Houssier C, Depauw-Gillet M C, Hacha R, Fredericq E
Biochim Biophys Acta. 1983 Apr 15;739(3):317-25. doi: 10.1016/0167-4781(83)90107-0.
The interaction of various platinum coordination complexes with nucleosomes and chromatin has been investigated by ultraviolet absorption spectrophotometry, circular and electric linear dichroism, and thermal denaturation, at low binding ratios (r less than 0.1-0.2). The general trend of the changes in these physicochemical properties is similar to that observed for the DNA-platinum complexes, which indicates that the same binding sites are involved in the platinum interaction with DNA and with its nucleoprotein complex. The cis-bidentate ligands, cis-dichlorodiammine, diaminocyclohexane and ethylenediamine platinum(II), showed a distinct behavior, with a more important destabilization of the DNA structure in the nucleoprotein than the trans-bidentate ligand, trans-dichlorodiammine-Pt(II), and monodentate ligand, diethylenetriamine-Pt(II). The drastic decrease of the negative electric dichroism in the 260 nm absorption band of the bases, observed with the five ligands, indicates a profound alteration of the DNA arrangement in chromatin and nucleosomes, attributed to a condensation of its superhelical structure. Some differences with previous observations on DNA complexes with the same platinum compounds indicate the possible formation of protein-DNA crosslinks in chromatin and nucleosomes. These could have some importance for the biological effects.
已通过紫外吸收分光光度法、圆二色性和电线性二色性以及热变性,在低结合比(r小于0.1 - 0.2)下研究了各种铂配位络合物与核小体和染色质的相互作用。这些物理化学性质变化的总体趋势与DNA - 铂络合物所观察到的相似,这表明铂与DNA及其核蛋白复合物相互作用涉及相同的结合位点。顺式双齿配体,顺式二氯二氨铂、二氨基环己烷和乙二胺铂(II)表现出独特的行为,与反式双齿配体反式二氯二氨铂(II)和单齿配体二亚乙基三胺铂(II)相比,核蛋白中DNA结构的去稳定化更为显著。用这五种配体观察到的碱基在260nm吸收带中负电二色性的急剧下降,表明染色质和核小体中DNA排列发生了深刻变化,这归因于其超螺旋结构的凝聚。与先前关于相同铂化合物的DNA络合物的观察结果存在一些差异,表明在染色质和核小体中可能形成了蛋白质 - DNA交联。这些可能对生物学效应具有一定重要性。