Caldwell J W, Kollman P A
Department of Pharmaceutical Chemistry, School of Pharmacy, University of California, San Francisco 94143.
J Biomol Struct Dyn. 1985 Aug;3(1):57-66. doi: 10.1080/07391102.1985.10508398.
The effect of methylation of the O-6 position of guanine in short segments of double helical DNA has been investigated by molecular mechanical simulations on the sequences d(CGCGCG)2, d(CGC[OMG]CG)2, d(CGT[OMG]CG)2, d(CGC[OMC]CG/(CGCGCG), d(CGC[OMG]CG/d(CGTGCG), d(CGCGAATTCGCG)2 and d(CGCGAATTC[OMG]CG)2. Guanines methylated at the O-6 position are found to form hydrogen bonds of roughly equal strength to cytosine and thymine. The optimum structure of these modified base pairs are not dramatically different from normal GC pairs, but both involve some bifurcation of the proton donors of cytosine (4NH2) or thymine (3NH) between the guanine N3 and O6 groups.
通过对序列d(CGCGCG)2、d(CGC[OMG]CG)2、d(CGT[OMG]CG)2、d(CGC[OMC]CG/(CGCGCG)、d(CGC[OMG]CG/d(CGTGCG)、d(CGCGAATTCGCG)2和d(CGCGAATTC[OMG]CG)2进行分子力学模拟,研究了双链DNA短片段中鸟嘌呤O-6位甲基化的影响。发现O-6位甲基化的鸟嘌呤与胞嘧啶和胸腺嘧啶形成强度大致相等的氢键。这些修饰碱基对的最佳结构与正常GC对没有显著差异,但两者都涉及胞嘧啶(4NH2)或胸腺嘧啶(3NH)的质子供体在鸟嘌呤N3和O6基团之间的某种分叉。