Oxidative DNA cleavage by Schiff base tetraazamacrocyclic oxamido nickel(II) complexes |
| |
Authors: | Kong De-Ming Wang Jiao Zhu Li-Na Jin Ya-Wei Li Xiao-Zeng Shen Han-Xi Mi Huai-Feng |
| |
Affiliation: | Key Laboratory of Functional Polymer Materials (Nankai University), Ministry of Education, Nankai University, Tianjin 300071, PR China. kongdem@nankai.edu.cn |
| |
Abstract: | Nickel is considered a weak carcinogen. Some researches have shown that bound proteins or synthetic ligands may increase the toxic effect of nickel ions. A systematic study of ligand effects on the interaction between nickel complexes and DNA is necessary. Here, we compared the interactions between DNA and six closely related Schiff base tetraazamacrocyclic oxamido nickel(II) complexes NiL(1-3a,1-3b). The structure of one of the six complexes, NiL(3b) has been characterized by single crystal X-ray analysis. All of the complexes can cleave plasmid DNA under physiological conditions in the presence of H(2)O(2). NiL(3b) shows the highest DNA cleavage activity. It can convert supercoiled DNA to nicked DNA then linear DNA in a sequential manner as the complex concentration or reaction time is increased. The cleavage reaction is a typical pseudo-first-order consecutive reaction with the rate constants of 3.27+/-0.14h(-1) (k(1)) and 0.0966+/-0.0042h(-1) (k(2)), respectively, when a complex concentration of 0.6mM is used. The cleavage mechanism between the complex and plasmid DNA is likely to involve hydroxyl radicals as reactive oxygen species. Circular dichronism (CD), fluorescence spectroscopy and gel electrophoresis indicate that the complexes bind to DNA by partial intercalative and groove binding modes, but these binding interactions are not the dominant factor in determining the DNA cleavage abilities of the complexes. |
| |
Keywords: | Schiff base tetraazamacrocyclic oxamido nickel(II) complexes Plasmid DNA Oxidative DNA cleavage Ligands effect Binding mode |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|