Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
Methods Enzymol. 2023;689:39-63. doi: 10.1016/bs.mie.2023.04.001. Epub 2023 Apr 25.
Cytochrome P450 (P450) 17A1 plays a key role in steroidogenesis, in that this enzyme catalyzes the 17α-hydroxylation of both pregnenolone and progesterone, followed by a lyase reaction to cleave the C-20 land C-21 carbons from each steroid. The reactions are important in the production of both glucocorticoids and androgens. The enzyme is critical in humans but is also a drug target in treatment of prostate cancer. Detailed methods are described for the heterologous expression of human P450 17A1 in bacteria, purification of the recombinant enzyme, reconstitution of the enzyme system in the presence of cytochrome b, and chromatographic procedures for sensitive analyses of reaction products. Historic assay approaches are reviewed. Some information is also provided about outstanding questions in the research field, including catalytic mechanisms and searches for selective inhibitors.
细胞色素 P450(P450)17A1 在类固醇生成中起着关键作用,因为这种酶催化 pregnenolone 和 progesterone 的 17α-羟化作用,然后进行裂解反应,从每种类固醇中裂解 C-20 和 C-21 碳。这些反应对于糖皮质激素和雄激素的产生都很重要。该酶在人类中至关重要,但也是治疗前列腺癌的药物靶点。本文详细描述了在细菌中异源表达人 P450 17A1、纯化重组酶、在细胞色素 b 存在下重建酶系统以及用于敏感分析反应产物的色谱程序。还回顾了历史检测方法。还提供了有关该研究领域悬而未决的问题的一些信息,包括催化机制和选择性抑制剂的寻找。