Tan Li-Feng, Liu Xiao-Hua, Chao Hui, Ji Liang-Nian
College of Chemistry, Xiangtan University, Xiangtan 411105, PR China.
J Inorg Biochem. 2007 Jan;101(1):56-63. doi: 10.1016/j.jinorgbio.2006.08.006. Epub 2006 Aug 30.
A new polypyridyl ligand MPPIP {MPPIP=2-(3'-phenoxyphenyl)imidazo[4,5-f]-[1,10]phenanthroline} and its ruthenium(II) complexes, Ru(bpy)(2)MPPIP (1) (bpy=2,2'-bipyridine) and Ru(phen)(2)MPPIP (2) (phen=1,10-phenanthroline) have been synthesized and characterized. The binding of the two complexes to calf thymus DNA (CT-DNA) has been investigated with spectrophotometric methods, viscosity measurements, as well as equilibrium dialysis and circular dichroism spectroscopy. The results suggest that both complexes bind to CT-DNA through intercalation, and enantioselectively interact with CT-DNA in a way. However, complex 2 is a much better candidate as an enantioselective binder to CT-DNA than complex 1. When irradiated at 365nm, both complexes have also been found to promote the photocleavage of plasmid pBR322 DNA.
一种新型的多吡啶配体MPPIP {MPPIP = 2-(3'-苯氧基苯基)咪唑并[4,5-f]-[1,10]菲咯啉}及其钌(II)配合物Ru(bpy)(2)MPPIP (1) (bpy = 2,2'-联吡啶)和Ru(phen)(2)MPPIP (2) (phen = 1,10-菲咯啉)已被合成并表征。采用分光光度法、粘度测量、平衡透析和圆二色光谱法研究了这两种配合物与小牛胸腺DNA (CT-DNA)的结合情况。结果表明,两种配合物均通过插入作用与CT-DNA结合,并以某种方式对CT-DNA进行对映选择性相互作用。然而,配合物2作为CT-DNA的对映选择性结合剂比配合物1更具优势。当在365nm波长下照射时,还发现两种配合物均能促进质粒pBR322 DNA的光裂解。