Hemrika W, Berden J A
E.C. Slater Institute for Biochemical Research, University of Amsterdam, The Netherlands.
Eur J Biochem. 1990 Sep 24;192(3):761-5. doi: 10.1111/j.1432-1033.1990.tb19287.x.
The topology of the subunits of ubiquinol-cytochrome-c oxidoreductase of the yeast Saccharomyces cerevisiae has been determined using a digitonin/proteinase K assay. With this assay we were able selectively to disrupt the mitochondrial membranes and to identify the subunits which became proteinase-K sensitive after disruption of either the outer or both outer and inner membranes. This approach confirmed previous indications for the localization of the core I protein, cytochrome c1, cytochrome b, the FeS protein and the 17-kDa subunit, while it also provided direct evidence for the site of accessibility to proteinase K of the 14-kDa and 11-kDa subunits. The 14-kDa subunit faces the mitochondrial matrix and the 11-kDa subunit faces the intermembrane space.
利用洋地黄皂苷/蛋白酶K分析法确定了酿酒酵母泛醇-细胞色素c氧化还原酶亚基的拓扑结构。通过该分析法,我们能够选择性地破坏线粒体膜,并鉴定出在破坏外膜或同时破坏外膜和内膜后对蛋白酶K敏感的亚基。这种方法证实了之前关于核心I蛋白、细胞色素c1、细胞色素b、铁硫蛋白和17 kDa亚基定位的指示,同时也为14 kDa和11 kDa亚基对蛋白酶K的可及位点提供了直接证据。14 kDa亚基面向线粒体基质,11 kDa亚基面向膜间隙。