Saddle-curvature instability of lipid bilayer induced by amphipathic peptides: a molecular model
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , |
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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Repositório Institucional da UNESP |
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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 |
|
_version_ |
1808129427175899136 |