首页> 外文期刊>Journal of the American Chemical Society >Water-Mediated Binding of Agents that Target the DNA Minor Groove
【24h】

Water-Mediated Binding of Agents that Target the DNA Minor Groove

机译:以水为媒介的结合剂靶向DNA小沟

获取原文
获取原文并翻译 | 示例
       

摘要

Small molecule complexes with DNA that incorporate linking water molecules are rare, and the DB921-DNA complex has provided a unique and well-defined system for analysis of water-mediated binding in the context of a DNA complex. DB921 has a benzimidazole-biphenyl system with terminal amidines that results in a linear conformation that does not possess the appropriate radius of curvature to match the minor groove shape and represents a new paradigm that does not fit the classical model of minor groove interactions. To better understand the role of the bound water molecule observed in the X-ray crystal structure of the DB921 complex, synthetic modifications have been made in the DB921 structure, and the interactions of the new compounds with DNA AT sites have been evaluated with an array of methods, including DNase I footprinting, biosensor-surface plasmon resonance, isothermal titration microcalorimetry, and circular dichroism. The interaction of a key compound, which has the amidine at the phenyl shifted from the para position in DB921 to the meta position, has also been examined by X-ray crystallography. The detailed structural, thermodynamic, and kinetic results provide valuable new information for incorporation of water molecules in the design of new lead scaffolds for targeting DNA in chemical biology and therapeutic applications.
机译:具有结合了水分子的DNA的小分子复合物很少见,DB921-DNA复合物提供了一个独特且定义明确的系统,用于分析DNA复合物中水介导的结合。 DB921具有带有末端am的苯并咪唑-联苯系统,该系统导致的线性构型不具有匹配小凹槽形状的合适曲率半径,并且代表了不适合小凹槽相互作用经典模型的新范式。为了更好地理解在DB921配合物的X射线晶体结构中观察到的结合水分子的作用,已对DB921结构进行了合成修饰,并使用阵列对了新化合物与DNA AT位点的相互作用进行了评估。方法,包括DNase I足迹,生物传感器表面等离振子共振,等温滴定微量热法和圆二色性。还已经通过X射线晶体学检查了键化合物的相互作用,该键化合物的苯基上的am从DB921的对位转移至间位。详细的结构,热力学和动力学结果为在化学生物学和治疗应用中靶向DNA的新型铅支架设计中引入水分子提供了有价值的新信息。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2011年第26期|p.10171-10183|共13页
  • 作者单位

    Stephen Neidle;

    Stephen Neidle;

    INSERM U-837, Jean-Pierre Aubert Research Center (JPARC), Team 4 Molecular and Cellular Targeting for Cancer Treatment,Institut de Recherches sur le Cancer de Lille, Place de Verdun, Lille 59045, France,Universite Lille-Nord de France, Lille, 59045, France;

    INSERM U-837, Jean-Pierre Aubert Research Center (JPARC), Team 4 Molecular and Cellular Targeting for Cancer Treatment,Institut de Recherches sur le Cancer de Lille, Place de Verdun, Lille 59045, France,Universite Lille-Nord de France, Lille, 59045, France;

    INSERM U-837, Jean-Pierre Aubert Research Center (JPARC), Team 4 Molecular and Cellular Targeting for Cancer Treatment,Institut de Recherches sur le Cancer de Lille, Place de Verdun, Lille 59045, France,Universite Lille-Nord de France, Lille, 59045, France;

    David W. Boykin;

    Stephen Neidle;

    Stephen Neidle;

    Stephen Neidle;

    Stephen Neidle;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:14:22

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