Biomaterial engineered electrodes for bioelectronics

Autor(en): Pardo-Yissar, V
Katz, E
Willner, I
Kotlyar, AB
Sanders, C
Lill, H
Stichwörter: 4-ELECTRON REDUCTION; AU-ELECTRODES; Chemistry; Chemistry, Physical; CYTOCHROME-C; DIOXYGEN; ELECTROCHEMICAL REDUCTION; ENZYME ELECTRODES; GLUCOSE-OXIDASE; GOLD ELECTRODE; KINETIC SEPARATION; MONOLAYERS
Erscheinungsdatum: 2000
Herausgeber: ROYAL SOC CHEMISTRY
Journal: FARADAY DISCUSSIONS
Volumen: 116
Startseite: 119
Seitenende: 134
Zusammenfassung: 
A series of single-cysteine-containing cytochrome c, Cyt c, heme proteins including the wild-type Cyt c (from Saccharomyces cerevisiae) and the mutants (V33C, Q21C, R18C, G1C, K9C and K4C) exhibit direct electrical contact with Au-electrodes upon covalent attachment to a maleimide monolayer associated with the electrode. With the G1C-Cyt c mutant, which includes the cysteine residue in the polypeptide chain at position 1, the potential-induced switchable control of the interfacial electron transfer was observed. This heme protein includes a positively charged protein periphery that surrounds the attachment site and faces the electrode surface. Biasing of the electrode at a negative potential (-0.3 V vs. SCE) attracts the reduced Fe(ii)-Cyt c heme protein to the electrode surface. Upon the application of a double-potential-step chronoamperometric signal onto the electrode, where the electrode potential is switched to 0.3 V and back to -0.3 V, the kinetics of the transient cathodic current, corresponding to the re-reduction of the Fe(iii)-Cyt c, is controlled by the time interval between the oxidative and reductive potential steps. While a short time interval results in a rapid interfacial electron-transfer, k(et)(1)=20 s(-1), long time intervals lead to a slow interfacial electron transfer to the Fe(iii)-Cyt c, k(et)(2)=1.5 s(-1). The fast interfacial electron-transfer rate-constant is attributed to the reduction of the surface-attracted Fe(iii)-Cyt c. The slow interfacial electron-transfer rate constant is attributed to the electrostatic repulsion of the positively charged Cyt c from the electrode surface, resulting in long-range electron transfer exhibiting a lower rate constant. At intermediate time intervals between the oxidative and reductive steps, two populations of Cyt c, consisting of surface-attracted and surface-repelled heme proteins, are observed. Crosslinking of a layered affinity complex between the Cyt c and cytochrome oxidase, COx, on an Au-electrode yields an electrically-contacted, integrated, electrode for the four-electron reduction of O-2 to water. Kinetic analysis reveals that the rate-limiting step in the bioelectrocatalytic reduction of O-2 by the integrated Cyt c/COx electrode is the primary electron transfer from the electrode support to the Cyt c units.
ISSN: 13596640
DOI: 10.1039/b001508n

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