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Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology

Many intrinsically disordered peptides have been shown to undergo liquid–liquid phase separation and form complex coacervates, which play various regulatory roles in the cell. Recent experimental studies found that such phase separation processes may also occur at the lipid membrane surface and help...

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Autores principales: Mondal, Sayantan, Cui, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258347/
https://www.ncbi.nlm.nih.gov/pubmed/35865903
http://dx.doi.org/10.1039/d2sc02013k
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author Mondal, Sayantan
Cui, Qiang
author_facet Mondal, Sayantan
Cui, Qiang
author_sort Mondal, Sayantan
collection PubMed
description Many intrinsically disordered peptides have been shown to undergo liquid–liquid phase separation and form complex coacervates, which play various regulatory roles in the cell. Recent experimental studies found that such phase separation processes may also occur at the lipid membrane surface and help organize biomolecules during signaling events; in some cases, phase separation of proteins at the membrane surface was also observed to lead to significant remodeling of the membrane morphology. The molecular mechanisms that govern the interactions between complex coacervates and lipid membranes and the impacts of such interactions on their structure and morphology, however, remain unclear. Here we study the coacervation of poly-glutamate (E(30)) and poly-lysine (K(30)) in the presence of lipid bilayers of different compositions. We carry out explicit-solvent coarse-grained molecular dynamics simulations by using the MARTINI (v3.0) force-field. We find that more than 20% anionic lipids are required for the coacervate to form stable contact with the bilayer. Upon wetting, the coacervate induces negative curvature to the bilayer and facilitates local lipid demixing, without any peptide insertion. The magnitude of negative curvature, extent of lipid demixing, and asphericity of the coacervate increase with the concentration of anionic lipids. Overall, we observe a decrease in the number of contacts among the polyelectrolytes as the droplet spreads over the bilayer. Therefore, unlike previous suggestions, interactions among polyelectrolytes do not constitute a driving force for the membrane bending upon wetting by the coacervate. Rather, analysis of interaction energy components suggests that bending of the membrane is favored by enhanced interactions between polyelectrolytes with lipids as well as with counterions. Kinetic studies reveal that, at the studied polyelectrolyte concentrations, the coacervate formation precedes bilayer wetting.
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spelling pubmed-92583472022-07-20 Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology Mondal, Sayantan Cui, Qiang Chem Sci Chemistry Many intrinsically disordered peptides have been shown to undergo liquid–liquid phase separation and form complex coacervates, which play various regulatory roles in the cell. Recent experimental studies found that such phase separation processes may also occur at the lipid membrane surface and help organize biomolecules during signaling events; in some cases, phase separation of proteins at the membrane surface was also observed to lead to significant remodeling of the membrane morphology. The molecular mechanisms that govern the interactions between complex coacervates and lipid membranes and the impacts of such interactions on their structure and morphology, however, remain unclear. Here we study the coacervation of poly-glutamate (E(30)) and poly-lysine (K(30)) in the presence of lipid bilayers of different compositions. We carry out explicit-solvent coarse-grained molecular dynamics simulations by using the MARTINI (v3.0) force-field. We find that more than 20% anionic lipids are required for the coacervate to form stable contact with the bilayer. Upon wetting, the coacervate induces negative curvature to the bilayer and facilitates local lipid demixing, without any peptide insertion. The magnitude of negative curvature, extent of lipid demixing, and asphericity of the coacervate increase with the concentration of anionic lipids. Overall, we observe a decrease in the number of contacts among the polyelectrolytes as the droplet spreads over the bilayer. Therefore, unlike previous suggestions, interactions among polyelectrolytes do not constitute a driving force for the membrane bending upon wetting by the coacervate. Rather, analysis of interaction energy components suggests that bending of the membrane is favored by enhanced interactions between polyelectrolytes with lipids as well as with counterions. Kinetic studies reveal that, at the studied polyelectrolyte concentrations, the coacervate formation precedes bilayer wetting. The Royal Society of Chemistry 2022-06-16 /pmc/articles/PMC9258347/ /pubmed/35865903 http://dx.doi.org/10.1039/d2sc02013k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mondal, Sayantan
Cui, Qiang
Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
title Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
title_full Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
title_fullStr Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
title_full_unstemmed Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
title_short Coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
title_sort coacervation of poly-electrolytes in the presence of lipid bilayers: mutual alteration of structure and morphology
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258347/
https://www.ncbi.nlm.nih.gov/pubmed/35865903
http://dx.doi.org/10.1039/d2sc02013k
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