Veselkov A N, Moroshkina E B, Soboleva O I, Frisman E V
Mol Biol (Mosk). 1984 Mar-Apr;18(2):481-7.
The comparative investigations of DNA complexes with daunomycin and proflavine were proceeded by the technique of spectrophotometry, viscometry and flow birefringence for two ionic strengths of environment (mu). According to the spectrophotometry data there is an unique type of ligand binding with DNA for mu = 0.1. The intrinsic viscosity and optical anisotropy of DNA-daunomycin complex increase nonlinearly together with its equilibrium rigidity as the amount of the binding ligand (r) rises, contrary to the behaviour of the same characteristics of DNA-proflavine complexes. The discussion of the experimental data within a scope of different models of binding reveals the best agreement with the intercalation model. Evaluation of the angels between the orientation planes of chromophore and aminoglucose residue of a daunomycin molecule and the axis of DNA double-helix was performed. Apart from intercalation there is a process of external binding of daunomycin with DNA in the low ionic strength (mu = 0.001) solutions which arises mainly at higher values of r. This type of binding weakens the long-range electrostatic interactions (and also to a certain extent the short-range ones) in DNA chain that determine the behaviour of the parameters under study.
采用分光光度法、粘度测定法和流动双折射技术,在两种离子强度(μ)的环境下,对柔红霉素和原黄素与DNA的复合物进行了对比研究。根据分光光度法数据,对于μ = 0.1,存在一种与DNA结合的独特配体类型。随着结合配体数量(r)的增加,DNA - 柔红霉素复合物的特性粘度和光学各向异性与其平衡刚性一起非线性增加,这与DNA - 原黄素复合物相同特性的行为相反。在不同结合模型范围内对实验数据的讨论表明,与嵌入模型最为吻合。对柔红霉素分子发色团和氨基葡萄糖残基的取向平面与DNA双螺旋轴之间的夹角进行了评估。除了嵌入作用外,在低离子强度(μ = 0.001)溶液中,柔红霉素与DNA还存在外部结合过程,这种结合主要在r值较高时出现。这种结合类型会削弱DNA链中决定所研究参数行为的远程静电相互作用(在一定程度上也削弱短程相互作用)。