Sivolob A V, Khrapunov S N
Mol Biol (Mosk). 1988 Mar-Apr;22(2):414-22.
The electrostatic interaction of extended cationic ligands with DNA has been considered on the basis of the analytical solution of a simplified Poisson--Boltzmann equation for the charged polyion cylinder. The control numerical solution of rigorous Poisson--Boltzmann equation shows that the assumption about the absence of coions in the vicinity of the highly charged polyion cylinder does not significantly influence the accuracy of solution and DNA electrostatic free energy evaluation. It was found that the basic contribution to the free energy of electrostatic ligand-DNA interaction is the mixing entropy change due to release of counterions from the vicinity of DNA. The equation for the dependence of the ligand to DNA binding constant K upon ionic strength c has been derived without introduction of any empirical parameters. This equation is consistent with the experimental data and can be used for the determination of a number of ligand--DNA ionic contacts in a wide range of salt concentrations. The main consequences of Manning and Record et al. theories can be considered as limiting cases of the theory presented. In particular the equation d(lnK)/d(lnc) = -0.88 N by Record et al. has a restricted range of application and it can be used only for a relative approximate estimation of the number of electrostatic bonds in ligand-DNA complexes. The analysis of electrostatic interaction of DNA with ligands which neutralize only part of phosphate groups in the binding site of DNA was also performed.(ABSTRACT TRUNCATED AT 250 WORDS)
基于带电多离子圆柱体简化泊松 - 玻尔兹曼方程的解析解,研究了扩展阳离子配体与DNA的静电相互作用。严格泊松 - 玻尔兹曼方程的控制数值解表明,关于高电荷多离子圆柱体附近不存在共离子的假设,对解的准确性和DNA静电自由能评估的影响并不显著。研究发现,静电配体 - DNA相互作用自由能的主要贡献是由于反离子从DNA附近释放导致的混合熵变。在不引入任何经验参数的情况下,推导了配体与DNA结合常数K随离子强度c变化的方程。该方程与实验数据一致,可用于在广泛的盐浓度范围内确定一些配体 - DNA离子接触。曼宁和雷科德等人理论的主要结果可被视为所提出理论的极限情况。特别是雷科德等人的方程d(lnK)/d(lnc) = -0.88 N的应用范围有限,仅可用于相对近似地估计配体 - DNA复合物中静电键的数量。还对DNA与仅中和DNA结合位点部分磷酸基团的配体的静电相互作用进行了分析。(摘要截于250字)