Ro J Y, Jensen D E, Kim S
Cancer Lett. 1984 Jun;23(2):213-21. doi: 10.1016/0304-3835(84)90156-3.
The O6-methylguanine-DNA:methyltransferase is known to transfer the methyl group from O6-methylguanine (O6-mG) in DNA to the cysteinyl residue of the methyl acceptor protein which is the methyltransferase itself. We developed a novel method to estimate the amount of S-methylcysteine formed in the acceptor protein, utilizing O6-[methyl-3H]methylguanine-containing DNA as the methyl donor. Following hydrolysis of the methyl-incorporated macromolecules in formic acid--HCl, S-[methyl-3H]methylcysteine is chromatographically isolated on a small column of Dowex-50(H+). Utilizing this method, we measured O6-mG DNA:methyltransferase activity in rat liver during neonatal development; the activity increases from 0.013 pmol methyl transferred/mg protein at 2 days postnatally to 0.06 pmol/mg at 8 weeks, the latter being equal to the adult liver activity.
已知O6-甲基鸟嘌呤-DNA甲基转移酶可将DNA中O6-甲基鸟嘌呤(O6-mG)的甲基转移至甲基受体蛋白的半胱氨酰残基上,而甲基受体蛋白本身就是甲基转移酶。我们开发了一种新方法来估算受体蛋白中形成的S-甲基半胱氨酸的量,该方法利用含O6-[甲基-3H]甲基鸟嘌呤的DNA作为甲基供体。在用甲酸-HCl水解掺入甲基的大分子后,S-[甲基-3H]甲基半胱氨酸通过在一小柱Dowex-50(H+)上进行色谱分离。利用该方法,我们测定了新生大鼠肝脏在发育过程中的O6-mG DNA甲基转移酶活性;该活性从出生后2天的0.013皮摩尔甲基转移/毫克蛋白增加到8周时的0.06皮摩尔/毫克,后者与成年肝脏活性相当。