Covalent immobilization of horseradish peroxidase via click chemistry and its direct electrochemistry

被引:22
作者
Ran, Qin [1 ]
Peng, Ru [1 ]
Liang, Cong [1 ]
Ye, Siqiu [1 ]
Xian, Yuezhong [1 ]
Zhang, Wenjing [1 ]
Jin, Litong [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai 20062, Peoples R China
基金
中国国家自然科学基金;
关键词
Direct electrochemistry; Horseradish peroxidase; Click chemistry; Biosensor; DIRECT ELECTRON-TRANSFER; SURFACE-ENHANCED RAMAN; GOLD NANOPARTICLES; HYDROGEN-PEROXIDE; CYTOCHROME-C; ENZYMATIC-ACTIVITY; REDOX ENZYMES; FILM; HEMOGLOBIN; ELECTRODEPOSITION;
D O I
10.1016/j.talanta.2010.11.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple and versatile approach for covalent immobilization of redox protein on solid surface via self-assembled technique and click chemistry is reported. The alkynyl-terminated monolayers are obtained by self-assembled technique, then, azido-horseradish peroxidase (azido-HRP) was covalent immobilized onto the formed monolayers by click reaction. The modified process is characterized by reflection absorption infrared spectroscopy (RAIR), surface-enhanced Raman scattering spectroscopy (SERS) and electrochemical methods. All the experimental results suggest that HRP is immobilized onto the electrode surface successfully without denaturation. Furthermore, the immobilized HRP shows electrocatalytic reduction for H2O2, and the linear range is from 5.0 to 700 mu M. The heterogeneous electron transfer rate constant k(s) is 1.11 s(-1) and the apparent Michaelis-Menten constant is calculated to be 0.196 mM. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1381 / 1385
页数:5
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