Steroidogenic Acute Regulatory Protein: Structure, Functioning, and Regulation

被引:34
|
作者
Tugaeva, K. V. [1 ,2 ]
Sluchanko, N. N. [1 ,3 ]
机构
[1] Russian Acad Sci, Bach Inst Biochem, Fed Res Ctr Biotechnol, Moscow 119071, Russia
[2] Lomonosov Moscow State Univ, Biol Fac, Dept Biochem, Moscow 119234, Russia
[3] Lomonosov Moscow State Univ, Biol Fac, Dept Biophys, Moscow 119991, Russia
基金
俄罗斯科学基金会; 俄罗斯基础研究基金会;
关键词
cholesterol; lipid-binding proteins; protein structure; protein-protein interactions; steroidogenesis; phosphorylation; steroids; PHOSPHATIDYLCHOLINE TRANSFER PROTEIN; INDUCED MITOCHONDRIAL PROTEIN; 14-3-3-GAMMA ADAPTER PROTEIN; TISSUE-SPECIFIC EXPRESSION; LIPID-TRANSFER PROTEINS; MEMBRANE CONTACT SITES; STEROL CARRIER PROTEIN; SIDE-CHAIN CLEAVAGE; STAR PROTEIN; BENZODIAZEPINE-RECEPTOR;
D O I
10.1134/S0006297919140141
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
Steroidogenesis takes place mainly in adrenal and gonadal cells that produce a variety of structurally similar hormones regulating numerous body functions. The rate-limiting stage of steroidogenesis is cholesterol delivery to the inner mitochondrial membrane, where it is converted by cytochrome P450scc into pregnenolone, a common precursor of all steroid hormones. The major role of supplying mitochondria with cholesterol belongs to steroidogenic acute regulatory protein (STARD1). STARD1, which is synthesized de novo as a precursor containing mitochondrial localization sequence and sterol-binding domain, significantly accelerates cholesterol transport and production of pregnenolone. Despite a tremendous interest in STARD1 fueled by its involvement in hereditary diseases and extensive efforts of numerous laboratories worldwide, many aspects of STARD1 structure, functioning, and regulation remain obscure and debatable. This review presents current concepts on the structure of STARD1 and other lipid transfer proteins, the role of STARD1 in steroidogenesis, and the mechanism of its functioning, as well as identifies the most controversial and least studied questions related to the activity of this protein.
引用
收藏
页码:233 / 253
页数:21
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