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Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics

Biological membranes constantly modulate their fluidity for proper functioning of the cell. Modulation of membrane properties via regulation of fatty acid composition has gained a renewed interest owing to its relevance in endocytosis, endoplasmic reticulum membrane homeostasis, and adaptation mecha...

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Autores principales: Tyler, Arwen I. I., Greenfield, Jake L., Seddon, John M., Brooks, Nicholas J., Purushothaman, Sowmya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763698/
https://www.ncbi.nlm.nih.gov/pubmed/31616666
http://dx.doi.org/10.3389/fcell.2019.00187
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author Tyler, Arwen I. I.
Greenfield, Jake L.
Seddon, John M.
Brooks, Nicholas J.
Purushothaman, Sowmya
author_facet Tyler, Arwen I. I.
Greenfield, Jake L.
Seddon, John M.
Brooks, Nicholas J.
Purushothaman, Sowmya
author_sort Tyler, Arwen I. I.
collection PubMed
description Biological membranes constantly modulate their fluidity for proper functioning of the cell. Modulation of membrane properties via regulation of fatty acid composition has gained a renewed interest owing to its relevance in endocytosis, endoplasmic reticulum membrane homeostasis, and adaptation mechanisms in the deep sea. Endowed with significant degrees of freedom, the presence of free fatty acids can alter the curvature of membranes which in turn can alter the response of curvature sensing proteins, thus defining adaptive ways to reconfigure membranes. Most significantly, recent experiments demonstrated that polyunsaturated lipids facilitate membrane bending and fission by endocytic proteins – the first step in the biogenesis of synaptic vesicles. Despite the vital roles of fatty acids, a systematic study relating the interactions between fatty acids and membrane and the consequent effect on the bio-mechanics of membranes under the influence of fatty acids has been sparse. Of specific interest is the vast disparity in the properties of cis and trans fatty acids, that only differ in the orientation of the double bond and yet have entirely unique and opposing chemical properties. Here we demonstrate a combined X-ray diffraction and membrane fluctuation analysis method to couple the structural properties to the biophysical properties of fatty acid-laden membranes to address current gaps in our understanding. By systematically doping pure dioleoyl phosphatidylcholine (DOPC) membranes with cis fatty acid and trans fatty acid we demonstrate that the presence of fatty acids doesn’t always fluidize the membrane. Rather, an intricate balance between the curvature, molecular interactions, as well as the amount of specific fatty acid dictates the fluidity of membranes. Lower concentrations are dominated by the nature of interactions between the phospholipid and the fatty acids. Trans fatty acid increases the rigidity while decreasing the area per lipid similar to the properties depicted by the addition of saturated fatty acids to lipidic membranes. Cis fatty acid however displays the accepted view of having a fluidizing effect at small concentrations. At higher concentrations curvature frustration dominates, leading to increased rigidity irrespective of the type of fatty acid. These results are consistent with theoretical predictions as detailed in the manuscript.
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spelling pubmed-67636982019-10-15 Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics Tyler, Arwen I. I. Greenfield, Jake L. Seddon, John M. Brooks, Nicholas J. Purushothaman, Sowmya Front Cell Dev Biol Cell and Developmental Biology Biological membranes constantly modulate their fluidity for proper functioning of the cell. Modulation of membrane properties via regulation of fatty acid composition has gained a renewed interest owing to its relevance in endocytosis, endoplasmic reticulum membrane homeostasis, and adaptation mechanisms in the deep sea. Endowed with significant degrees of freedom, the presence of free fatty acids can alter the curvature of membranes which in turn can alter the response of curvature sensing proteins, thus defining adaptive ways to reconfigure membranes. Most significantly, recent experiments demonstrated that polyunsaturated lipids facilitate membrane bending and fission by endocytic proteins – the first step in the biogenesis of synaptic vesicles. Despite the vital roles of fatty acids, a systematic study relating the interactions between fatty acids and membrane and the consequent effect on the bio-mechanics of membranes under the influence of fatty acids has been sparse. Of specific interest is the vast disparity in the properties of cis and trans fatty acids, that only differ in the orientation of the double bond and yet have entirely unique and opposing chemical properties. Here we demonstrate a combined X-ray diffraction and membrane fluctuation analysis method to couple the structural properties to the biophysical properties of fatty acid-laden membranes to address current gaps in our understanding. By systematically doping pure dioleoyl phosphatidylcholine (DOPC) membranes with cis fatty acid and trans fatty acid we demonstrate that the presence of fatty acids doesn’t always fluidize the membrane. Rather, an intricate balance between the curvature, molecular interactions, as well as the amount of specific fatty acid dictates the fluidity of membranes. Lower concentrations are dominated by the nature of interactions between the phospholipid and the fatty acids. Trans fatty acid increases the rigidity while decreasing the area per lipid similar to the properties depicted by the addition of saturated fatty acids to lipidic membranes. Cis fatty acid however displays the accepted view of having a fluidizing effect at small concentrations. At higher concentrations curvature frustration dominates, leading to increased rigidity irrespective of the type of fatty acid. These results are consistent with theoretical predictions as detailed in the manuscript. Frontiers Media S.A. 2019-09-19 /pmc/articles/PMC6763698/ /pubmed/31616666 http://dx.doi.org/10.3389/fcell.2019.00187 Text en Copyright © 2019 Tyler, Greenfield, Seddon, Brooks and Purushothaman. 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
Tyler, Arwen I. I.
Greenfield, Jake L.
Seddon, John M.
Brooks, Nicholas J.
Purushothaman, Sowmya
Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics
title Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics
title_full Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics
title_fullStr Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics
title_full_unstemmed Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics
title_short Coupling Phase Behavior of Fatty Acid Containing Membranes to Membrane Bio-Mechanics
title_sort coupling phase behavior of fatty acid containing membranes to membrane bio-mechanics
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763698/
https://www.ncbi.nlm.nih.gov/pubmed/31616666
http://dx.doi.org/10.3389/fcell.2019.00187
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