Tadokoro K, Ishidate K, Nakazawa Y
Biochim Biophys Acta. 1985 Jul 31;835(3):501-13.
New evidence is provided that rat liver choline kinase exists in several distinct forms (choline kinases I, II and III) which differ in isoelectric point, molecular size and antigenicity against anti-rat kidney choline kinase IgG. Remarkable and selective induction of the choline kinase II and choline kinase III forms of choline kinase was caused similarly by the administration of polycyclic aromatic hydrocarbon carcinogen, 3-methylcholanthrene or hepatotoxic carbon tetrachloride (CCl4). The immunochemical approach further indicated that the elevation in the activity of choline kinase in the 3-methylcholanthrene- or CCl4-treated rat liver was not accompanied by a parallel increase in the amount of choline kinase II enzyme protein, compatible with the induction of either a small amount of new enzyme protein(s) with very high specific activity or another enzyme which might catalyze post-translational modification of choline kinase.
有新证据表明,大鼠肝脏胆碱激酶存在几种不同形式(胆碱激酶I、II和III),它们在等电点、分子大小以及针对抗大鼠肾脏胆碱激酶IgG的抗原性方面存在差异。多环芳烃致癌物3 - 甲基胆蒽或肝毒性四氯化碳(CCl4)的给药同样会引起胆碱激酶的胆碱激酶II和胆碱激酶III形式显著且选择性的诱导。免疫化学方法进一步表明,在经3 - 甲基胆蒽或CCl4处理的大鼠肝脏中,胆碱激酶活性的升高并未伴随胆碱激酶II酶蛋白量的平行增加,这与诱导出少量具有非常高比活性的新酶蛋白或另一种可能催化胆碱激酶翻译后修饰的酶相一致。