DNA/protein interaction and cytotoxic activity of imidazole terpyridine derived Cu(II)/Zn(II) metal complexes

被引:72
作者
Manikandamathavan, V. M. [1 ]
Weyhermueller, T. [2 ]
Parameswari, R. P. [3 ]
Sathishkumar, M. [1 ]
Subramanian, V. [1 ]
Nair, Balachandran Unni [1 ]
机构
[1] CSIR, Cent Leather Res Inst, Chem Lab, Madras 600020, Tamil Nadu, India
[2] Max Planck Inst Bioanorgan Chem, D-45470 Mulheim, Germany
[3] Sri Ramachandra Univ, Dept Biochem, Herbal & Indian Med Res Lab, Madras 600116, Tamil Nadu, India
关键词
DNA-BINDING; ANTIPROLIFERATIVE ACTIVITY; COORDINATION-COMPLEXES; COPPER(II) COMPLEX; DRUG-BINDING; PLATINUM; LIGANDS; CISPLATIN; CLEAVAGE; CELLS;
D O I
10.1039/c4dt01378f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two imidazole terpyridine (itpy) based complexes, [Cu(itpy)(OAc)(H2O)]NO3 center dot H2O (1) and [Zn(itpy)(OAc)]-OAc (2) have been synthesised and characterized. The crystal structure of complex 1 shows distorted octahedral geometry with an anti-parallel stacking arrangement. The interactions of the two complexes with Calf thymus DNA (ctDNA) have been studied using absorption titration and circular dichroism. Complex 1 shows coordinate binding to DNA bases, and complex 2 shows an intercalative mode of binding with DNA. Complex 1 cleaves the DNA via an oxidative pathway in the presence of additives, because of the presence of a redox active copper(II) centre. However, complex 2 cleaves DNA hydrolytically. Interactions of the two complexes with bovine serum albumin have been studied using fluorescence quenching and circular dichroism experiments. Circular dichroic analysis reveals that both the complexes strongly influence the secondary structure of the protein. Fluorescence quenching experiments indicate that there are different binding sites for complexes 1 and 2 on the protein. Furthermore, the complexes show potential cytotoxicity towards the A549 lung cancer cell line. Both the complexes have been found to induce apoptosis.
引用
收藏
页码:13018 / 13031
页数:14
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