...
首页> 外文期刊>Future medicinal chemistry >C8-linked bulky guanosine DNA adducts: Experimental and computational insights into adduct conformational preferences and resulting mutagenicity
【24h】

C8-linked bulky guanosine DNA adducts: Experimental and computational insights into adduct conformational preferences and resulting mutagenicity

机译:C8连接的庞大的鸟苷DNA加合物:对加合物构象偏好和诱变性的实验和计算见解

获取原文
获取原文并翻译 | 示例

摘要

Bulky DNA adducts are formed through the covalent attachment of aryl groups to the DNA nucleobases. Many of these adducts are known to possess conformational heterogeneity, which is responsible for the variety of mutagenic outcomes associated with these lesions. The present contribution reviews several conformational and mutagenic themes that are prevalent among the DNA adducts formed at the C8-site of the guanine nucleobase. The most important conclusions obtained (to date) from experiments are summarized including the anti/syn conformational preference of the adducts, their potential to inflict DNA mutations and mismatch stabilization, and their interactions with DNA polymerases and repair enzymes. Additionally, the unique role that computer calculations can play in understanding the structural properties of these adducts are highlighted.
机译:庞大的DNA加合物是通过芳基与DNA核碱基的共价连接形成的。已知许多这些加合物具有构象异质性,这是导致与这些病变相关的多种诱变结果的原因。本贡献回顾了在鸟嘌呤核苷碱基的C8位点形成的DNA加合物中普遍存在的几个构象和诱变主题。从实验中获得(迄今为止)最重要的结论,包括加合物的抗/顺式构象偏爱,它们造成DNA突变和错配稳定的潜力以及它们与DNA聚合酶和修复酶的相互作用。此外,强调了计算机计算在理解这些加合物的结构性质中可以发挥的独特作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号