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Multifunctional biosensors based on peptide-polyelectrolyte conjugates.
Kogikoski, S; Sousa, C P; Liberato, M S; Andrade-Filho, T; Prieto, T; Ferreira, F F; Rocha, A R; Guha, S; Alves, W A.
Affiliation
  • Kogikoski S; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580, Santo André, SP, Brazil. wendel.alves@ufabc.edu.br.
  • Sousa CP; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580, Santo André, SP, Brazil. wendel.alves@ufabc.edu.br.
  • Liberato MS; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580, Santo André, SP, Brazil. wendel.alves@ufabc.edu.br.
  • Andrade-Filho T; Instituto de Ciências Exatas, Faculdade de Física, Universidade Federal do Sul e Sudeste do Pará, Campus Marabá, 68505-080, Marabá, Pará, Brazil.
  • Prieto T; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580, Santo André, SP, Brazil. wendel.alves@ufabc.edu.br.
  • Ferreira FF; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580, Santo André, SP, Brazil. wendel.alves@ufabc.edu.br.
  • Rocha AR; Instituto de Física Teórica, Universidade Estadual Paulista - UNESP, São Paulo, SP, Brazil.
  • Guha S; Department of Physics of Astronomy, University of Missouri, Columbia, Missouri 65211, USA.
  • Alves WA; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580, Santo André, SP, Brazil. wendel.alves@ufabc.edu.br.
Phys Chem Chem Phys ; 18(4): 3223-33, 2016 Jan 28.
Article in En | MEDLINE | ID: mdl-26744288
A novel enzymatic platform for the sensing of H2O2 and glucose that uses L,L-diphenylalanine micro/nanostructures (FF-MNSs) as an enzyme support is shown. This platform is obtained by the self-assembly of poly(allylamine hydrochloride) (PAH), FF-MNSs, and microperoxidase-11 (MP11) anchored onto the peptide matrix, in two different crystal structures of FF-MNSs: hexagonal (P61) and orthorhombic (P22121). The electroactive area of the electrodes increases in the presence of FF-MNSs. We also demonstrate via theoretical calculations that the valence band energy of the orthorhombic structure allows it to be doped, similarly to p-type semiconductors, where PAH acts as a doping agent for the orthorhombic peptide structure, decreasing the band-gap by around 1 eV, which results in a smaller charge transfer resistance. These results are consistent with electrochemical impedance spectroscopy measurements, which further elucidate the role of the band structure of the orthorhombic FF-MNSs in the conductivity and electron transfer rates of the hybrid material. An effective communication between the electrode and the active site of a glucose oxidase enzyme through MP11-protein complexes occurs, paving the way for FF-MNSs in the orthorhombic phase for the future development of bioelectronics sensing devices.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptides / Biosensing Techniques / Electrolytes Language: En Journal: Phys Chem Chem Phys Journal subject: BIOFISICA / QUIMICA Year: 2016 Document type: Article Affiliation country: Brazil Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptides / Biosensing Techniques / Electrolytes Language: En Journal: Phys Chem Chem Phys Journal subject: BIOFISICA / QUIMICA Year: 2016 Document type: Article Affiliation country: Brazil Country of publication: United kingdom