O'Neil Lauren L, Wiest Olaf
Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, 46556-5670, USA.
Org Biomol Chem. 2008 Feb 7;6(3):485-92. doi: 10.1039/b713318a. Epub 2007 Dec 13.
Base flipping is the movement of a DNA base from an intrahelical, base-stacked position to an extrahelical, solvent-exposed position. As there are favorable interactions for an intrahelical base, both hydrogen bonding and base stacking, base flipping is expected to be energetically prohibitive for an undamaged DNA duplex. For damaged DNA bases, however, the energetic cost of base flipping may be considerably lower. Using a selective, non-covalent assay for base flipping, the sequence dependence of base flipping in DNA sequences containing an abasic site has been studied. The dissociation constants of the zinc-cyclen complex to small molecules and single strands of DNA as well as the equilibrium constants for base flipping have been determined for these sequences. Molecular dynamics simulations of the zinc-cyclen complex bound to both single- and double-stranded DNA have been performed in an attempt to rationalize the differences in the dissociation constants obtained for the two systems. The results are compared to previous studies of base flipping in DNA containing an abasic site.
碱基翻转是指DNA碱基从螺旋内的碱基堆积位置移动到螺旋外的溶剂暴露位置。由于螺旋内碱基存在有利的相互作用,包括氢键和碱基堆积,因此对于未受损的DNA双链体,碱基翻转在能量上应该是被禁止的。然而,对于受损的DNA碱基,碱基翻转的能量成本可能会低得多。通过使用一种用于碱基翻转的选择性非共价测定法,研究了含有无碱基位点的DNA序列中碱基翻转的序列依赖性。已经确定了锌-环烯配合物与小分子和单链DNA的解离常数以及碱基翻转的平衡常数。对与单链和双链DNA结合的锌-环烯配合物进行了分子动力学模拟,试图解释两个系统获得的解离常数差异。将结果与先前对含有无碱基位点的DNA中碱基翻转的研究进行了比较。