首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Reaction of guanyl radicals in plasmid DNA with biological reductants: chemical repair of DNA damage produced by the direct effect of ionizing radiation.
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Reaction of guanyl radicals in plasmid DNA with biological reductants: chemical repair of DNA damage produced by the direct effect of ionizing radiation.

机译:质粒DNA中的鸟嘌呤自由基与生物还原剂的反应:电离辐射的直接作用产生的DNA损伤的化学修复。

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PURPOSE: It has been previously argued that the use of the one-electron oxidants (SCN)2(*-) and Br2(*-) with plasmid DNA leads to the formation of DNA guanyl radicals. These guanyl radical species are intermediates in the DNA damage produced by processes such as photo-ionization and ionizing irradiation. The present paper evaluates the use of thallium(II) ions (Tl(II)OH(+)) as the one-electron oxidant, and also determines rate constants for the reduction (repair) of guanyl radicals in plasmid DNA by a variety of reducing agents including the biologically important compounds ascorbate and glutathione. MATERIALS AND METHODS: Aqueous solutions of plasmid DNA containing 10(-3) mol dm(-3) thiocyanate or thallous ions and a reducing agent (azide, nitrite, ferrocyanide, hexachloroiridate(III), iodide, ascorbate, glutathione, glutathione disulphide, methionine, tyrosine, 5-hydroxyindole-3-acetic acid, 10(-7)-10(-4) mol dm(-3)) were irradiated with 137Cs gamma-rays (662 keV). After irradiation, the plasmid was incubated with the E. coli base excision repair endonuclease formamidopyrimidine-DNA N-glycosylase (FPG). Strand break yields after incubation were quantified by means of agarose gel electrophoresis. RESULTS: High yields of FPG-sensitive sites produced by the oxidants (SCN)2(*-) and Tl(II)OH(+) were strongly attenuated by the presence of the reducing agents. CONCLUSIONS: From the results, it is possible to arrive at estimates of the rate constants for the reduction of the DNA guanyl radical by the reducing agents. Values lie in the range 10(4)-10(7) dm(3) mol(-1) s(-1). Using the values for ascorbate and glutathione, it is possible to estimate an upper limit on the order of milliseconds for the lifetime of DNA guanyl radicals under cellular conditions. The implication is that there may well be a significant chemical repair of DNA base damage by the direct effect of ionizing radiation.
机译:用途:以前有人认为,单电子氧化剂(SCN)2(*-)和Br2(*-)与质粒DNA的使用会导致DNA鸟嘌呤基团的形成。这些鸟苷自由基物质是通过光离子化和电离辐射等过程产生的DNA损伤的中间产物。本文评估了al(II)离子(Tl(II)OH(+))作为单电子氧化剂的用途,并确定了速率常数,用于通过多种方法降低质粒DNA中鸟苷自由基的(修复)速率。还原剂,包括生物学上重要的化合物抗坏血酸和谷胱甘肽。材料与方法:含有10(-3)mol dm(-3)硫氰酸盐或亚硫酸盐离子和还原剂(叠氮化物,亚硝酸盐,亚铁氰化物,六氯铱酸盐(III),碘化物,抗坏血酸盐,谷胱甘肽,谷胱甘肽二硫化物,用137Csγ射线(662 keV)照射甲硫氨酸,酪氨酸,5-羟基吲哚-3-乙酸,10(-7)-10(-4)mol dm(-3))。辐射后,将质粒与大肠杆菌碱基切除修复内切核酸酶甲酰胺嘧啶-DNA N-糖基化酶(FPG)一起孵育。孵育后,通过琼脂糖凝胶电泳对链断裂产量进行定量。结果:氧化剂(SCN)2(*-)和Tl(II)OH(+)产生的FPG敏感位点的高产率被还原剂的存在大大削弱。结论:从结果可以得出还原剂还原DNA鸟苷自由基速率常数的估计。值在10(4)-10(7)dm(3)mol(-1)s(-1)范围内。使用抗坏血酸和谷胱甘肽的值,可以估计细胞条件下DNA胍基自由基寿命的毫秒级上限。这意味着电离辐射的直接作用很可能会对DNA碱基的损伤进行重要的化学修复。

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