Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model

Detalhes bibliográficos
Autor(a) principal: Downing, Rachel
Data de Publicação: 2020
Outros Autores: Volpe Bossa, Guilherme [UNESP], May, Sylvio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1039/d0sm00499e
http://hdl.handle.net/11449/198930
Resumo: Amphipathic peptides that partition into lipid bilayers affect the curvature elastic properties of their host. Some of these peptides are able to shift the Gaussian modulus to positive values, thus triggering an instability with respect to the formation of saddle curvatures. To characterize the generic aspects of the underlying mechanism, we employ a molecular lipid model that accounts for the interfacial tension between the polar and apolar regions of the membrane, for interactions between the lipid headgroups, and for the energy to stretch or compress the hydrocarbon chains. Peptides are modeled as cylinders that partition into the host membrane in a parallel orientation where they diminish the space available to the lipid headgroups and chains. The penetration depth into the membrane is determined by the angular size of the peptide's hydrophilic region. We demonstrate that only peptides with a small angular size of their hydrophilic region have an intrinsic tendency to render the Gaussian modulus more positive, and we identify conditions at which the Gaussian modulus adopts a positive sign upon increasing the peptide concentration. Our model allows us to also incorporate electrostatic interactions between cationic peptides and anionic lipids on the level of the linear Debye-Hückel model. We show that electrostatic interactions tend to shift the Gaussian modulus toward more positive values. Steric and electrostatic lipid-peptide interactions jointly decrease the effective interaction strength in the headgroup region of the host membrane thus suggesting a generic mechanisms of how certain amphipathic peptides are able to induce the formation of saddle curvatures.
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spelling Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular modelAmphipathic peptides that partition into lipid bilayers affect the curvature elastic properties of their host. Some of these peptides are able to shift the Gaussian modulus to positive values, thus triggering an instability with respect to the formation of saddle curvatures. To characterize the generic aspects of the underlying mechanism, we employ a molecular lipid model that accounts for the interfacial tension between the polar and apolar regions of the membrane, for interactions between the lipid headgroups, and for the energy to stretch or compress the hydrocarbon chains. Peptides are modeled as cylinders that partition into the host membrane in a parallel orientation where they diminish the space available to the lipid headgroups and chains. The penetration depth into the membrane is determined by the angular size of the peptide's hydrophilic region. We demonstrate that only peptides with a small angular size of their hydrophilic region have an intrinsic tendency to render the Gaussian modulus more positive, and we identify conditions at which the Gaussian modulus adopts a positive sign upon increasing the peptide concentration. Our model allows us to also incorporate electrostatic interactions between cationic peptides and anionic lipids on the level of the linear Debye-Hückel model. We show that electrostatic interactions tend to shift the Gaussian modulus toward more positive values. Steric and electrostatic lipid-peptide interactions jointly decrease the effective interaction strength in the headgroup region of the host membrane thus suggesting a generic mechanisms of how certain amphipathic peptides are able to induce the formation of saddle curvatures.Department of Physics North Dakota State UniversityDepartment of Physics São Paulo State University (UNESP) Institute of Biosciences Humanities and Exact SciencesDepartment of Physics São Paulo State University (UNESP) Institute of Biosciences Humanities and Exact SciencesNorth Dakota State UniversityUniversidade Estadual Paulista (Unesp)Downing, RachelVolpe Bossa, Guilherme [UNESP]May, Sylvio2020-12-12T01:25:51Z2020-12-12T01:25:51Z2020-06-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article5032-5043http://dx.doi.org/10.1039/d0sm00499eSoft Matter, v. 16, n. 21, p. 5032-5043, 2020.1744-68481744-683Xhttp://hdl.handle.net/11449/19893010.1039/d0sm00499e2-s2.0-85085929272Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengSoft Matterinfo:eu-repo/semantics/openAccess2021-10-22T21:03:10Zoai:repositorio.unesp.br:11449/198930Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:26:26.178225Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
title Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
spellingShingle Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
Downing, Rachel
title_short Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
title_full Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
title_fullStr Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
title_full_unstemmed Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
title_sort Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
author Downing, Rachel
author_facet Downing, Rachel
Volpe Bossa, Guilherme [UNESP]
May, Sylvio
author_role author
author2 Volpe Bossa, Guilherme [UNESP]
May, Sylvio
author2_role author
author
dc.contributor.none.fl_str_mv North Dakota State University
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Downing, Rachel
Volpe Bossa, Guilherme [UNESP]
May, Sylvio
description Amphipathic peptides that partition into lipid bilayers affect the curvature elastic properties of their host. Some of these peptides are able to shift the Gaussian modulus to positive values, thus triggering an instability with respect to the formation of saddle curvatures. To characterize the generic aspects of the underlying mechanism, we employ a molecular lipid model that accounts for the interfacial tension between the polar and apolar regions of the membrane, for interactions between the lipid headgroups, and for the energy to stretch or compress the hydrocarbon chains. Peptides are modeled as cylinders that partition into the host membrane in a parallel orientation where they diminish the space available to the lipid headgroups and chains. The penetration depth into the membrane is determined by the angular size of the peptide's hydrophilic region. We demonstrate that only peptides with a small angular size of their hydrophilic region have an intrinsic tendency to render the Gaussian modulus more positive, and we identify conditions at which the Gaussian modulus adopts a positive sign upon increasing the peptide concentration. Our model allows us to also incorporate electrostatic interactions between cationic peptides and anionic lipids on the level of the linear Debye-Hückel model. We show that electrostatic interactions tend to shift the Gaussian modulus toward more positive values. Steric and electrostatic lipid-peptide interactions jointly decrease the effective interaction strength in the headgroup region of the host membrane thus suggesting a generic mechanisms of how certain amphipathic peptides are able to induce the formation of saddle curvatures.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T01:25:51Z
2020-12-12T01:25:51Z
2020-06-07
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1039/d0sm00499e
Soft Matter, v. 16, n. 21, p. 5032-5043, 2020.
1744-6848
1744-683X
http://hdl.handle.net/11449/198930
10.1039/d0sm00499e
2-s2.0-85085929272
url http://dx.doi.org/10.1039/d0sm00499e
http://hdl.handle.net/11449/198930
identifier_str_mv Soft Matter, v. 16, n. 21, p. 5032-5043, 2020.
1744-6848
1744-683X
10.1039/d0sm00499e
2-s2.0-85085929272
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Soft Matter
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 5032-5043
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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