pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides

Detalhes bibliográficos
Autor(a) principal: Tofanello, Aryane
Data de Publicação: 2016
Outros Autores: Miranda, Erica G. A., Dias, Igor W. R., Lanfredi, Alexandre J. C., Arantes, Jeverson T., Juliano, Maria A. [UNIFESP], Nantes, Iseli L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/51039
http://dx.doi.org/10.1021/acsomega.6b00140
Resumo: In the present study, alkaline peptides AAAXCX (X = lysine or arginine residues) were designed based on the conserved motif of the enzyme thioredoxin and used for the synthesis of gold nanoparticles (GNPs) in the pH range of 2-11. These peptides were compared with free cysteine, the counterpart acidic peptides AAAECE and gamma-ECG (glutathione), and the neutral peptide AAAACA. The objective was to investigate the effect of the amino acids neighboring a cysteine residue on the pH-dependent synthesis of gold nanocrystals. Kohn-Sham density functional theory (KS-DFT) calculations indicated an increase in the reducing capacity of AAAKCK favored by the successive deprotonation of their ionizable groups at increasing pH values. Experimentally, it was observed that gold speciation and the peptide structure also have a strong influence on the synthesis and stabilization of GNPs. AAAKCK produced GNPs at room temperature, in the whole investigated pH range. By contrast, alkaline pH was the best condition for the synthesis of GNP assisted by the AAARCR peptide. The acidic peptides produced GNPs only in the presence of polyethylene glycol, and the synthesis using AAAECE and gamma-ECG also required heating. The ionization state of AAAKCK had a strong influence on the preferential growth of the GNPs. Therefore, pH had a remarkable effect on the synthesis, kinetics, size, shape, and polydispersity of GNPs produced using AAAKCK. The AAAKCK peptide produced anisotropic decahedral and platelike nanocrystals at acidic pH values and spherical GNPs at alkaline pH values. Both alkaline peptides were also efficient capping agents for GNPs, but they produced a significant difference in the zeta potential, probably because of different orientations on the gold surface.
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spelling Tofanello, AryaneMiranda, Erica G. A.Dias, Igor W. R.Lanfredi, Alexandre J. C.Arantes, Jeverson T.Juliano, Maria A. [UNIFESP]Nantes, Iseli L.2019-07-22T15:46:43Z2019-07-22T15:46:43Z2016Acs Omega. Washington, v. 1, n. 3, p. 424-434, 2016.2470-1343http://repositorio.unifesp.br/handle/11600/51039http://dx.doi.org/10.1021/acsomega.6b00140WOS000391204000013.pdf10.1021/acsomega.6b00140WOS:000391204000013In the present study, alkaline peptides AAAXCX (X = lysine or arginine residues) were designed based on the conserved motif of the enzyme thioredoxin and used for the synthesis of gold nanoparticles (GNPs) in the pH range of 2-11. These peptides were compared with free cysteine, the counterpart acidic peptides AAAECE and gamma-ECG (glutathione), and the neutral peptide AAAACA. The objective was to investigate the effect of the amino acids neighboring a cysteine residue on the pH-dependent synthesis of gold nanocrystals. Kohn-Sham density functional theory (KS-DFT) calculations indicated an increase in the reducing capacity of AAAKCK favored by the successive deprotonation of their ionizable groups at increasing pH values. Experimentally, it was observed that gold speciation and the peptide structure also have a strong influence on the synthesis and stabilization of GNPs. AAAKCK produced GNPs at room temperature, in the whole investigated pH range. By contrast, alkaline pH was the best condition for the synthesis of GNP assisted by the AAARCR peptide. The acidic peptides produced GNPs only in the presence of polyethylene glycol, and the synthesis using AAAECE and gamma-ECG also required heating. The ionization state of AAAKCK had a strong influence on the preferential growth of the GNPs. Therefore, pH had a remarkable effect on the synthesis, kinetics, size, shape, and polydispersity of GNPs produced using AAAKCK. The AAAKCK peptide produced anisotropic decahedral and platelike nanocrystals at acidic pH values and spherical GNPs at alkaline pH values. Both alkaline peptides were also efficient capping agents for GNPs, but they produced a significant difference in the zeta potential, probably because of different orientations on the gold surface.FAPESP [2012/07456-7, 2015/17688-0]CNPqCAPES [5583/2014-04]Univ Fed ABC UFABC, CCNH, NanoBioMAv, Ave Estados 5001, BR-09210580 Sao Paulo, BrazilUniv Fed ABC UFABC, Ctr Engn Modelagem & Ciencias Sociais Aplicadas C, Ave Estados 5001, BR-09210580 Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Biol Mol, Rua 3 Maio 100,Vila Clementino, BR-04044020 Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Biol Mol, Rua 3 Maio 100,Vila Clementino, BR-04044020 Sao Paulo, BrazilFAPESP:2012/07456-72015/17688-0CAPES:5583/2014-04Web of Science424-434engAmer Chemical SocpH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptidesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/510392021-09-29 12:11:15.846metadata only accessoai:repositorio.unifesp.br:11600/51039Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-09-29T15:11:15Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
title pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
spellingShingle pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
Tofanello, Aryane
title_short pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
title_full pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
title_fullStr pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
title_full_unstemmed pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
title_sort pH-Dependent Synthesis of Anisotropic Gold Nanostructures by Bioinspired Cysteine-Containing Peptides
author Tofanello, Aryane
author_facet Tofanello, Aryane
Miranda, Erica G. A.
Dias, Igor W. R.
Lanfredi, Alexandre J. C.
Arantes, Jeverson T.
Juliano, Maria A. [UNIFESP]
Nantes, Iseli L.
author_role author
author2 Miranda, Erica G. A.
Dias, Igor W. R.
Lanfredi, Alexandre J. C.
Arantes, Jeverson T.
Juliano, Maria A. [UNIFESP]
Nantes, Iseli L.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Tofanello, Aryane
Miranda, Erica G. A.
Dias, Igor W. R.
Lanfredi, Alexandre J. C.
Arantes, Jeverson T.
Juliano, Maria A. [UNIFESP]
Nantes, Iseli L.
description In the present study, alkaline peptides AAAXCX (X = lysine or arginine residues) were designed based on the conserved motif of the enzyme thioredoxin and used for the synthesis of gold nanoparticles (GNPs) in the pH range of 2-11. These peptides were compared with free cysteine, the counterpart acidic peptides AAAECE and gamma-ECG (glutathione), and the neutral peptide AAAACA. The objective was to investigate the effect of the amino acids neighboring a cysteine residue on the pH-dependent synthesis of gold nanocrystals. Kohn-Sham density functional theory (KS-DFT) calculations indicated an increase in the reducing capacity of AAAKCK favored by the successive deprotonation of their ionizable groups at increasing pH values. Experimentally, it was observed that gold speciation and the peptide structure also have a strong influence on the synthesis and stabilization of GNPs. AAAKCK produced GNPs at room temperature, in the whole investigated pH range. By contrast, alkaline pH was the best condition for the synthesis of GNP assisted by the AAARCR peptide. The acidic peptides produced GNPs only in the presence of polyethylene glycol, and the synthesis using AAAECE and gamma-ECG also required heating. The ionization state of AAAKCK had a strong influence on the preferential growth of the GNPs. Therefore, pH had a remarkable effect on the synthesis, kinetics, size, shape, and polydispersity of GNPs produced using AAAKCK. The AAAKCK peptide produced anisotropic decahedral and platelike nanocrystals at acidic pH values and spherical GNPs at alkaline pH values. Both alkaline peptides were also efficient capping agents for GNPs, but they produced a significant difference in the zeta potential, probably because of different orientations on the gold surface.
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2019-07-22T15:46:43Z
dc.date.available.fl_str_mv 2019-07-22T15:46:43Z
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.citation.fl_str_mv Acs Omega. Washington, v. 1, n. 3, p. 424-434, 2016.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/51039
http://dx.doi.org/10.1021/acsomega.6b00140
dc.identifier.issn.none.fl_str_mv 2470-1343
dc.identifier.file.none.fl_str_mv WOS000391204000013.pdf
dc.identifier.doi.none.fl_str_mv 10.1021/acsomega.6b00140
dc.identifier.wos.none.fl_str_mv WOS:000391204000013
identifier_str_mv Acs Omega. Washington, v. 1, n. 3, p. 424-434, 2016.
2470-1343
WOS000391204000013.pdf
10.1021/acsomega.6b00140
WOS:000391204000013
url http://repositorio.unifesp.br/handle/11600/51039
http://dx.doi.org/10.1021/acsomega.6b00140
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 424-434
dc.publisher.none.fl_str_mv Amer Chemical Soc
publisher.none.fl_str_mv Amer Chemical Soc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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