Ogishima T, Okada Y, Omura T
J Biochem. 1985 Sep;98(3):781-91. doi: 10.1093/oxfordjournals.jbchem.a135335.
Isolated bovine adrenal cortex mitochondria imported in vitro synthesized pre-P-450(SCC) and processed it to the mature form. Partial radio-sequencing of the processed P-450(SCC) gave a result identical with that for authentic P-450(SCC). Rat liver mitochondria also imported pre-P-450(SCC) and processed it to the mature form, whereas bovine heart mitochondria were unable to import and process pre-P-450(SCC) although both mitochondrial preparations imported and processed pre-adrenodoxin. The pre-P-450(SCC) processing activity of bovine adrenal cortex mitochondria was associated with the matrix side surface of the inner membrane. The processing protease could be solubilized by sodium cholate and partially purified by ammonium sulfate fractionation. The partially purified processing protease cleaved pre-P-450(SCC) at the correct position. It was also active in processing pre-P-450(11 beta) but inactive toward pre-adrenodoxin. Bovine heart mitochondria lacked the processing activity to pre-P-450(SCC). The localization of pre-P-450(SCC) and mature P-450(SCC) in bovine adrenal cortex mitochondria was examined. Mature P-450(SCC) processed by the mitochondria was found associated with the matrix-side surface of the inner membrane, which is the correct location of P-450(SCC) in the cell. In the presence of o-phenanthroline, pre-P-450(SCC) was imported into the organelles without being processed and remained soluble in the matrix. The incorporation of newly processed mature P-450(SCC) into the inner membrane was also observed when pre-P-450(SCC) was incubated with inner membrane vesicles. Mature P-450(SCC) generated in vitro from pre-P-450(SCC) by the partially purified processing protease was incorporated not only into the inner membrane vesicles but also into bovine adrenal cortex microsomes. These findings suggested that the processing of pre-P-450(SCC) occurred prior to the incorporation of mature-P-450(SCC) into the inner membrane.
体外导入的分离牛肾上腺皮质线粒体可导入体外合成的前P - 450(SCC)并将其加工成成熟形式。对加工后的P - 450(SCC)进行部分放射性测序,结果与天然P - 450(SCC)相同。大鼠肝线粒体也能导入前P - 450(SCC)并将其加工成成熟形式,而牛心肌线粒体虽然两种线粒体制剂都能导入并加工前肾上腺皮质铁氧化还原蛋白,但却无法导入和加工前P - 450(SCC)。牛肾上腺皮质线粒体的前P - 450(SCC)加工活性与内膜的基质侧表面相关。加工蛋白酶可用胆酸钠溶解,并通过硫酸铵分级分离进行部分纯化。部分纯化的加工蛋白酶在正确位置切割前P - 450(SCC)。它在加工前P - 450(11β)时也有活性,但对前肾上腺皮质铁氧化还原蛋白无活性。牛心肌线粒体缺乏对前P - 450(SCC)的加工活性。研究了前P - 450(SCC)和成熟P - 450(SCC)在牛肾上腺皮质线粒体中的定位。发现由线粒体加工的成熟P - 450(SCC)与内膜的基质侧表面相关,这是P - 450(SCC)在细胞中的正确位置。在邻菲罗啉存在的情况下,前P - 450(SCC)被导入细胞器但未被加工,并仍可溶于基质中。当前P - 450(SCC)与内膜囊泡一起孵育时,也观察到新加工的成熟P - 450(SCC)掺入内膜。由部分纯化的加工蛋白酶从前P - 450(SCC)体外生成的成熟P - 450(SCC)不仅掺入内膜囊泡,还掺入牛肾上腺皮质微粒体。这些发现表明,前P - 450(SCC)的加工发生在成熟P - 450(SCC)掺入内膜之前。