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Steroid 17α-hydroxylase/17, 20-lyase (cytochrome P450 17A1).
Guengerich, F Peter; McCarty, Kevin D; Tateishi, Yasuhiro; Liu, Lu.
Afiliação
  • Guengerich FP; Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States. Electronic address: f.guengerich@vanderbilt.edu.
  • McCarty KD; Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
  • Tateishi Y; Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
  • Liu L; Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
Methods Enzymol ; 689: 39-63, 2023.
Article em En | MEDLINE | ID: mdl-37802581
ABSTRACT
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 b5, 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Liases Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Liases Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article