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Evaluating enzymes that generate genotoxic benzo[a]pyrene metabolites using sensor arrays

机译:使用传感器阵列评估产生遗传毒性苯并[a]]代谢物的酶

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摘要

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.
机译:评估了具有分别可寻址,可拆卸电极的极薄DNA /酶膜涂层电极的阵列,以评估几种不同酶同时对苯并[a] re(BP)进行遗传毒性生物活化的相对速率。具体来说,阵列中的细胞色素(cyt)P450cam,cyt P40 1A2和肌红蛋白被H2O2激活,以将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对DNA的损害。 Cyt P450cam和cyt P450 1A2的BP遗传毒性生物活化活性比肌红蛋白高3倍。阵列同时产生和检测几种酶的基于代谢物的DNA损伤的能力是一种快速且有前途的方法,可用于鉴定和表征与药物和污染物的遗传毒性有关的酶。

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