Krivtsova M A, Moroshkina E B, Khamman Kh, Glibin E N, Frisman E V
Mol Biol (Mosk). 1981 May-Jun;15(3):613-21.
The DNA complexes with actinomycin D and its simple analogues have been investigated by means of spectrophotometry, viscometry and flow birefringence methods. The number of binding sites per base pair of ligand on DNA depends on the nature of substitute in 1.9 position of the phenoxasone chromophore. It has been shown that phenoxasone derivatives without aminogroup in 2 position complex with DNA as in the case of simple actinomycin analogues. The intrinsic viscosity and optical anisotropy of DNA-analogues complexes increase linerly with increasing quantity of bound ligand. This testifies that the binding of the compounds under investigation to DNA molecule is of intercalation type. The character of variation of hydrodynamical and optical parameters of DNA molecule by its binding with actinomycin differs qualitatively from that observed by the binding with analogues. The experimental data obtained for DNA-actinomycin complexes can be interpreted only by suggesting a specific secondary structure alteration of the DNA molecule. It has been shown that the simple actinomycin analogues can not be used as an appropriate model for investigation of DNA-actinomycin complexes structure.
已通过分光光度法、粘度测定法和流动双折射法对与放线菌素D及其简单类似物形成的DNA复合物进行了研究。配体在DNA上每碱基对的结合位点数取决于吩恶嗪发色团1.9位取代基的性质。已表明,2位无氨基的吩恶嗪衍生物与DNA形成复合物的情况与简单放线菌素类似物相同。DNA - 类似物复合物的特性粘度和光学各向异性随结合配体数量的增加呈线性增加。这证明所研究的化合物与DNA分子的结合属于嵌入型。DNA分子通过与放线菌素结合而导致的流体动力学和光学参数变化的特征,与通过与类似物结合所观察到的情况在性质上有所不同。所获得的关于DNA - 放线菌素复合物的实验数据,只有通过假定DNA分子特定的二级结构改变才能得到解释。已表明,简单的放线菌素类似物不能用作研究DNA - 放线菌素复合物结构的合适模型。