Kohn K W, Ewig R A
Biochim Biophys Acta. 1979 Mar 28;562(1):32-40. doi: 10.1016/0005-2787(79)90123-0.
DNA-protien crosslinks produced in mouse leukemia L1210 cells by trans-Pt(II)diamminedichloride were quantitated using the technique of DNA alkaline elution. DNA single-strand segments that were or were not linked to protein were separable into distinct components by alkaline elution after exposure of the cells to 2--15 kR of X-ray. Protein-linked DNA strands were separated on the basis of their retention of filters at pH 12 while free DNA strands of the size generated by 2--15 kR of X-ray passed rapidly through the filters. The retention of protein-linked DNA strands was attributable to adsorption of protein to the filter under the conditions of alkaline elution. The results obeyed a simple quantitative model according to which the frequency of DNA-protein crosslinks could be calculated.
使用DNA碱性洗脱技术对反式二氯二氨合铂(II)在小鼠白血病L1210细胞中产生的DNA-蛋白质交联进行定量。在细胞接受2-15 kR的X射线照射后,通过碱性洗脱可将与蛋白质相连或未相连的DNA单链片段分离成不同的组分。蛋白质连接的DNA链基于其在pH 12时在滤膜上的保留情况进行分离,而由2-15 kR的X射线产生的大小的游离DNA链则迅速通过滤膜。蛋白质连接的DNA链的保留归因于碱性洗脱条件下蛋白质在滤膜上的吸附。结果符合一个简单的定量模型,据此可计算DNA-蛋白质交联的频率。