Kuwabara M, Hiraoka W, Sato F
Department of Radiation Biology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Biochemistry. 1989 Dec 12;28(25):9625-32. doi: 10.1021/bi00451a013.
A method combining spin trapping, ESR, and HPLC was employed to obtain evidence for the formation of sugar radicals in OH-attacked TMP with special emphasis on the detection of strand-break precursors of DNA. OH radicals were produced by irradiating an N2O-saturated aqueous solution with X-rays. When an N2O-saturated aqueous solution containing TMP and a spin trapping reagent, MNP, was irradiated with X-rays, it was estimated on the basis of theoretical calculations using rate constants that 94% of the TMP radicals were induced by OH radicals. Since several spin adducts between TMP radicals and MNP, as well as the byproducts of the spin trapping reagent itself, were produced, reverse-phase HPLC was used to separate them. The presence of six spin adducts was confirmed by ESR examination. Further examination of these spin adducts by UV absorbance spectrophotometry showed the presence of a chromophore at 260 nm in three adducts. Since a gradual increase in the release of unaltered base from these adducts was observed when they were allowed to stand for 0-22 h at room temperature, they could be regarded as the spin adducts of sugar radicals and MNP. ESR spectra from the spin adducts were consistent with hydrogen abstraction radicals at the C1', C4', and C5' positions of the sugar moiety. These radicals appeared to be precursors of AP sites and strand breaks. In addition to these spin adducts, ESR spectra that were consistent with the spin adducts of base radicals (the C5 and C6 radicals) and MNP were observed.
采用自旋捕获、电子自旋共振(ESR)和高效液相色谱(HPLC)相结合的方法来获取证据,以证明在羟基攻击的胸腺嘧啶核苷酸(TMP)中糖自由基的形成,特别着重于检测DNA链断裂前体。通过用X射线照射N₂O饱和水溶液来产生羟基自由基。当用X射线照射含有TMP和自旋捕获试剂MNP的N₂O饱和水溶液时,根据使用速率常数的理论计算估计,94%的TMP自由基是由羟基自由基诱导产生的。由于产生了TMP自由基与MNP之间的几种自旋加合物以及自旋捕获试剂本身的副产物,因此使用反相HPLC对它们进行分离。通过ESR检测确认了六种自旋加合物的存在。通过紫外吸收分光光度法对这些自旋加合物的进一步检测表明,三种加合物在260 nm处存在发色团。由于当这些加合物在室温下放置0 - 22小时时,观察到未改变碱基的释放逐渐增加,因此它们可被视为糖自由基与MNP的自旋加合物。自旋加合物的ESR光谱与糖部分C1'、C4'和C5'位置的氢提取自由基一致。这些自由基似乎是脱嘌呤嘧啶位点(AP位点)和链断裂的前体。除了这些自旋加合物外,还观察到与碱基自由基(C5和C6自由基)和MNP的自旋加合物一致的ESR光谱。