Electrochemiluminescent/voltammetric toxicity screening sensor using enzyme-generated DNA damage

被引:38
作者
So, Minjeong
Hvastkovs, Eli G.
Schenkman, John B.
Rusling, James F.
机构
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Univ Connecticut, Ctr Hlth, Dept Pharmacol, Farmington, CT 06032 USA
关键词
biosensor; Genotoxicity; enzyme bioactivation; DNA damage; electrochemiluminescence; square wave voltammetry;
D O I
10.1016/j.bios.2007.06.017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Simultaneous optical and voltammetric detection of bioactivated genotoxicity is reported for the first time employing ultrathin films of DNA, model metabolic enzymes, and electrochemiluminescence (ECL) generating metallopolymer [Ru(bpy)(2)PVP10](2+) on pyrolytic graphite (PG) electrodes. Cytochrome P450(cam) and myoglobin were used as model monoxygenase enzymes to mimic in vivo processes. Sensor film growth and component amounts were monitored using a quartz crystal microbalance (QCM). Subsequent to the enzyme reaction, DNA damage in the sensor films was measured simultaneously using a simple apparatus combining a standard voltammetry cell coupled with an optical fiber and photomultiplier tube. The model enzyme reaction converted styrene to styrene oxide, which reacts with DNA nucleobases. ECL and SWV signals increased with enzyme reaction time on the scale of several min, and provided relative enzyme turnover rates for DNA damage suitable for toxicity screening applications. Within 1 min, the sensor detects similar to 3 damaged bases per 10,000 DNA bases using this simultaneous detection. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:492 / 498
页数:7
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