Direct electrochemistry and electrocatalysis of hemoglobin on chitosan-room temperature ionic liquid-TiO2-graphene nanocomposite film modified electrode

被引:100
作者
Sun, Jun-Yong [1 ]
Huang, Ke-Jing [1 ]
Zhao, Su-Fang [1 ]
Fan, Yang [1 ]
Wu, Zhi-Wei [1 ]
机构
[1] Xinyang Normal Univ, Coll Chem & Chem Engn, Xinyang 464000, Peoples R China
基金
中国国家自然科学基金;
关键词
Hemoglobin; Direct electrochemistry; TiO2-graphene nanocomposite; Ionic liquid; Hydrogen peroxide; BY-LAYER FILMS; HEME-PROTEINS; PHOSPHATIDYLCHOLINE FILMS; NANOSTRUCTURED TIO2; HYDROGEN-PEROXIDE; CARBON; GRAPHENE; BIOSENSOR; NANOTUBES; MYOGLOBIN;
D O I
10.1016/j.bioelechem.2011.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TiO2-graphene nanocomposite was prepared by hydrolysis of titanium isopropoxide in colloidal suspension of graphene oxide and in situ hydrothermal treatment. The direct electrochemistry and electrocatalysis of hemoglobin in room temperature ionic liquid 1-Butyl-3-methylimidazolium hexafluorophosphate, chitosan and TiO2-graphene nanocomposite modified glassy carbon electrode were investigated. The biosensor was examined by using UV-vis spectroscopy, scanning electron microscopy and electrochemical methods. The results indicated that hemoglobin remained its bioactivity on the modified electrode, showing a couple of well-defined and quasi-reversible redox peaks, corresponding to hemoglobin Fe-III/Fe-II couple. The kinetic parameters for the electrode reaction, such as the formal potential (E-o), the electron transfer rate constant (k(s)), the apparent coverage (Gamma). and Michaelis-Menten constant (K-m) were evaluated. The biosensor showed good electrochemical responses to the reduction of H2O2 in the ranges of 1-1170 mu M. The detection limit was 0.3 mu M (S/N=3). The properties of this composite film, together with the bioelectrochemical catalytic activity, could make them useful in the development of bioelectronic devices, and investigation of electrochemistry of other heme proteins at functional interface. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 57 条
[1]   Electrodeposition of monodispersed Fe nanocrystals from an ionic liquid [J].
Aravinda, CL ;
Freyland, W .
CHEMICAL COMMUNICATIONS, 2004, (23) :2754-2755
[2]   Recent developments in faradaic bioelectrochemistry [J].
Armstrong, FA ;
Wilson, GS .
ELECTROCHIMICA ACTA, 2000, 45 (15-16) :2623-2645
[3]   New nanostructured TiO2 for direct electrochemistry and glucose sensor applications [J].
Bao, Shu-Juan ;
Li, Chang Ming ;
Zang, Jian-Feng ;
Cui, Xiao-Qiang ;
Qiao, Yan ;
Guo, Jun .
ADVANCED FUNCTIONAL MATERIALS, 2008, 18 (04) :591-599
[4]  
Bard AJ, 1980, ELECTROCHEMICAL METH, P258
[5]   Graphene-based materials in electrochemistry [J].
Chen, Da ;
Tang, Longhua ;
Li, Jinghong .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (08) :3157-3180
[6]   Ionic liquid (molten salt) phase organometallic catalysis [J].
Dupont, J ;
de Souza, RF ;
Suarez, PAZ .
CHEMICAL REVIEWS, 2002, 102 (10) :3667-3691
[7]   Electropolymerization of benzene in a room temperature ionic liquid [J].
El Abedin, SZ ;
Borissenko, N ;
Endres, F .
ELECTROCHEMISTRY COMMUNICATIONS, 2004, 6 (04) :422-426
[8]   Direct electron transfer and electrocatalysis of hemoglobin adsorbed on mesoporous carbon through layer-by-layer assembly [J].
Feng, Jiu-Ju ;
Xu, Jing-Juan ;
Chen, Hong-Yuan .
BIOSENSORS & BIOELECTRONICS, 2007, 22 (08) :1618-1624
[9]   Direct electron transfer and electrocatalysis of hemoglobin adsorbed onto electrodeposited mesoporous tungsten oxide [J].
Feng, JJ ;
Xu, JJ ;
Chen, HY .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (01) :77-82
[10]   Protein engineering using molecular assembly: Functional conversion of cytochrome c via noncovalent interactions [J].
Hamachi, I ;
Fujita, A ;
Kunitake, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (39) :9096-9102