Yang C S, Strickhart F S, Kicha L P
Biochim Biophys Acta. 1978 May 18;509(2):326-37. doi: 10.1016/0005-2736(78)90051-2.
Solubilized NADPH-cytochrome P-450 reductase has been purified from liver microsomes of phenobarbital-treated rats. When added to microsomes, the reductase enhances the monoxygenase, such as aryl hydrocarbon hydroxylase, ethoxycoumarin O-dealkylase, and benzphetamine N-demethylase, activities. The enhancement can be observed with microsomes prepared from phenobarbital- or 3-methylcholanthrene-treated, or non-treated rats. The added reductase is believed to be incorporated into the microsomal membrane, and the rate of the incorporation can be assayed by measuring the enhancement in ethoxycoumarin dealkylase activity. It requires a 30 min incubation at 37 degrees C for maximal incorporation and the process is much slower at lower temperatures. The temperature affects the rate but not the extent of the incorporation. After the incorporation, the enriched microsomes can be separated from the unbound reductase by gel filtration with a Sepharose 4B column. The relationship among the reductase added, reductase bound and the enhancement in hydroxylase activity has been examined. The relationship between the reductase level and the aryl hydrocarbon hydroxylase activity has also been studied with trypsin-treated microsomes. The trypsin treatment removes the reductase from the microsomes, and the decrease in reductase activity is accompanied by a parallel decrease in aryl hydrocarbon hydroxylase activity. When purified reductase is added, the treated microsomes are able to gain aryl hydrocarbon hydroxylase activity to a level comparable to that which can be obtained with normal microsomes. The present study demonstrates that purified NADPH-cytochrome P-450 reductase can be incorporated into the microsomal membrane and the incorporated reductase can interact with the cytochrome P-450 molecules in the membrane, possibly in the same mode as the endogenous reductase molecules. The result is consistent with a non-rigid model for the organization of cytochrome P-450 and NADPH-cytochrome P-450 reductase in the microsomal membrane.
已从苯巴比妥处理的大鼠肝脏微粒体中纯化出可溶的NADPH - 细胞色素P - 450还原酶。当将该还原酶添加到微粒体中时,它会增强单加氧酶的活性,如芳烃羟化酶、乙氧香豆素O - 脱烷基酶和苄非他明N - 脱甲基酶。在用苯巴比妥或3 - 甲基胆蒽处理过的或未处理的大鼠制备的微粒体中均能观察到这种增强作用。据信添加的还原酶会掺入微粒体膜中,其掺入速率可通过测量乙氧香豆素脱烷基酶活性的增强来测定。在37℃下孵育30分钟才能实现最大掺入,在较低温度下该过程要慢得多。温度影响掺入速率,但不影响掺入程度。掺入后,可通过用琼脂糖4B柱进行凝胶过滤将富集的微粒体与未结合的还原酶分离。已研究了添加的还原酶、结合的还原酶与羟化酶活性增强之间的关系。还用胰蛋白酶处理过的微粒体研究了还原酶水平与芳烃羟化酶活性之间的关系。胰蛋白酶处理会从微粒体中去除还原酶,还原酶活性的降低伴随着芳烃羟化酶活性的平行降低。当添加纯化的还原酶时,经处理的微粒体能够获得与正常微粒体相当的芳烃羟化酶活性水平。本研究表明,纯化的NADPH - 细胞色素P - 450还原酶可掺入微粒体膜中,掺入的还原酶可与膜中的细胞色素P - 450分子相互作用,可能与内源性还原酶分子的作用方式相同。该结果与微粒体膜中细胞色素P - 450和NADPH - 细胞色素P - 450还原酶组织的非刚性模型一致。