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鸟嘌呤自由基与硫氰酸盐之间的氧化还原平衡影响γ射线辐照质粒DNA中的碱基损伤产率。生理离子强度下,水溶液中质粒DNA中鸟嘌呤自由基还原电位的估算。

Redox equilibrium between guanyl radicals and thiocyanate influences base damage yields in gamma irradiated plasmid DNA. Estimation of the reduction potential of guanyl radicals in plasmid DNA in aqueous solution at physiological ionic strength.

作者信息

Milligan J R, Aguilera J A, Ward J F

机构信息

Department of Radiology, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0610, USA.

出版信息

Int J Radiat Biol. 2001 Dec;77(12):1195-205. doi: 10.1080/09553000110083988.

Abstract

PURPOSE

Gamma irradiation of an aqueous solution containing thiocyanate ions produces the strongly oxidizing intermediate (SCN)2*-. Reaction of this species with plasmid DNA produces damage that is revealed as strand breaks after incubation with the Escherichia coli base excision repair endonuclease formamidopyrimidine-DNA N-glycosylase (FPG). It has been previously reported that the yield of damage is highly sensitive to the experimental conditions, leading to the suspicion that electron transfer between DNA and (SCN)2*- is reversible. In principle this makes it possible to determine the oxidation potential for plasmid DNA (more formally the reduction potential of one-electron oxidized plasmid DNA), a fundamental parameter describing the reactivity of DNA towards electron transfer reactions.

MATERIALS AND METHODS

Aqueous solutions of plasmid DNA and thiocyanate ions were subjected to 137Cs gamma-irradiation. After irradiation, the plasmid was incubated with the E. coli base excision repair endonuclease formamidopyrimidine-DNA N-glycosylase (FPG). The yield of this damage was quantified by using agarose gel electrophoresis to identify the fraction of the plasmid population that contains strand breaks.

RESULTS

The yield of FPG-sensitive sites decreases with increasing thiocyanate concentration, decreasing DNA concentration, and increasing dose rate. By making some simple assumptions about the chemical reactions that produce DNA damage, it is possible to derive a quantitative mathematical model for the yield of FPG-sensitive sites. A good agreement was found between this model and the experimental observations over a wide range of conditions (thiocyanate concentrations, DNA concentrations, and dose rates that vary by 20-, 40-, and 150-fold respectively).

CONCLUSIONS

It was possible to assign a value to the equilibrium constant for the one electron transfer reaction between the two radical species (SCN)2*- and DNA-G*+. This leads to an estimate of the reduction potential at pH 7 for the couple DNA G*+/DNA of E7 = +1.39+/-0.01V.

摘要

目的

对含有硫氰酸根离子的水溶液进行伽马射线辐照会产生强氧化性中间体(SCN)₂⁻*。该物质与质粒DNA反应会造成损伤,在用大肠杆菌碱基切除修复内切酶甲酰胺嘧啶-DNA N-糖基化酶(FPG)孵育后,损伤表现为链断裂。此前有报道称,损伤产率对实验条件高度敏感,这引发了人们对DNA与(SCN)₂⁻*之间电子转移是否可逆的怀疑。原则上,这使得确定质粒DNA的氧化电位(更确切地说是单电子氧化质粒DNA的还原电位)成为可能,这是一个描述DNA对电子转移反应反应性的基本参数。

材料与方法

对质粒DNA和硫氰酸根离子的水溶液进行¹³⁷Cs伽马射线辐照。辐照后,将质粒与大肠杆菌碱基切除修复内切酶甲酰胺嘧啶-DNA N-糖基化酶(FPG)孵育。通过使用琼脂糖凝胶电泳来确定含有链断裂的质粒群体比例,从而对这种损伤的产率进行定量。

结果

FPG敏感位点的产率随硫氰酸根浓度增加、DNA浓度降低和剂量率增加而降低。通过对产生DNA损伤的化学反应做一些简单假设,可以推导出FPG敏感位点产率的定量数学模型。在很宽的条件范围内(硫氰酸根浓度、DNA浓度和剂量率分别变化20倍、40倍和150倍),该模型与实验观察结果吻合良好。

结论

可以为两种自由基(SCN)₂⁻*和DNA-G⁺*之间的单电子转移反应的平衡常数赋值。这得出了在pH 7时E₇ = +1.39±0.01V的DNA G⁺⁺/DNA电对还原电位的估计值。

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