Sohn D H, Yun Y P, Park K S, Veech R L, Song B J
Laboratory of Metabolism and Molecular Biology, National Institute on Alcoholism, Rockville, MD 20852.
Biochem Biophys Res Commun. 1991 Aug 30;179(1):449-54. doi: 10.1016/0006-291x(91)91391-o.
The molecular mechanism of cytochrome P450IIE reduction by CCl4 was reexamined by measuring its enzyme activity, immunoreactive protein contents, and mRNA levels. Aniline hydroxylase and the amounts of immunoreactive P450IIE were rapidly decreased in a time-dependent manner after a single dose of CCl4. No changes were observed in the amounts of immunoreactive P450IIC and P450IA despite significant decreases decrease in their catalytic activities. However, the decreases in P450IIE enzyme activity and immunoreactive protein by CCl4 were not accompanied by a decline in its mRNA level. The data thus suggested a post-translational reduction of P450IIE by CCl4, probably due to specific destruction of the P450IIE protein by its own substrate rather than heme moiety.
通过测量细胞色素P450IIE的酶活性、免疫反应性蛋白含量和mRNA水平,重新研究了四氯化碳还原细胞色素P450IIE的分子机制。单次给予四氯化碳后,苯胺羟化酶和免疫反应性P450IIE的量随时间迅速下降。尽管免疫反应性P450IIC和P450IA的催化活性显著降低,但其含量未观察到变化。然而,四氯化碳导致的P450IIE酶活性和免疫反应性蛋白的降低并未伴随着其mRNA水平的下降。因此,数据表明四氯化碳对P450IIE进行了翻译后还原,这可能是由于P450IIE蛋白被其自身底物而非血红素部分特异性破坏所致。