The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/38721 |
Resumo: | The study of the interaction between hair filaments and formulations or peptides is of utmost importance in fields like cosmetic research. Keratin intermediate filaments structure is not fully described, limiting the molecular dynamics (MD) studies in this field although its high potential to improve the area. We developed a computational model of a truncated protofibril, simulated its behavior in alcoholic based formulations and with one peptide. The simulations showed a strong interaction between the benzyl alcohol molecules of the formulations and the model, leading to the disorganization of the keratin chains, which regress with the removal of the alcohol molecules. This behavior can explain the increase of peptide uptake in hair shafts evidenced in fluorescence microscopy pictures. The model developed is valid to computationally reproduce the interaction between hair and alcoholic formulations and provide a robust base for new MD studies about hair properties. It is shown that the MD simulations can improve hair cosmetic research, improving the uptake of a compound of interest. |
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The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics dataScience & TechnologyThe study of the interaction between hair filaments and formulations or peptides is of utmost importance in fields like cosmetic research. Keratin intermediate filaments structure is not fully described, limiting the molecular dynamics (MD) studies in this field although its high potential to improve the area. We developed a computational model of a truncated protofibril, simulated its behavior in alcoholic based formulations and with one peptide. The simulations showed a strong interaction between the benzyl alcohol molecules of the formulations and the model, leading to the disorganization of the keratin chains, which regress with the removal of the alcohol molecules. This behavior can explain the increase of peptide uptake in hair shafts evidenced in fluorescence microscopy pictures. The model developed is valid to computationally reproduce the interaction between hair and alcoholic formulations and provide a robust base for new MD studies about hair properties. It is shown that the MD simulations can improve hair cosmetic research, improving the uptake of a compound of interest.Royal Society of ChemistryUniversidade do MinhoAntunes, José Egipto FerreiraCruz, Célia F.Azóia, Nuno G.Cavaco-Paulo, Artur2015-01-152015-01-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/38721engAntunes, J.; Cruz, Celia F; Azoia, Nuno G.; Paulo, Artur Cavaco, The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data. RSC Advances, 5(16), 12365-12371, 20152046-20692046-206910.1039/C4RA13901Ahttp://pubs.rsc.org/en/journals/journalissues/rainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:01:18Zoai:repositorium.sdum.uminho.pt:1822/38721Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:51:13.413480Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
title |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
spellingShingle |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data Antunes, José Egipto Ferreira Science & Technology |
title_short |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
title_full |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
title_fullStr |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
title_full_unstemmed |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
title_sort |
The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data |
author |
Antunes, José Egipto Ferreira |
author_facet |
Antunes, José Egipto Ferreira Cruz, Célia F. Azóia, Nuno G. Cavaco-Paulo, Artur |
author_role |
author |
author2 |
Cruz, Célia F. Azóia, Nuno G. Cavaco-Paulo, Artur |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Antunes, José Egipto Ferreira Cruz, Célia F. Azóia, Nuno G. Cavaco-Paulo, Artur |
dc.subject.por.fl_str_mv |
Science & Technology |
topic |
Science & Technology |
description |
The study of the interaction between hair filaments and formulations or peptides is of utmost importance in fields like cosmetic research. Keratin intermediate filaments structure is not fully described, limiting the molecular dynamics (MD) studies in this field although its high potential to improve the area. We developed a computational model of a truncated protofibril, simulated its behavior in alcoholic based formulations and with one peptide. The simulations showed a strong interaction between the benzyl alcohol molecules of the formulations and the model, leading to the disorganization of the keratin chains, which regress with the removal of the alcohol molecules. This behavior can explain the increase of peptide uptake in hair shafts evidenced in fluorescence microscopy pictures. The model developed is valid to computationally reproduce the interaction between hair and alcoholic formulations and provide a robust base for new MD studies about hair properties. It is shown that the MD simulations can improve hair cosmetic research, improving the uptake of a compound of interest. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-01-15 2015-01-15T00:00:00Z |
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://hdl.handle.net/1822/38721 |
url |
http://hdl.handle.net/1822/38721 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Antunes, J.; Cruz, Celia F; Azoia, Nuno G.; Paulo, Artur Cavaco, The effects of solvent composition on the affinity of a peptide towards hair keratin: experimental and molecular dynamics data. RSC Advances, 5(16), 12365-12371, 2015 2046-2069 2046-2069 10.1039/C4RA13901A http://pubs.rsc.org/en/journals/journalissues/ra |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Royal Society of Chemistry |
publisher.none.fl_str_mv |
Royal Society of Chemistry |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799132283919138816 |