Miller John H, Fan-Chiang Cheng-Chih P, Straatsma T P, Kennedy Michael A
Washington State University Tri-Cities, Richland 99352, USA.
J Am Chem Soc. 2003 May 21;125(20):6331-6. doi: 10.1021/ja029312n.
Molecular dynamics (MD) simulations were carried out on the DNA oligonucleotide GGGAACAACTAG:CTAGTTGTTCCC in its native form and with guanine in the central G(19):C(6) base pair replaced by 8-oxoguanine (8oxoG). A box of explicit water molecules was used for solvation, and Na(+) counterions were added to neutralize the system. The direction and magnitude of global bending were assessed by a technique used previously to analyze simulations of DNA containing a thymine dimer. The presence of 8oxoG did not greatly affect the magnitude of DNA bending; however, bending into the major groove was significantly more probable when 8oxoG replaced G(19). Crystal structures of glycosylases bound to damaged-DNA substrates consistently show a sharp bend into the major groove at the damage site. We conclude that changes in bending dynamics that assist the formation of this kink are a part of the mechanism by which glycosylases of the base excision repair pathway recognize the presence of 8oxoG in DNA.
对天然形式的DNA寡核苷酸GGGAACAACTAG:CTAGTTGTTCCC以及中心G(19):C(6)碱基对中的鸟嘌呤被8-氧代鸟嘌呤(8oxoG)取代后的该寡核苷酸进行了分子动力学(MD)模拟。使用一箱明确的水分子进行溶剂化,并添加Na(+)抗衡离子以中和系统。通过先前用于分析含胸腺嘧啶二聚体DNA模拟的技术评估全局弯曲的方向和幅度。8oxoG的存在对DNA弯曲的幅度影响不大;然而,当8oxoG取代G(19)时,向大沟弯曲的可能性显著增加。与受损DNA底物结合的糖基化酶的晶体结构始终显示在损伤位点向大沟急剧弯曲。我们得出结论,有助于形成这种扭结的弯曲动力学变化是碱基切除修复途径的糖基化酶识别DNA中8oxoG存在的机制的一部分。