Zhang Q L, Liu J G, Liu J, Xue G Q, Li H, Liu J Z, Zhou H, Qu L H, Ji L N
The Key Laboratory of Gene Engineering of Ministry of Education and Department of Chemistry, Zhongshan University, Guangzhou 510275, PR China.
J Inorg Biochem. 2001 Jul;85(4):291-6. doi: 10.1016/s0162-0134(01)00212-4.
The ligand 2-(2-chloro-5-nitrophenyl)imidazo[4,5-f][1,10]phenanthroline(CNOIP) and its complexes Co(bpy)(2)(CNOIP) (1) and Co(phen)(2)(CNOIP) (2) (bpy=2,2'-bipyridine; phen=1,10-phenanthroline) have been synthesized and characterized. Binding of the two complexes with calf thymus DNA has been investigated by spectroscopic methods, cyclic voltammetry, viscosity, and electrophoresis measurements. The experimental results indicate that both complexes bind to DNA through an intercalative mode. In comparison with their parent complexes containing PIP ligand (PIP=2-phenylimidazo[4,5-f][1,10]phenanthroline), the introduction of NO(2) and Cl groups to the PIP ligand decreased the binding affinity of complexes 1 and 2 to CT DNA. Both complexes have also been found to promote the photocleavage of plasmid pBR 322 DNA, the hydroxyl radical (OH*) is suggested to be the reactive species responsible for the cleavage.
配体2-(2-氯-5-硝基苯基)咪唑并[4,5-f][1,10]菲咯啉(CNOIP)及其配合物Co(bpy)(2)(CNOIP) (1)和Co(phen)(2)(CNOIP) (2) (bpy = 2,2'-联吡啶;phen = 1,10-菲咯啉)已被合成并表征。通过光谱法、循环伏安法、粘度和电泳测量研究了这两种配合物与小牛胸腺DNA的结合。实验结果表明,两种配合物均通过插入模式与DNA结合。与含有PIP配体(PIP = 2-苯基咪唑并[4,5-f][1,10]菲咯啉)的母体配合物相比,向PIP配体中引入NO(2)和Cl基团降低了配合物1和2与CT DNA的结合亲和力。还发现两种配合物均能促进质粒pBR 322 DNA的光裂解,羟基自由基(OH*)被认为是负责裂解的活性物种。