Electrochemical studies on small electron transfer proteins using membrane electrodes

被引:37
作者
dos Santos, MMC
de Sousa, PMP
Gonçalves, MLS
Krippahl, L
Moura, JJG
Lojou, É
Bianco, P
机构
[1] Inst Super Tecn, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
[2] Univ Nova Lisboa, Fac Ciencias & Tecnol, Ctr Quim Fina & Biotecnol, REQUIMTE,Dept Quim, P-2825114 Monte De Caparica, Portugal
[3] CNRS, Unite Bioenerget & Ingn Prot, F-13402 Marseille 20, France
关键词
membrane electrodes; cytochromes c(552) and c(553); rubredoxin; unmediated electrochemistry;
D O I
10.1016/S0022-0728(02)01427-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Membrane electrodes (ME) were constructed using gold, glassy carbon and pyrolytic graphite supports and a dialysis membrane, and used to study the electrochemical behavior of small size electron transfer proteins: monohemic cytochrome c(522) from Pseudomonas nautica and cytochrome c(533) as well as rubredoxin from Desulfovibrio vulgaris. Different electrochemical techniques were used including cyclic voltammetry (CV), square wave voltammetry (SW) and differential pulse voltammetry (DP). A direct electrochemical response was obtained in all cases except with rubredoxin where a facilitator was added to the protein solution entrapped between the membrane and the electrode surface. Formal potentials and heterogeneous charge transfer rate constants were determined from the voltammetric data. The influence of the ionic strength and the pH of the medium on the electrochemical response at the ME were analyzed. The benefits from the use of the ME in protein electrochemistry and its role in modulating the redox behavior are analyzed. A critical comparison is presented with data obtained at non-MEs. Finally, the interactions that must be established between the proteins and the electrode surfaces are discussed, thereby modeling molecular interactions that occur in biological systems. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 162
页数:10
相关论文
共 37 条
[1]   The transient nature of the diffusion controlled component of the electrochemistry of cytochrome c at 'bare' gold electrodes: an explanation based on a self-blocking mechanism [J].
Allen, H ;
Hill, O ;
Hunt, NI ;
Bond, AM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1997, 436 (1-2) :17-25
[2]   SURFACE MODIFIERS FOR THE PROMOTION OF DIRECT ELECTROCHEMISTRY OF CYTOCHROME-C [J].
ALLEN, PM ;
HILL, HAO ;
WALTON, NJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 178 (01) :69-86
[3]   CHARACTERIZATION OF NERNSTIAN SQUARE-WAVE VOLTAMMOGRAMS [J].
AOKI, K ;
MAEDA, K ;
OSTERYOUNG, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 272 (1-2) :17-28
[4]   DIRECT ELECTROCHEMISTRY OF REDOX PROTEINS [J].
ARMSTRONG, FA ;
HILL, HAO ;
WALTON, NJ .
ACCOUNTS OF CHEMICAL RESEARCH, 1988, 21 (11) :407-413
[5]   Recent developments in faradaic bioelectrochemistry [J].
Armstrong, FA ;
Wilson, GS .
ELECTROCHIMICA ACTA, 2000, 45 (15-16) :2623-2645
[6]   ELECTROCHEMISTRY OF CYTOCHROME-C, PLASTOCYANIN, AND FERREDOXIN AT EDGE-PLANE AND BASAL-PLANE GRAPHITE-ELECTRODES INTERPRETED VIA A MODEL BASED ON ELECTRON-TRANSFER AT ELECTROACTIVE SITES OF MICROSCOPIC DIMENSIONS IN SIZE [J].
ARMSTRONG, FA ;
BOND, AM ;
HILL, HAO ;
OLIVER, BN ;
PSALTI, ISM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (26) :9185-9189
[7]   A MICROSCOPIC MODEL OF ELECTRON-TRANSFER AT ELECTROACTIVE SITES OF MOLECULAR DIMENSIONS FOR REDUCTION OF CYTOCHROME-C AT BASAL-PLANE AND EDGE-PLANE GRAPHITE-ELECTRODES [J].
ARMSTRONG, FA ;
BOND, AM ;
HILL, HAO ;
PSALTI, ISM ;
ZOSKI, CG .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (17) :6485-6493
[8]   METAL-IONS AND COMPLEXES AS MODULATORS OF PROTEIN INTERFACIAL ELECTRON-TRANSPORT AT GRAPHITE-ELECTRODES [J].
ARMSTRONG, FA ;
COX, PA ;
HILL, HAO ;
LOWE, VJ ;
OLIVER, BN .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 217 (02) :331-366
[10]   DIRECT ELECTROCHEMISTRY OF REDOX PROTEINS AT PYROLYTIC-GRAPHITE ELECTRODES [J].
ARMSTRONG, FA ;
HILL, HAO ;
OLIVER, BN ;
WALTON, NJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (04) :921-923