Bostock-Smith C E, Harris S A, Laughton C A, Searle M A
Department of Chemistry and School of Pharmaceutical Sciences, University Park, Nottingham NG7 2RD, UK.
Nucleic Acids Res. 2001 Feb 1;29(3):693-702. doi: 10.1093/nar/29.3.693.
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.
对d(GGTAATTACC)(2)及其与Hoechst 33258的四氢嘧啶类似物形成的复合物进行核磁共振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契合的结合,而不是与预先组织好的位点结合。对结合态和未结合态结构波动的分析表明,观察到的诱导契合程度主要是优化与小沟壁范德华接触的结果,导致小沟变窄,具体方式如下:(i) 碱基步参数的变化,包括螺旋扭转和螺旋桨扭转增加;(ii) 糖-磷酸主链构象的变化以包围结合的配体;(iii) TpA步处弯曲模式的抑制。相比之下,小沟底部氢键受体的几何排列似乎对DNA构象(螺旋扭转和螺旋桨扭转)相对不敏感。我们认为,对DNA序列(在这种情况下是A序列结构)的有效识别在很大程度上似乎取决于该序列具有足够的灵活性,能够采用与各种结合相互作用兼容的几何最优构象,而不是涉及“锁钥”识别。