Synthesis and characterization of new transition metal {Cu(II), Ni(II) and Co(II)} L-phenylalanine-DACH conjugate complexes: In vitro DNA binding, cleavage and molecular docking studies

被引:55
作者
Shamsi, Manal [1 ]
Yadav, Shipra [1 ]
Arjmand, Farukh [1 ]
机构
[1] Aligarh Muslim Univ, Dept Chem, Aligarh 202002, Uttar Pradesh, India
关键词
Cu(II)-DACH conjugate complex; CT DNA binding studies; Thermal denaturation; pBR322 plasmid cleavage; Topo-I inhibition; TOPOISOMERASE-II; COPPER(II) COMPLEXES; NICKEL(II) COMPLEXES; CANCER-CHEMOTHERAPY; BIOLOGICAL-ACTIVITY; CRYSTAL-STRUCTURE; LIGANDS; CYTOTOXICITY; FLUORESCENCE; INHIBITORS;
D O I
10.1016/j.jphotobiol.2014.04.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The novel metal-based molecular entities {Cu(II), Ni(II) and Co(II)} 1-3, respectively were synthesized and characterized by elemental analysis and spectroscopic methods (IR, H-1 and C-13 NMR, EPR, UV-vis, ESI-MS and XRPD). The interaction studies of 1-3 with CF DNA have been investigated by UV-vis titrations, fluorescence and circular dichroic studies which revealed the electrostatic mode of binding and on the basis of intrinsic binding constant K-b (5.30 x 10(4), 1; 3.41 x 10(4), 2; and 2.74 x 10(4), 3; M-1), the extent of DNA binding was ascertained, following the order 1 > 2 > 3. Specifically, 1 exhibited greater binding propensity with CT DNA, therefore the cleavage activity of 1 with pBR322 DNA was evaluated by agarose gel electrophoresis assay. Complex 1 presented an impressive nuclease activity generating single- and double-strand breaks. Further mechanistic investigation revealed the efficiency of 1 to cleave DNA strands by an oxidative pathway involving the generation of ROS and preferential selectivity towards the DNA minor groove. Moreover, complex 1 exhibited significant inhibitory effects on the catalytic activity of topoisomerase I at a very low concentration similar to 20 mu M. Additionally, computer-aided molecular docking techniques were carried out to correlate and rationalize the observed binding affinities with docking studies towards the molecular target DNA and Topo-I. (C) 2014 Elsevier B.V. All rights reserved.
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页码:1 / 11
页数:11
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