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修饰核苷酸形成的DNA链间交联:机制与应用

DNA interstrand cross-links from modified nucleotides: mechanism and application.

作者信息

Greenberg Marc M

机构信息

Johns Hopkins University, Department of Chemistry, 3400 N. Charles St., Baltimore, MD 21218, USA.

出版信息

Nucleic Acids Symp Ser (Oxf). 2005(49):57-8. doi: 10.1093/nass/49.1.57.

Abstract

Interstrand DNA cross-links are believed to be the source of cytotoxicity of antitumor agents such as mitomycin C and nitrogen mustards. We observed the first example in which DNA-DNA cross-links result from the reaction of a DNA radical. 5-(2'-Deoxyuridinyl)methyl radical (1) is produced during gamma-irradiation of DNA and other methods of oxidative stress. Independent generation of this reactive intermediate in duplex DNA results in significant levels of interstrand cross-links. Cross-link formation does not require O2 and involves reaction between the nucleotide where the radical is originally generated and the opposing deoxyadenosine. Mechanistic studies have led to the identification of other molecules that produce interstrand DNA cross-links via 1. In addition, other methods for producing interstrand DNA cross-links via the radical precursor have been discovered that may be therapeutically useful.

摘要

链间DNA交联被认为是丝裂霉素C和氮芥等抗肿瘤药物细胞毒性的来源。我们观察到了首个DNA自由基反应产生DNA-DNA交联的例子。5-(2'-脱氧尿苷基)甲基自由基(1)在DNA的γ射线照射及其他氧化应激方法过程中产生。在双链DNA中独立生成这种反应性中间体可导致显著水平的链间交联。交联的形成不需要氧气,且涉及自由基最初产生位置的核苷酸与对面的脱氧腺苷之间的反应。机理研究已鉴定出其他通过1产生链间DNA交联的分子。此外,还发现了其他通过自由基前体产生链间DNA交联的方法,这些方法可能具有治疗用途。

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