Sagstuen E, Hole E O, Nelson W H, Close D M
Department of Physics, University of Oslo, Norway.
Radiat Res. 1988 Nov;116(2):196-209.
Single crystals of the free base of guanosine 5'-monophosphate were X-irradiated at 10 and at 65 K and investigated between these temperatures and room temperature using K-band ESR and ENDOR spectroscopy. Three free radicals were detected in this temperature range. Two of these were identified as the O6-protonated anion radical and the C8 H-addition radical. Both of these species were present immediately after irradiation at 10 K. The anion radical was formed in two slightly different conformations, of which one decayed at about 150 K and the second at about 250 K. No successor radicals could be detected following the decay of the anion radical. The C8 H-adduct was stable at all temperatures used. The use of partially deuterated crystals confirmed the assignments made and showed that the main pathway for the formation of the C8 H-adduct consisted of addition of a proton from an easily exchangeable site. It is suggested that the C8 H-adduct is formed subsequent to a primary oxidation event localized either at the guanine base or at a nearby water of crystallization. Possible mechanisms for the formation of this product are discussed.
5'-磷酸鸟苷游离碱的单晶在10K和65K下进行X射线辐照,并在这些温度与室温之间使用K波段电子顺磁共振(ESR)和电子核双共振(ENDOR)光谱进行研究。在此温度范围内检测到了三种自由基。其中两种被鉴定为O6-质子化阴离子自由基和C8 H-加成自由基。这两种物种在10K辐照后立即存在。阴离子自由基以两种略有不同的构象形成,其中一种在约150K时衰减,另一种在约250K时衰减。阴离子自由基衰减后未检测到后续自由基。C8 H-加合物在所有使用的温度下均稳定。使用部分氘代晶体证实了所做的归属,并表明C8 H-加合物形成的主要途径包括从易于交换的位点添加一个质子。有人认为,C8 H-加合物是在鸟嘌呤碱基或附近结晶水处发生的一次初级氧化事件之后形成的。讨论了该产物形成的可能机制。