Waldstein E A, Cao E H, Setlow R B
Nucleic Acids Res. 1982 Aug 11;10(15):4595-604. doi: 10.1093/nar/10.15.4595.
We have assayed in extracts of HeLa cells the amount of acceptor protein that removes O6-methylguanine adducts from alkylated DNA. Cells were treated with single or multiple nontoxic doses of N-methyl-N'-nitrosoguanidine (MNNG) and the extracts were analyzed up to 32 h after the last exposure. The acceptor activity assayed immediately (1 h) after single exposures decreases linearly with dose indicating that the acceptor protein is used up by endogenous O6-methylguanine adducts in a stoichiometric reaction. Multiple exposures, assayed 8-24 h after the last exposure, increase the amount of acceptor protein in a dose dependent fashion followed by a decrease above a cumulative dose of 100 ng/ml. Under conditions of maximum induction, there are about 300,000 acceptor protein sites per cell, approximately 3 fold above the constitutive level. Both in adapted and unadapted cells the methyl group from O6-methylguanine adducts in the alkylated DNA is transferred to cysteine residues of the acceptor protein(s).
我们已经在HeLa细胞提取物中检测了从烷基化DNA上去除O6-甲基鸟嘌呤加合物的受体蛋白量。细胞用单次或多次无毒剂量的N-甲基-N'-亚硝基胍(MNNG)处理,并且在最后一次暴露后长达32小时对提取物进行分析。单次暴露后立即(1小时)检测的受体活性随剂量呈线性下降,这表明受体蛋白在化学计量反应中被内源性O6-甲基鸟嘌呤加合物耗尽。多次暴露后,在最后一次暴露后8-24小时进行检测,受体蛋白量以剂量依赖方式增加,随后在累积剂量超过100 ng/ml时下降。在最大诱导条件下,每个细胞约有300,000个受体蛋白位点,比组成水平高约3倍。在适应和未适应的细胞中,烷基化DNA中O6-甲基鸟嘌呤加合物的甲基都转移到受体蛋白的半胱氨酸残基上。