Modulatory effects of acidic ph and membrane potential on the adsorption of ph-sensitive peptides to anionic lipid membrane

Detalhes bibliográficos
Autor(a) principal: Alvares, Dayane Dos Santos [UNESP]
Data de Publicação: 2021
Outros Autores: 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]
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.
id UNSP_b74f124abc9bed2d4c17c105f62567ca
oai_identifier_str oai:repositorio.unesp.br:11449/207689
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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