Krainev A G, Weiner L M, Alferyev I S, Mikhalin N V
Institute of Chemical Kinetics and Combustion, Novosibirsk, U.S.S.R.
Biochem Biophys Res Commun. 1988 Jan 15;150(1):426-35. doi: 10.1016/0006-291x(88)90538-4.
To solve the problem of localization of the active center of cytochrome P-450 in microsomal membranes, new bifunctional compounds (I-IV), which contain pyridine radical, aliphatic chain of variable length and diphosphonic acid ("floating" molecules) have been applied. These compounds inhibit oxidation and binding of the substrates of cytochrome P-450 (aminopyrine and aniline), inhibition being of a competitive character. Measurements of distribution coefficients between water and membranes of microsomes and liposomes from egg phosphatidylcholine evidence that the microsomal proteins are necessary for providing effective interaction of I-IV with microsomal membrane. The 1H-NMR method has demonstrated compounds to be incorporated into lipid bilayer so that the non-polar part is in the inner membrane volume. The results obtained confirm our previous conclusion (Krainev A.G., Weiner L.M., Alferyev I.S., Slynko N.M. (1985) Biochim. Biophys. Acta, 818, 96-104) about localization of the active center of microsomal cytochrome P-450 at the depth of approximately 18 A from the hydrophilic surface of a membrane.
为了解决细胞色素P - 450活性中心在微粒体膜中的定位问题,已应用了新型双功能化合物(I - IV),这些化合物含有吡啶基、可变长度的脂肪链和二膦酸(“浮动”分子)。这些化合物抑制细胞色素P - 450底物(氨基比林和苯胺)的氧化和结合,抑制作用具有竞争性。对来自鸡蛋磷脂酰胆碱的微粒体和脂质体的水与膜之间分配系数的测量表明,微粒体蛋白对于I - IV与微粒体膜的有效相互作用是必需的。1H - NMR方法已证明化合物被纳入脂质双层,使得非极性部分位于内膜体积中。所获得的结果证实了我们先前的结论(Krainev A.G., Weiner L.M., Alferyev I.S., Slynko N.M.(1985年)Biochim. Biophys. Acta,818,96 - 104),即微粒体细胞色素P - 450的活性中心位于距膜亲水表面约18埃深处。