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辐射诱导的DNA损伤与水合作用的关系。II. 电子损失中心导致的碱基损伤

Radiation-induced DNA damage as a function of hydration. II. Base damage from electron-loss centers.

作者信息

Swarts S G, Becker D, Sevilla M, Wheeler K T

机构信息

Department of Radiation Oncology, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27157, USA.

出版信息

Radiat Res. 1996 Mar;145(3):304-14.

PMID:8927698
Abstract

The induction of base damage products in gamma-irradiated DNA, hydrated between 2.5 and 32.8 moles of water per mole of nucleotide (tau), was investigated using the gas chromatography/mass spectrometry-selected ion monitoring technique. In general, the yields of the measured base damage products were found to be dependent on the extent of the hydration when the DNA was irradiated under nitrogen. At low hydrations (tau < or = 13), the highest yields of the measured products were found for 7,8-dihydro-8-oxo-guanine, 5,6-dihydrothymine and, to a lesser extent, 2,6-diamino-4-oxo-5-formamidopyrimidine, products which are consistent with the base radicals found in low-temperature ESR studies. At higher hydrations (tau < or = 13), changes in DNA conformation and an increase in the attack of bulk water radicals on DNA play a significant role in the formation of radiation-induced DNA base damage products. Additional findings in our study include: (1) the sum of the yields of the products formed from electron-loss centers is greater than the sum of the yields of the products formed from electron-gain centers, indicating that there might be other electron-gain products which have not been identified; (2) the combined yield for the base damage products and the release of unaltered bases at tau < or = 13 is constant, implying that radiation damage in the tightly bound water molecules of the primary hydration layer causes DNA damage (quasi-direct effect) that is similar to the damage caused by direct ionization of the DNA (direct effect); and (3) the yields of the individual base damage products that were formed from electron-loss centers can be modeled on the basis of both the known reactions that lead to the formation of the initial charged base radicals in irradiated DNA, and the known reactions that involve the conversion of these initial DNA radicals into their respective nonradical end products.

摘要

采用气相色谱/质谱选择离子监测技术,研究了在每摩尔核苷酸含2.5至32.8摩尔水(τ)的水合状态下,γ射线辐照DNA时碱基损伤产物的诱导情况。一般来说,当DNA在氮气中辐照时,所测碱基损伤产物的产率取决于水合程度。在低水合度(τ≤13)时,所测产物中7,8 - 二氢 - 8 - 氧代鸟嘌呤、5,6 - 二氢胸腺嘧啶以及程度稍低的2,6 - 二氨基 - 4 - 氧代 - 5 - 甲酰胺基嘧啶的产率最高,这些产物与低温电子顺磁共振研究中发现的碱基自由基一致。在较高水合度(τ>13)时,DNA构象的变化以及大量水自由基对DNA攻击的增加在辐射诱导的DNA碱基损伤产物形成中起重要作用。我们研究的其他发现包括:(1)由电子损失中心形成的产物产率总和大于由电子获得中心形成的产物产率总和,这表明可能存在尚未鉴定的其他电子获得产物;(2)在τ≤13时,碱基损伤产物的产率与未改变碱基的释放量之和是恒定的,这意味着初级水合层紧密结合水分子中的辐射损伤会导致与DNA直接电离(直接效应)所造成的损伤类似的DNA损伤(准直接效应);(3)由电子损失中心形成的各个碱基损伤产物的产率可以基于导致辐照DNA中初始带电碱基自由基形成的已知反应以及涉及这些初始DNA自由基转化为各自非自由基终产物的已知反应进行模拟。

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