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Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability

Biological membranes are composed of lipid bilayers that are often asymmetric with regards to the lipid composition and/or aqueous solvent they separate. Studying lipid asymmetry both experimentally and computationally is challenging. Molecular dynamics simulations of lipid bilayers with asymmetry a...

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Autores principales: Blumer, Madison, Harris, Sophia, Li, Mengzhe, Martinez, Luis, Untereiner, Michael, Saeta, Peter N., Carpenter, Timothy S., Ingólfsson, Helgi I., Bennett, W. F. Drew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396604/
https://www.ncbi.nlm.nih.gov/pubmed/32850783
http://dx.doi.org/10.3389/fcell.2020.00575
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author Blumer, Madison
Harris, Sophia
Li, Mengzhe
Martinez, Luis
Untereiner, Michael
Saeta, Peter N.
Carpenter, Timothy S.
Ingólfsson, Helgi I.
Bennett, W. F. Drew
author_facet Blumer, Madison
Harris, Sophia
Li, Mengzhe
Martinez, Luis
Untereiner, Michael
Saeta, Peter N.
Carpenter, Timothy S.
Ingólfsson, Helgi I.
Bennett, W. F. Drew
author_sort Blumer, Madison
collection PubMed
description Biological membranes are composed of lipid bilayers that are often asymmetric with regards to the lipid composition and/or aqueous solvent they separate. Studying lipid asymmetry both experimentally and computationally is challenging. Molecular dynamics simulations of lipid bilayers with asymmetry are difficult due to finite system sizes and time scales accessible to simulations. Due to the very slow flip-flop rate for phospholipids, one must first choose how many lipids are on each side of the bilayer, but the resulting bilayer may be unstable (or metastable) due to differing tensile and compressive forces between leaflets. Here we use molecular dynamics simulations to investigate a number of different asymmetric membrane systems, both with atomistic and coarse-grained models. Asymmetries studied include differences in number of lipids, lipid composition (unsaturated and saturated tails and different headgroups), and chemical gradients between the aqueous phases. Extensive analysis of the bilayers’ properties such as area per lipid, density, and lateral pressure profiles are used to characterize bilayer asymmetry. We also address how cholesterol (which flip-flops relatively quickly) influences membrane asymmetries. Our results show how each leaflet is influenced by the other and can mitigate the structural changes to the bilayer overall structure. Cholesterol can respond to changes in bilayer asymmetry to alleviate some of the effect on the bilayer structure, but that will alter its leaflet distribution, which in turn affects its chemical potential. Ionic imbalances are shown to have a modest change in bilayer structure, despite large changes in the electrostatic potential. Bilayer asymmetry can also induce a modest electrostatic potential across the membrane. Our results highlight the importance of membrane asymmetry on bilayer properties, the influence of lipid headgroups, tails and cholesterol on asymmetry, and the ability of lipids to adapt to different environments.
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spelling pubmed-73966042020-08-25 Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability Blumer, Madison Harris, Sophia Li, Mengzhe Martinez, Luis Untereiner, Michael Saeta, Peter N. Carpenter, Timothy S. Ingólfsson, Helgi I. Bennett, W. F. Drew Front Cell Dev Biol Cell and Developmental Biology Biological membranes are composed of lipid bilayers that are often asymmetric with regards to the lipid composition and/or aqueous solvent they separate. Studying lipid asymmetry both experimentally and computationally is challenging. Molecular dynamics simulations of lipid bilayers with asymmetry are difficult due to finite system sizes and time scales accessible to simulations. Due to the very slow flip-flop rate for phospholipids, one must first choose how many lipids are on each side of the bilayer, but the resulting bilayer may be unstable (or metastable) due to differing tensile and compressive forces between leaflets. Here we use molecular dynamics simulations to investigate a number of different asymmetric membrane systems, both with atomistic and coarse-grained models. Asymmetries studied include differences in number of lipids, lipid composition (unsaturated and saturated tails and different headgroups), and chemical gradients between the aqueous phases. Extensive analysis of the bilayers’ properties such as area per lipid, density, and lateral pressure profiles are used to characterize bilayer asymmetry. We also address how cholesterol (which flip-flops relatively quickly) influences membrane asymmetries. Our results show how each leaflet is influenced by the other and can mitigate the structural changes to the bilayer overall structure. Cholesterol can respond to changes in bilayer asymmetry to alleviate some of the effect on the bilayer structure, but that will alter its leaflet distribution, which in turn affects its chemical potential. Ionic imbalances are shown to have a modest change in bilayer structure, despite large changes in the electrostatic potential. Bilayer asymmetry can also induce a modest electrostatic potential across the membrane. Our results highlight the importance of membrane asymmetry on bilayer properties, the influence of lipid headgroups, tails and cholesterol on asymmetry, and the ability of lipids to adapt to different environments. Frontiers Media S.A. 2020-07-21 /pmc/articles/PMC7396604/ /pubmed/32850783 http://dx.doi.org/10.3389/fcell.2020.00575 Text en Copyright © 2020 Blumer, Harris, Li, Martinez, Untereiner, Saeta, Carpenter, Ingólfsson and Bennett. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Blumer, Madison
Harris, Sophia
Li, Mengzhe
Martinez, Luis
Untereiner, Michael
Saeta, Peter N.
Carpenter, Timothy S.
Ingólfsson, Helgi I.
Bennett, W. F. Drew
Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability
title Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability
title_full Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability
title_fullStr Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability
title_full_unstemmed Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability
title_short Simulations of Asymmetric Membranes Illustrate Cooperative Leaflet Coupling and Lipid Adaptability
title_sort simulations of asymmetric membranes illustrate cooperative leaflet coupling and lipid adaptability
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396604/
https://www.ncbi.nlm.nih.gov/pubmed/32850783
http://dx.doi.org/10.3389/fcell.2020.00575
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