Wang Bingquan, Jansson Ingela, Schenkman John B, Rusling James F
Department of Chemistry, University of Connecticut, U-60, 55 North Eagleville Road, Storrs, Connecticut 06269-3060, USA.
Anal Chem. 2005 Mar 1;77(5):1361-7. doi: 10.1021/ac0485536.
Arrays with individually addressable, demountable electrodes coated with ultrathin DNA/enzyme films were evaluated to estimate relative rates of genotoxic bioactivation of benzo[a]pyrene (BP) for several different enzymes simultaneously. Specifically, cytochrome (cyt) P450cam, cyt P40 1A2, and myoglobin in the array were activated with H2O2 to metabolize BP to genotoxic metabolites. DNA damage by the metabolites was detected by increases in square wave voltammetric oxidation peaks using Ru(bpy)3(2+) as catalyst. Cyt P450cam and cyt P450 1A2 showed 3-fold higher activity for genotoxic bioactivation of BP than myoglobin. The ability of the arrays to generate and detect metabolite-based DNA damage simultaneously for several enzymes is a rapid and promising approach to identify and characterize enzymes involved in genotoxicity of drugs and pollutants.
对带有可单独寻址、可拆卸电极且涂覆有超薄DNA/酶膜的阵列进行了评估,以同时估计几种不同酶对苯并[a]芘(BP)的遗传毒性生物活化相对速率。具体而言,阵列中的细胞色素(cyt)P450cam、cyt P450 1A2和肌红蛋白用H2O2激活,将BP代谢为遗传毒性代谢物。使用Ru(bpy)3(2+)作为催化剂,通过方波伏安氧化峰的增加来检测代谢物引起的DNA损伤。Cyt P450cam和cyt P450 1A2对BP的遗传毒性生物活化活性比肌红蛋白高3倍。该阵列能够同时为几种酶生成并检测基于代谢物的DNA损伤,是一种快速且有前景的方法,可用于识别和表征参与药物和污染物遗传毒性的酶。