Gewirtz D A, Ellis A L, Randolph J K, Yanovich S, Swerdlow P S, Povirk L F, Yalowich J C
Department of Medicine, Medical College of Virginia, Richmond 23298.
Cancer Commun. 1989;1(3):175-80.
In the alkaline elution assay, expression of protein-associated DNA damage induced by topoisomerase II antagonists is facilitated by proteinase K digestion of the drug-stabilized topoisomerase-II-DNA complex. In the absence of this enzymatic deproteinization step, drug-induced DNA strand breaks are masked by the binding of the topoisomerase-II-DNA complex to the synthetic filter from which DNA is eluted subsequent to alkaline denaturation. In this manuscript, we report that as the number of cells lysed on the filter is increased, binding of the topoisomerase-II-DNA complex to the filter is compromised, permitting expression of DNA damage in the absence of enzymatic deproteinization.
在碱性洗脱试验中,拓扑异构酶II拮抗剂诱导的与蛋白质相关的DNA损伤表达,是通过蛋白酶K对药物稳定的拓扑异构酶II-DNA复合物进行消化来促进的。在没有这种酶促脱蛋白步骤的情况下,药物诱导的DNA链断裂会被拓扑异构酶II-DNA复合物与合成滤膜的结合所掩盖,DNA在碱性变性后从该滤膜上洗脱下来。在本论文中,我们报告称,随着滤膜上裂解细胞数量的增加,拓扑异构酶II-DNA复合物与滤膜的结合会受到损害,从而在没有酶促脱蛋白的情况下使DNA损伤得以表达。