Voorman R, Aust S D
Department of Biochemistry, Michigan State University, East Lansing 48824.
J Biochem Toxicol. 1989 Summer;4(2):105-9. doi: 10.1002/jbt.2570040206.
Based on data indicating that compounds which induce cytochrome P-450d also bind to the enzyme [R. Voorman and S. D. Aust (1987). Toxicol. Appl. Pharmacol. 90, 69-78], we investigated the inhibition of cytochrome P-450d-dependent estradiol 2-hydroxylase by (2,3,7,8-tetrachlorodibenzo-p-dioxin TCDD), using ligand-free cytochrome P-450d from isosafrole-treated rats. Since maximum inhibition of estradiol 2-hydroxylase occurred at TCDD concentrations comparable to the concentration of enzyme (50 nM), a modified form of steady-state kinetic analysis was used. Using I50 = Et/2 + Ki where Et = total enzyme concentration), we showed that TCDD inhibited cytochrome P-450d-dependent estradiol 2-hydroxylase activity with Ki equal to 8 nM. Association of TCDD with P-450d occurred within 2 min of inhibitor addition. Therefore, TCDD can be considered a tight binding inhibitor of cytochrome P-450d.
基于数据表明,诱导细胞色素P - 450d的化合物也与该酶结合[R. 沃尔曼和S. D. 奥斯特(1987年)。毒理学与应用药理学。90,69 - 78],我们使用来自异黄樟素处理大鼠的无配体细胞色素P - 450d,研究了(2,3,7,8 - 四氯二苯并 - p - 二恶英,TCDD)对细胞色素P - 450d依赖性雌二醇2 - 羟化酶的抑制作用。由于在与酶浓度(50 nM)相当的TCDD浓度下,雌二醇2 - 羟化酶出现最大抑制,因此使用了一种改良形式的稳态动力学分析。使用I50 = Et/2 + Ki(其中Et = 总酶浓度),我们表明TCDD抑制细胞色素P - 450d依赖性雌二醇2 - 羟化酶活性,Ki等于8 nM。TCDD与P - 450d的结合在加入抑制剂后2分钟内发生。因此,TCDD可被视为细胞色素P - 450d的紧密结合抑制剂。