Pearlman D A, Kollman P A
Department of Pharmaceutical Chemistry, University of California, San Francisco 94143-0446.
Biopolymers. 1990;29(8-9):1193-209. doi: 10.1002/bip.360290810.
We have examined the free energy effects of 5-methylation of cytosine on the B in equilibrium Z conformational equilibrium in DNA. Free energy differences were calculated using the free energy perturbation approach, which uses an easily derived equation from classical statistical mechanics to relate the free energy difference between two states to the ensemble average of the potential energy difference between the states. Calculations were carried both in explicit solvent and (for comparison) in vacuo. The free energy values obtained for the explicit solvent systems are total free energies, with contributions from all parts of the system (solvent + solute), and so are relevant to the B in equilibrium Z transitions observed under real (physiological) conditions. We calculate that in solution, methylation makes the B in equilibrium Z transition more favorable by about -0.4 kcal/mole base pair (bp) in free energy. This value compares well with approximate experimentally derived values of about -0.3 kcal/mole-bp. We also discuss a method for determining the free energy difference between conformational states poorly maintained by a potential energy model. Finally, the effects of methylation on the melting temperature of DNA are examined.
我们研究了胞嘧啶5 - 甲基化对DNA中B型与Z型平衡构象转变的自由能效应。自由能差异采用自由能微扰方法计算,该方法利用经典统计力学中一个易于推导的方程,将两个状态之间的自由能差异与状态之间势能差异的系综平均值联系起来。计算分别在显式溶剂中以及(为作比较)在真空中进行。显式溶剂系统获得的自由能值是总自由能,包含系统所有部分(溶剂 + 溶质)的贡献,因此与在实际(生理)条件下观察到的B型与Z型转变相关。我们计算得出,在溶液中,甲基化使B型与Z型平衡转变在自由能上更有利,每碱基对(bp)约为 -0.4千卡/摩尔。该值与约 -0.3千卡/摩尔 - bp的近似实验推导值相当吻合。我们还讨论了一种确定由势能模型维持不佳的构象状态之间自由能差异的方法。最后,研究了甲基化对DNA解链温度的影响。