801
http://dx.doi.org/10.1371/journal.pcbi.1002431
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