首页> 美国卫生研究院文献>Nucleic Acids Research >Structure of a bis-amidinium derivative of Hoechst 33258 complexed to dodecanucleotide d(CGCGAATTCGCG) 2 : the role of hydrogen bonding in minor groove drug-DNA recognition
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Structure of a bis-amidinium derivative of Hoechst 33258 complexed to dodecanucleotide d(CGCGAATTCGCG) 2 : the role of hydrogen bonding in minor groove drug-DNA recognition

机译:Hoechst 33258的双ami衍生物与十二核苷酸d(CGCGAATTCGCG)2复合的结构:氢键在小沟药物-DNA识别中的作用

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摘要

The crystal structure is reported of a complex between the dodecanucleotide sequence d(CGCGAATTCGCG)2and an analogue of the DNA binding drug Hoechst 33258, in which the piperazine ring has been replaced by an amidinium group and the phenol ring by a phenylamidinium group. The structure has been refined to an R factor of 19.5% at 2.2 A resolution. The drug is held in the minor groove by five strong hydrogen bonds, together with bridging water molecules at both ends. There are few other contacts with the floor of the groove, indicating a lack of isohelicity with the groove and suggesting (i) that the observed high DNA affinity of this drug is primarily due to the array of hydrogen bonds and (ii) that these more than compensate for its poor isohelicity.
机译:据报道该晶体结构是十二核苷酸序列d(CGCGAATTCGCG)2与DNA结合药物Hoechst 33258的类似物之间的复合物,其中哌嗪环被by基取代,苯酚环被苯ami基取代。该结构在2.2 A分辨率下已精炼到19.5%的R系数。该药物通过五个强氢键以及两端的桥连水分子保持在小沟中。与凹槽底部几乎没有其他接触,表明与凹槽之间没有等渗性,这表明(i)观察到的该药物的高DNA亲和力主要是由于氢键的排列所致;(ii)这些更多而不是弥补其等渗性差。

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