Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/membranes11050307 http://hdl.handle.net/11449/207689 |
Resumo: | Anionic lipid membrane electrostatic potential and solution pH can influence cationic peptide adsorption to these bilayers, especially those containing simultaneously acid and basic residues. Here, we investigate the effects of the pH solution on MP1 (IDWKKLLDAAKQIL-NH2) adsorption to anionic (7POPC:3POPG) lipid vesicles in comparison to its analog H-MP1, with histidines substituting lysines. We used the association of adsorption isotherms and constant pH molecular dynamic simulations (CpHMD) to explore the effects of membrane potential and pH on peptides’ adsorption on this lipid membrane. We analyzed the fluorescence and zeta potential adsorption isotherms using the Gouy–Chapman theory. In CpHMD simulations for the peptides in solution and adsorbed on the lipid bilayer, we used the conformations obtained by conventional MD simulations at a µs timescale. Non-equilibrium Monte Carlo simulations provided the protonation states of acidic and basic residues. CpHMD showed average pKa shifts of two to three units, resulting in a higher net charge for the analog than for MP1, strongly modulating the peptide adsorption. The fractions of the protonation of acidic and basic residues and the peptides’ net charges obtained from the analysis of the adsorption isotherms were in reasonable agreement with those from CpHMD. MP1 adsorption was almost insensitive to solution pH. H-MP1 was much more sensitive to partitioning, at acidic pH, with an affinity ten times higher than in neutral ones. |
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Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membraneCpHMDFluorescence spectroscopyMembrane potentialPH-responsive peptidesZeta potentialAnionic lipid membrane electrostatic potential and solution pH can influence cationic peptide adsorption to these bilayers, especially those containing simultaneously acid and basic residues. Here, we investigate the effects of the pH solution on MP1 (IDWKKLLDAAKQIL-NH2) adsorption to anionic (7POPC:3POPG) lipid vesicles in comparison to its analog H-MP1, with histidines substituting lysines. We used the association of adsorption isotherms and constant pH molecular dynamic simulations (CpHMD) to explore the effects of membrane potential and pH on peptides’ adsorption on this lipid membrane. We analyzed the fluorescence and zeta potential adsorption isotherms using the Gouy–Chapman theory. In CpHMD simulations for the peptides in solution and adsorbed on the lipid bilayer, we used the conformations obtained by conventional MD simulations at a µs timescale. Non-equilibrium Monte Carlo simulations provided the protonation states of acidic and basic residues. CpHMD showed average pKa shifts of two to three units, resulting in a higher net charge for the analog than for MP1, strongly modulating the peptide adsorption. The fractions of the protonation of acidic and basic residues and the peptides’ net charges obtained from the analysis of the adsorption isotherms were in reasonable agreement with those from CpHMD. MP1 adsorption was almost insensitive to solution pH. H-MP1 was much more sensitive to partitioning, at acidic pH, with an affinity ten times higher than in neutral ones.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)IBILCE Department of Physics UNESP—São Paulo State UniversityInstitute of Biosciences Department of Basic and Applied Biology UNESP—São Paulo State UniversityIBILCE Department of Physics UNESP—São Paulo State UniversityInstitute of Biosciences Department of Basic and Applied Biology UNESP—São Paulo State UniversityFAPESP: 2010/18169-3FAPESP: 2015/25619-9FAPESP: 2016/16212-5FAPESP: 2018/01841-2Universidade Estadual Paulista (Unesp)Alvares, Dayane Dos Santos [UNESP]Martins, Ingrid Bernardes Santana [UNESP]Viegas, Taisa Giordano [UNESP]Palma, Mario Sergio [UNESP]de Araujo, Alexandre Suman [UNESP]de Carvalho, Sidney Jurado [UNESP]Neto, João Ruggiero [UNESP]2021-06-25T10:59:22Z2021-06-25T10:59:22Z2021-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/membranes11050307Membranes, v. 11, n. 5, 2021.2077-0375http://hdl.handle.net/11449/20768910.3390/membranes110503072-s2.0-85105236077Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMembranesinfo:eu-repo/semantics/openAccess2021-10-23T17:45:55Zoai:repositorio.unesp.br:11449/207689Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:58:56.200934Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
title |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
spellingShingle |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane Alvares, Dayane Dos Santos [UNESP] CpHMD Fluorescence spectroscopy Membrane potential PH-responsive peptides Zeta potential |
title_short |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
title_full |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
title_fullStr |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
title_full_unstemmed |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
title_sort |
Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane |
author |
Alvares, Dayane Dos Santos [UNESP] |
author_facet |
Alvares, Dayane Dos Santos [UNESP] Martins, Ingrid Bernardes Santana [UNESP] Viegas, Taisa Giordano [UNESP] Palma, Mario Sergio [UNESP] de Araujo, Alexandre Suman [UNESP] de Carvalho, Sidney Jurado [UNESP] Neto, João Ruggiero [UNESP] |
author_role |
author |
author2 |
Martins, Ingrid Bernardes Santana [UNESP] Viegas, Taisa Giordano [UNESP] Palma, Mario Sergio [UNESP] de Araujo, Alexandre Suman [UNESP] de Carvalho, Sidney Jurado [UNESP] Neto, João Ruggiero [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Alvares, Dayane Dos Santos [UNESP] Martins, Ingrid Bernardes Santana [UNESP] Viegas, Taisa Giordano [UNESP] Palma, Mario Sergio [UNESP] de Araujo, Alexandre Suman [UNESP] de Carvalho, Sidney Jurado [UNESP] Neto, João Ruggiero [UNESP] |
dc.subject.por.fl_str_mv |
CpHMD Fluorescence spectroscopy Membrane potential PH-responsive peptides Zeta potential |
topic |
CpHMD Fluorescence spectroscopy Membrane potential PH-responsive peptides Zeta potential |
description |
Anionic lipid membrane electrostatic potential and solution pH can influence cationic peptide adsorption to these bilayers, especially those containing simultaneously acid and basic residues. Here, we investigate the effects of the pH solution on MP1 (IDWKKLLDAAKQIL-NH2) adsorption to anionic (7POPC:3POPG) lipid vesicles in comparison to its analog H-MP1, with histidines substituting lysines. We used the association of adsorption isotherms and constant pH molecular dynamic simulations (CpHMD) to explore the effects of membrane potential and pH on peptides’ adsorption on this lipid membrane. We analyzed the fluorescence and zeta potential adsorption isotherms using the Gouy–Chapman theory. In CpHMD simulations for the peptides in solution and adsorbed on the lipid bilayer, we used the conformations obtained by conventional MD simulations at a µs timescale. Non-equilibrium Monte Carlo simulations provided the protonation states of acidic and basic residues. CpHMD showed average pKa shifts of two to three units, resulting in a higher net charge for the analog than for MP1, strongly modulating the peptide adsorption. The fractions of the protonation of acidic and basic residues and the peptides’ net charges obtained from the analysis of the adsorption isotherms were in reasonable agreement with those from CpHMD. MP1 adsorption was almost insensitive to solution pH. H-MP1 was much more sensitive to partitioning, at acidic pH, with an affinity ten times higher than in neutral ones. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-25T10:59:22Z 2021-06-25T10:59:22Z 2021-05-01 |
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/10.3390/membranes11050307 Membranes, v. 11, n. 5, 2021. 2077-0375 http://hdl.handle.net/11449/207689 10.3390/membranes11050307 2-s2.0-85105236077 |
url |
http://dx.doi.org/10.3390/membranes11050307 http://hdl.handle.net/11449/207689 |
identifier_str_mv |
Membranes, v. 11, n. 5, 2021. 2077-0375 10.3390/membranes11050307 2-s2.0-85105236077 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Membranes |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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_ |
1808129270789177344 |