Horie S, Ishii H, Nakazawa H, Suga T, Orii H
Biochim Biophys Acta. 1979 Jul 4;585(3):435-43. doi: 10.1016/0304-4165(79)90088-6.
The cross-points of rat liver peroxisomes, peroxisomal core and the core components were determined by means of cross-partition in two phase systems. The partitions were carried out in the systems containing 6% (w/w) Dextran T 500 and 6% (w/w) polyethyleneglycol 4000 in sodium salts. The same cross-point, pH 5.6, was obtained in peroxisomal marker enzymes in light mitochondrial fraction of liver homogenate, such as catalase, D-amino acid oxidase and urate oxidase. The cross-point as determined by cross-partition of purified peroxisomal core was 6.7. The cross-points of urate oxidase and framework protein fractions obtained by alkali treatment on the purified core were 7.8 and 4.2, respectively, and the ratio of the proteins of urate oxidase to framework protein was 2 : 1. The theoretical value of cross-point of the core calculated from from the relationship between the cross-point and protein ratio of each component of the core coincided with the experimental value obtained by this method.
通过两相系统中的交叉分配法确定大鼠肝脏过氧化物酶体、过氧化物酶体核心及核心组分的交叉点。分配在含有6%(w/w)葡聚糖T 500和6%(w/w)聚乙二醇4000钠盐的系统中进行。在肝脏匀浆轻线粒体部分的过氧化物酶体标记酶中,如过氧化氢酶、D-氨基酸氧化酶和尿酸氧化酶,获得了相同的交叉点pH 5.6。纯化的过氧化物酶体核心交叉分配法测定的交叉点为6.7。纯化核心经碱处理得到的尿酸氧化酶和骨架蛋白组分的交叉点分别为7.8和4.2,尿酸氧化酶与骨架蛋白的蛋白质比例为2:1。根据核心各组分的交叉点与蛋白质比例之间的关系计算出的核心交叉点理论值与该方法获得的实验值相符。