Université de Lorraine - Nancy and Centre National de la Recherche Scientifique, Theory-Simulation-Modeling, SRSMC Nancy, France.
Université de Lorraine - Nancy and Centre National de la Recherche Scientifique, Hécrin, SRSMC Nancy, France.
Front Chem. 2015 Dec 18;3:67. doi: 10.3389/fchem.2015.00067. eCollection 2015.
We report the characterization of the interaction between B-DNA and three terpyridin iron II complexes. Relatively long time-scale molecular dynamics (MD) is used in order to characterize the stable interaction modes. By means of molecular modeling and UV-vis spectroscopy, we prove that they may lead to stable interactions with the DNA duplex. Furthermore, the presence of larger π-conjugated moieties also leads to the appearance of intercalation binding mode. Non-covalent stabilizing interactions between the iron complexes and the DNA are also characterized and evidenced by the analysis of the gradient of the electronic density. Finally, the structural deformations induced on the DNA in the different binding modes are also evidenced. The synthesis and chemical characterization of the three complexes is reported, as well as their absorption spectra in presence of DNA duplexes to prove the interaction with DNA. Finally, their effects on human cell cultures have also been evidenced to further enlighten their biological effects.
我们报告了 B-DNA 与三种三吡啶铁 II 配合物之间相互作用的特征。相对较长的时间尺度分子动力学(MD)用于表征稳定的相互作用模式。通过分子建模和紫外可见光谱,我们证明它们可能与 DNA 双链形成稳定的相互作用。此外,较大的π共轭部分的存在也导致了嵌入结合模式的出现。通过电子密度梯度的分析,还对铁配合物与 DNA 之间的非共价稳定相互作用进行了表征和证实。最后,还证明了不同结合模式下 DNA 所诱导的结构变形。报道了三种配合物的合成和化学特性,以及它们在 DNA 双链存在下的吸收光谱,以证明与 DNA 的相互作用。最后,还证明了它们对人细胞培养物的影响,以进一步阐明它们的生物学效应。