首页> 美国卫生研究院文献>Nucleic Acids Research >Induced fit DNA recognition by a minor groove binding analogue of Hoechst 33258: fluctuations in DNA A tract structure investigated by NMR and molecular dynamics simulations
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Induced fit DNA recognition by a minor groove binding analogue of Hoechst 33258: fluctuations in DNA A tract structure investigated by NMR and molecular dynamics simulations

机译:Hoechst 33258的小沟结合类似物诱导的fit DNA识别: 通过NMR和分子动力学模拟研究的DNA A道结构

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摘要

NMR analysis and molecular dynamics simulations of d(GGTAATTACC)2 and its complex with a tetrahydropyrimidinium analogue of Hoechst 33258 suggest that DNA minor groove recognition in solution involves a combination of conformational selection and induced fit, rather than binding to a preorganised site. Analysis of structural fluctuations in the bound and unbound states suggests that the degree of induced fit observed is primarily a consequence of optimising van der Waals contacts with the walls of the minor groove resulting in groove narrowing through: (i) changes in base step parameters, including increased helical twist and propeller twist; (ii) changes to the sugar–phosphate backbone conformation to engulf the bound ligand; (iii) suppression of bending modes at the TpA steps. In contrast, the geometrical arrangement of hydrogen bond acceptors on the groove floor appears to be relatively insensitive to DNA conformation (helical twist and propeller twist). We suggest that effective recognition of DNA sequences (in this case an A tract structure) appears to depend to a significant extent on the sequence being flexible enough to be able to adopt the geometrically optimal conformation compatible with the various binding interactions, rather than involving ‘lock and key’ recognition.
机译:d(GGTAATTACC)2及其与Hoechst 33258的四氢嘧啶类似物的配合物的NMR分析和分子动力学模拟表明,溶液中的DNA小沟识别涉及构象选择和诱导拟合的结合,而不是结合到预定位点。对束缚态和未束缚态的结构性波动的分析表明,观察到的感应配合程度主要是优化Van der Waals与次要凹槽壁的接触的结果,从而通过以下方式导致凹槽变窄:(i)基本阶跃参数的变化,包括增加的螺旋扭曲和螺旋桨扭曲; (ii)改变糖-磷酸骨架的构象以吞噬结合的配体; (iii)在TpA步骤抑制弯曲模式。相反,凹槽底部的氢键受体的几何排列似乎对DNA构象(螺旋扭曲和螺旋桨扭曲)相对不敏感。我们建议,DNA序列(在这种情况下为A链结构)的有效识别似乎在很大程度上取决于该序列是否足够灵活以能够采用几何 与各种结合相互作用兼容的最佳构象, 而不是涉及“锁定和钥匙”识别。

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