Mechanism of Intermolecular Interactions of Microsomal Cytochrome P450s CYP17 and CYP21 Involved in Steroid Hormone Biosynthesis

被引：16

作者：

Sushko, T. A. ^{[1
]}

Gilep, A. A. ^{[1
]}

Usanov, S. A. ^{[1
]}

机构：

[1] Natl Acad Sci Belarus, Inst Bioorgan Chem, Minsk 220141, BELARUS

来源：

BIOCHEMISTRY-MOSCOW | 2012年 / 77卷 / 06期

关键词：

cytochrome P450; CYP17; CYP21; protein-protein interaction; steroid hormone biosynthesis; REDOX PARTNERS; REDUCTASE; EXPRESSION; BINDING; PURIFICATION; STEROIDOGENESIS; OXIDOREDUCTASE; IDENTIFICATION; HYDROXYLASE; ENZYMES;

D O I：

10.1134/S0006297912060041

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Protein-protein interactions play a significant role in regulation of functional activity of cytochrome P450s. The aim of the present study was to elucidate the molecular interactions between steroidogenic enzymes CYP17 and CYP21 localized in endoplasmic reticulum membranes of adrenal cortex and involved in biosynthesis of corticosteroid hormones. In the present work, we demonstrate for the first time the direct interaction at molecular level between highly purified human recombinant cytochrome P450s in a mixed reconstituted system. The dependence of the interaction between CYP17 and CYP21 on concentration of the redox-partner - NADPH-cytochrome P450 reductase - is demonstrated, and it is shown that electrostatic interactions play a crucial role in the interaction between CYP17 and CYP21.

引用

页码：585 / 592

页数：8

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