Kas'ianenko N A, Valueva S V, Smorygo N A, D'iachenko S A, Frisman E V
Mol Biol (Mosk). 1995 Mar-Apr;29(2):345-53.
DNA interaction with cis-diaminodichloroplatinum (cis-DDP in solutions of different ionic strength was studied by flow birefringence, viscometry, circular dichroism. Though cis-DDP is not an electrolyte, electrostatic interactions are important for binding of cis-DDP with DNA probably for transporting cis-DDP to a macromolecule. The charges aqua-complex is formed by cis-DDP. The complexation being dependent on the platinum/DNA ratio in solution. Along with the increase of platinum concentration, it forms first the complexes with phosphate groups, then with bases without destruction of the DNA secondary structure. The next type of complex formation is accompanied by the local destruction of the hydrogen bonds and stacking interactions. And when the Pt/DNA ratio grows high enough, DNA is denatured. It is suggested that the stability of the complex is provided by nitrogen groups of the bases incorporated in the platinum first coordination sphere. The phosphate DNA groups play the role of counterions in the external coordination sphere.
通过流动双折射、粘度测定法和圆二色性研究了顺二氨基二氯铂(cis-DDP)在不同离子强度溶液中与DNA的相互作用。尽管cis-DDP不是电解质,但静电相互作用对于cis-DDP与DNA的结合可能很重要,这可能是为了将cis-DDP转运到大分子上。顺二氨基二氯铂会形成水合络合物。络合作用取决于溶液中铂/DNA的比例。随着铂浓度的增加,它首先与磷酸基团形成络合物,然后与碱基形成络合物,而不会破坏DNA的二级结构。下一种络合物形成类型伴随着氢键和堆积相互作用的局部破坏。当Pt/DNA比例足够高时,DNA会变性。有人认为,络合物的稳定性是由铂第一配位球中所含碱基的氮基团提供的。磷酸DNA基团在外部配位球中起抗衡离子的作用。