Chen Lan-Mei, Liu Jie, Chen Jin-Can, Tan Cai-Ping, Shi Shuo, Zheng Kang-Cheng, Ji Liang-Nian
Key Laboratory of Bioinorganic and Synthetic Chemistry of the Ministry of Education, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, PR China.
J Inorg Biochem. 2008 Feb;102(2):330-41. doi: 10.1016/j.jinorgbio.2007.09.006. Epub 2007 Oct 1.
Two new Ru(II) complexes Ru(L)(4)(dppz) (L=imidazole (Im), 1-methylimidazole (MeIm); dppz=dipyrido[3,2-a:2',3'-c]phenazine), have been synthesized and characterized in detail by elemental analysis, (1)H NMR, Electrospray ionization mass spectrometry (ESI-MS) and UV-visible (UV-Vis) spectroscopic techniques. The interaction of these complexes with calf thymus DNA (CT-DNA) has been explored by using electronic absorption titration, competitive binding experiment, circular dichroism (CD), thermal denaturation and viscosity measurements. The experimental results show that: both the two complexes can bind to DNA in an intercalation mode; the DNA-binding affinity of complex Ru(Im)(4)(dppz)1 (K(b)=2.5 x 10(6)M(-1)) is greater than that of complex Ru(MeIm)(4)(dppz)2 (K(b)=1.1 x 10(6)M(-1)). Moreover, it is very interesting to find that the circular dichroic spectrum of DNA-complex 1 adduct, in which both bands centered at 277 nm and 236 nm are all negative, is very different from those of DNA-complex 2 adduct and other Ru(II) complexes binding to DNA in general intercalation mode. It may be due to the hydrogen-bonding effect or the contribution of induced CD signals of complex 1. Another interesting finding is that the hypochromism of the complexes is not linear relation to their DNA-binding affinities. In order to deeply study these experimental phenomena and trends, the density functional theory (DFT) and time-dependent DFT (TDDFT) computations were carried out, and on the basis of the DFT/TDDFT results and the frontier molecular orbital theory, the trend in DNA-binding affinities, the spectral properties as well as the interesting phenomena of larger extent of hypochromism but relatively smaller K(b) values for the title complexes have been reasonably explained.
合成了两种新型钌(II)配合物[Ru(L)₄(dppz)]²⁺(L = 咪唑(Im),1 - 甲基咪唑(MeIm);dppz = 二吡啶并[3,2 - a:2',3' - c]吩嗪),并通过元素分析、¹H NMR、电喷雾电离质谱(ESI - MS)和紫外可见(UV - Vis)光谱技术对其进行了详细表征。利用电子吸收滴定、竞争结合实验、圆二色性(CD)、热变性和粘度测量等方法研究了这些配合物与小牛胸腺DNA(CT - DNA)的相互作用。实验结果表明:这两种配合物均能以插入模式与DNA结合;配合物[Ru(Im)₄(dppz)]²⁺ 1(Kb = 2.5×10⁶ M⁻¹)与DNA的结合亲和力大于配合物[Ru(MeIm)₄(dppz)]²⁺ 2(Kb = 1.1×10⁶ M⁻¹)。此外,有趣的是发现DNA - 配合物1加合物的圆二色光谱,其在277 nm和236 nm处的两条谱带均为负,与DNA - 配合物2加合物以及其他以一般插入模式与DNA结合的钌(II)配合物的圆二色光谱有很大不同。这可能是由于氢键效应或配合物1诱导CD信号的贡献。另一个有趣的发现是配合物的减色现象与其DNA结合亲和力并非线性关系。为了深入研究这些实验现象和趋势,进行了密度泛函理论(DFT)和含时密度泛函理论(TDDFT)计算,并基于DFT/TDDFT结果和前沿分子轨道理论,对标题配合物的DNA结合亲和力趋势、光谱性质以及减色程度较大但Kb值相对较小的有趣现象进行了合理的解释。