Wang Xiao-Yan, Zhang Ji, Li Kun, Jiang Ning, Chen Shan-Yong, Lin Hong-Hui, Huang Yu, Ma Li-Jian, Yu Xiao-Qi
Department of Chemistry, Key Laboratory of Green Chemistry and Technology (Ministry of Education), Sichuan University, Chengdu, 610064, PR China.
Bioorg Med Chem. 2006 Oct 1;14(19):6745-51. doi: 10.1016/j.bmc.2006.05.049. Epub 2006 Jun 22.
Mononuclear macrocyclic polyamine zinc(II), copper(II), cobalt(II) complexes, which could attach to peptide nucleic acid (PNA), were synthesized as DNA cleavage agents. The structures of these new mononuclear complexes were identified by MS and (1)H NMR spectroscopy. The catalytic activities on DNA cleavage of these mononuclear complexes with different central metals were subsequently studied, which showed that copper complex was better catalyst in the DNA cleavage process than zinc and cobalt complexes. The effects of reaction time, concentration of complexes were also investigated. The results indicated that the copper(II) complexes could catalyze the cleavage of supercoiled DNA (pUC 19 plasmid DNA) (Form I) under physiological conditions to produce selectively nicked DNA (Form II, no Form III produced) with high yields. The mechanism of the cleavage process was also studied.
合成了可与肽核酸(PNA)结合的单核大环多胺锌(II)、铜(II)、钴(II)配合物作为DNA切割剂。通过质谱和(1)H核磁共振光谱鉴定了这些新单核配合物的结构。随后研究了这些具有不同中心金属的单核配合物对DNA切割的催化活性,结果表明铜配合物在DNA切割过程中比锌和钴配合物是更好的催化剂。还研究了反应时间、配合物浓度的影响。结果表明,铜(II)配合物在生理条件下可催化超螺旋DNA(pUC 19质粒DNA)(形式I)的切割,以高产率选择性地产生带切口的DNA(形式II,不产生形式III)。还研究了切割过程的机制。