Hawkins R B, Ginsberg D M
Biophys J. 1971 May;11(5):398-413. doi: 10.1016/S0006-3495(71)86224-0.
Coliphage T7 was exposed to (60)Co gamma radiation while suspended in phosphate buffer or in phosphate buffer plus 0.001 M l-histidine. DNA was isolated from the phage by incubation with pronase, followed by extraction with cold phenol. The intrinsic viscosity of the DNA was measured as a function of radiation dose. The fraction of DNA molecules surviving radiation treatment with no double-strand breaks was measured from the radiation-induced heterogeneity of the DNA sedimentation boundary. From comparison of these measurements it is concluded that radiation introduces lesions other than double-strand breaks which affect the hydrodynamic properties of the DNA. In both buffer and buffer plus histidine the surviving fraction of intact virus genomes far exceeds the surviving fraction of plaque-forming units at any given dose. It was found that the decrease in intrinsic viscosity with dose is independent of the presence of histidine in the radiation medium. From this it is concluded that DNA damage is primarily due to a direct effect of radiation on the phage particle. The procedure necessary to isolate DNA from irradiated virus suggests that radiation produces covalent bonding of protein to the DNA.
将噬菌体T7悬浮于磷酸盐缓冲液或含0.001 M l-组氨酸的磷酸盐缓冲液中,然后暴露于(60)Coγ辐射下。通过用链霉蛋白酶孵育,随后用冷苯酚萃取,从噬菌体中分离出DNA。测量DNA的特性粘度作为辐射剂量的函数。根据DNA沉降边界的辐射诱导异质性,测量未发生双链断裂的辐射处理后存活的DNA分子分数。通过比较这些测量结果得出结论,辐射除了引入双链断裂外,还会引入影响DNA流体动力学性质的损伤。在任何给定剂量下,无论是在缓冲液中还是在缓冲液加组氨酸中,完整病毒基因组的存活分数都远远超过噬菌斑形成单位的存活分数。发现特性粘度随剂量的降低与辐射介质中组氨酸的存在无关。由此得出结论,DNA损伤主要是由于辐射对噬菌体颗粒的直接作用。从受辐照病毒中分离DNA所需的步骤表明,辐射会使蛋白质与DNA发生共价结合。