Papadopoulos Vassilios, Liu Jun, Culty Martine
Department of Biochemistry & Molecular and Cellular Biology, Georgetown University Medical Center, 3900 Reservoir Road, NW, Washington, DC 20057, USA.
Mol Cell Endocrinol. 2007 Feb;265-266:59-64. doi: 10.1016/j.mce.2006.12.004. Epub 2007 Feb 5.
Cholesterol transport into mitochondria is the rate-determining and hormone-sensitive step in steroid biosynthesis. During the last few years two proteins were shown to be critical for this process: the mitochondrial translocator protein, previously known as peripheral-type benzodiazepine receptor, and the steroidogenic acute regulatory protein. In this manuscript we review evidence suggesting that these two proteins functionally interact to facilitate cholesterol transport and may be part of a larger multimeric mitochondrial complex of proteins assembled to facilitate the hormone-induced cholesterol transfer into mitochondria. This complex might include proteins such as the mitochondrial voltage-dependent anion channel, the translocator protein-associated protein PAP7 which also functions as an A kinase anchor protein that binds and brings into the complex the regulatory subunit Ialpha of the cAMP-dependent protein kinase.
胆固醇转运至线粒体是类固醇生物合成中决定速率且受激素调节的步骤。在过去几年中,有两种蛋白质被证明对这一过程至关重要:线粒体转位蛋白(以前称为外周型苯二氮䓬受体)和类固醇生成急性调节蛋白。在本论文中,我们综述了相关证据,表明这两种蛋白质在功能上相互作用以促进胆固醇转运,并且可能是一个更大的线粒体多聚体蛋白复合物的一部分,该复合物组装起来以促进激素诱导的胆固醇转运至线粒体。这个复合物可能包括诸如线粒体电压依赖性阴离子通道、转位蛋白相关蛋白PAP7等蛋白质,PAP7还作为一种A激酶锚定蛋白发挥作用,它结合并将环磷酸腺苷依赖性蛋白激酶的调节亚基Iα带入复合物中。