Voltammetry of immobilized cytochrome c on novel binary self-assembled monolayers of thioctic acid and thioctic amide modified gold electrodes

被引:23
作者
Ji, Xueping
Jin, Baokang
Jin, Jiye
Nakamura, Toshio
机构
[1] Shinshu Univ, Fac Sci, Dept Chem, Matsumoto, Nagano 3908621, Japan
[2] Anhui Univ, Dept Chem, Hefei 230039, Anhui, Peoples R China
关键词
self-assembled monolayer; cyclic voltammetry; cytochrome c; gold electrode;
D O I
10.1016/j.jelechem.2006.03.011
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Horse heart cytochrome c (cyt c) was adsorbed on the binary self-assembled monolayers (SAMs) composed of thioctic acid (T-COOH) and thioctic amide (T-NH2) at gold electrodes via electrostatic interaction. The cyt c adsorbed on the modified gold electrode exhibited well-defined reversible electrochemical behavior in 10 mM phosphate buffer solution (PBS, pH 7.0). The surface concentration (F) of electroactive species, cyt c, on the binary SAMs was higher than that in single-component SAMs of T-COOH, and reached a maximum value of 9.2 x 10(-12) mol cm(-2) when the ratio of T-COOH to T-NH2 in adsorption solution was of 3:2, and the formal potential (E-0' = (E-pa + E-pc)/2) of cyt c was -0.032 V (vs. Ag vertical bar AgCl (3 M NaCl)) in a 10 mM PBS. The interaction between cyt c and the binary SAMs made the E-0' shift negatively when compared with that of cyt c in solution (+0.258 V vs. NHE, i.e., +0.058 V vs. Ag vertical bar AgCl (3 M NaCl)). The fractional coverage of bound cyt c was a 0.64 theoretical monolayer. The standard electron transfer rate constant of cyt c immobilized on the binary SAMs was also higher than that on single-component SAMs of T-COOH, and the maximum value of 15.8 +/- 0.6 s(-1) was obtained when the ratio of T-COOH to T-NH2 in adsorption solution was at 3:2. The results suggest that the electrode modified with the binary SAMs functions better than the electrode modified with single-component SAMs of T-COOH. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 180
页数:8
相关论文
共 47 条
[11]   VOLTAMMETRY OF COVALENTLY IMMOBILIZED CYTOCHROME-C ON SELF-ASSEMBLED MONOLAYER ELECTRODES [J].
COLLINSON, M ;
BOWDEN, EF ;
TARLOV, MJ .
LANGMUIR, 1992, 8 (05) :1247-1250
[12]   Formation and electrochemical characterization of self-assembled monolayers of thioctic acid on polycrystalline gold electrodes in phosphate buffer pH 7.4 [J].
Dijksma, M ;
Kamp, B ;
Hoogvliet, JC ;
van Bennekom, WP .
LANGMUIR, 2000, 16 (08) :3852-3857
[13]   Effect of hexacyanoferrate(II/III) on self-assembled monolayers of thioctic acid and 11-mercaptoundecanoic acid on gold [J].
Dijksma, M ;
Boukamp, BA ;
Kamp, B ;
van Bennekom, WP .
LANGMUIR, 2002, 18 (08) :3105-3112
[14]   OXIDATION-REDUCTION POTENTIALS OF CYTOCHROMES IN MITOCHONDRIA [J].
DUTTON, PL ;
WILSON, DF ;
LEE, CP .
BIOCHEMISTRY, 1970, 9 (26) :5077-&
[15]  
EDDOWES MJ, 1977, J CHEM SOC CHEM COMM, P771
[16]   Controlling interfacial electron-transfer kinetics of cytochrome c with mixed self-assembled monolayers [J].
El Kasmi, A ;
Wallace, JM ;
Bowden, EF ;
Binet, SM ;
Linderman, RJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (01) :225-226
[17]   Redox reactions of heme-containing metalloproteins:: dynamic effects of self-assembled monolayers on thermodynamics and kinetics of cytochrome c electron-transfer reactions [J].
Fedurco, M .
COORDINATION CHEMISTRY REVIEWS, 2000, 209 :263-331
[18]   ELECTROREFLECTANCE SPECTROSCOPIC STUDY OF THE ELECTRON-TRANSFER RATE OF CYTOCHROME-C ELECTROSTATICALLY IMMOBILIZED ON THE OMEGA-CARBOXYL ALKANETHIOL MONOLAYER MODIFIED GOLD ELECTRODE [J].
FENG, ZQ ;
IMABAYASHI, S ;
KAKIUCHI, T ;
NIKI, K .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 394 (1-2) :149-154
[19]   PHASE-BEHAVIOR OF 2-COMPONENT SELF-ASSEMBLED MONOLAYERS OF ALKANETHIOLATES ON GOLD [J].
FOLKERS, JP ;
LAIBINIS, PE ;
WHITESIDES, GM ;
DEUTCH, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (02) :563-571
[20]   Direct electron transfer between heme-containing enzymes and electrodes as basis for third generation biosensors [J].
Gorton, L ;
Lindgren, A ;
Larsson, T ;
Munteanu, FD ;
Ruzgas, T ;
Gazaryan, I .
ANALYTICA CHIMICA ACTA, 1999, 400 :91-108