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有氧和无氧条件下单链嘧啶多核苷酸中辐射诱导链断裂形成的动力学;时间分辨光散射研究

Kinetics of radiation-induced strand break formation in single-stranded pyrimidine polynucleotides in the presence and absence of oxygen; a time-resolved light-scattering study.

作者信息

Jones G D, O'Neill P

机构信息

Division of Molecular Processes, Medical Research Council Radiobiology Unit, Didcot, Oxon, UK.

出版信息

Int J Radiat Biol. 1991 May;59(5):1127-45. doi: 10.1080/09553009114551031.

Abstract

Time-resolved reductions in the light-scattering intensity (LSI) of aqueous oxic and anoxic solutions of poly-C and poly-U at pH 7.8, following pulse-irradiation, have been studied as indices of strand break formation. With doses of 3-24 Gy per pulse, a number of kinetically distinct strand breakage components have been detected. A comparison of the LSI responses obtained from irradiations conducted under N2O with those conducted under air or O2 show no marked difference in the overall extent of LSI change. However, the immediate and fast (t 1/2 less than or equal to 50 microseconds) reduction in LSI, accounting for about 18-19% of the pyrimidine polynucleotide's total LSI response in oxic solution, is reduced in the absence of oxygen, to about 12% of the total LSI response found with poly-C and to about 9% for poly-U. For poly-C there is a five-fold enhancement in the rate of major strand breakage under anoxia [k1(N2O) = 7.9s-1] whereas for poly-U a more modest enhancement (about two-fold) is observed. These enhanced rates are mirrored by those for the losses of the principal optical anoxic absorptions (observed pulse radiolytically) that are assigned to the pyrimidine 6-yl base radicals. Such findings support a proposal that the rate-limiting step of major strand breakage for pyrimidine polynucleotides is a base radical mediated hydrogen atom abstraction reaction (Lemaire et al. 1987, Hildenbrand and Schulte-Frohlinde 1989). Irradiation of poly-C and poly-U in N2O/O2 (4:1, v/v) saturated solutions yields LSI changes much larger than those noted under N2O and air (or O2), which are in turn approximately double the responses observed under N2. This indicates that the major strand breaking species of water radiolysis is the OH-radical and that there is an oxygen enhancement of single strand breakage of about 1.9 for poly-C and 1.6 for poly-U.

摘要

在pH 7.8条件下,对聚胞嘧啶(poly-C)和聚尿嘧啶(poly-U)的有氧和无氧水溶液进行脉冲辐照后,研究了其光散射强度(LSI)随时间的变化,以此作为链断裂形成的指标。每脉冲剂量为3 - 24 Gy时,检测到了一些动力学上不同的链断裂成分。比较在一氧化二氮(N₂O)、空气或氧气条件下辐照得到的LSI响应,发现LSI变化的总体程度没有明显差异。然而,在有氧溶液中,LSI的即时快速降低(t₁/₂≤50微秒)约占嘧啶多核苷酸总LSI响应的18 - 19%,在无氧条件下,这一比例降至约占聚胞嘧啶总LSI响应的12%,聚尿嘧啶为约9%。对于聚胞嘧啶,缺氧条件下主要链断裂速率提高了五倍[k₁(N₂O)=7.9 s⁻¹],而对于聚尿嘧啶,观察到的提高幅度较小(约两倍)。这些提高的速率与主要光学无氧吸收损失的速率相对应(通过脉冲辐解观察到),这些吸收归因于嘧啶6 - 基自由基。这些发现支持了一个提议,即嘧啶多核苷酸主要链断裂的限速步骤是碱基自由基介导的氢原子夺取反应(勒梅尔等人,1987年;希尔登布兰德和舒尔特 - 弗罗林德,1989年)。在N₂O/氧气(4:1,v/v)饱和溶液中辐照聚胞嘧啶和聚尿嘧啶产生的LSI变化比在N₂O和空气(或氧气)条件下观察到的大得多,而后者又大约是在氮气条件下观察到的响应的两倍。这表明水辐射分解的主要链断裂物种是羟基自由基(OH·),并且聚胞嘧啶的单链断裂存在约1.9倍的氧增强效应,聚尿嘧啶为1.6倍。

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