Chernogolov A A, Usanov S A
Institute of Bioorganic Chemistry, Academy of Sciences of Belarus, Minsk, Belarus.
Biochemistry (Mosc). 1997 Dec;62(12):1375-84.
The effects of antibodies against protein components of the monooxygenase systems of adrenocortical mitochondria on the reactions of hydroxylation of cholesterol and 11 beta-deoxycorticosterone were investigated in a reconstituted system containing cytochromes P450scc (CYP11A1) and P450(11 beta) (CYP11B1) as the terminal oxidases and the electron-transfer proteins adrenodoxin reductase and adrenodoxin. It has been shown that affinity-purified antibodies to cytochromes P450scc and P450(11) beta are efficient modulators of the activity of these systems, and their inhibiting effect is mainly due to interference with the interaction of heme proteins and adrenodoxin. The antibodies against polypeptide fragments of the cytochrome P450scc molecule F1 (Ile1-Arg256), F2 (Asn257-Ala481), and F3 (Asn257-Arg399) were used to demonstrate that the interaction of heme protein with adrenodoxin has a multisite character and involves regions located in the N- and C-terminal sequences of cytochrome P450scc.
在一个重组系统中,研究了针对肾上腺皮质线粒体单加氧酶系统蛋白质成分的抗体对胆固醇和11β-脱氧皮质酮羟基化反应的影响。该重组系统包含细胞色素P450scc(CYP11A1)和P450(11β)(CYP11B1)作为末端氧化酶以及电子传递蛋白肾上腺皮质铁氧还蛋白还原酶和肾上腺皮质铁氧还蛋白。结果表明,针对细胞色素P450scc和P450(11)β的亲和纯化抗体是这些系统活性的有效调节剂,其抑制作用主要是由于干扰了血红素蛋白与肾上腺皮质铁氧还蛋白的相互作用。利用针对细胞色素P450scc分子F1(Ile1-Arg256)、F2(Asn257-Ala481)和F3(Asn257-Arg399)多肽片段的抗体,证明了血红素蛋白与肾上腺皮质铁氧还蛋白的相互作用具有多位点特征,且涉及细胞色素P450scc N端和C端序列中的区域。