DNA cleavage mechanism by metal complexes of Cu(II), Zn(II) and VO(IV) with a schiff-base ligand

被引:36
作者
Rodriguez, Maria R. [1 ]
Lavecchia, Martin J. [1 ]
Parajon-Costa, Beatriz S. [1 ]
Gonzalez-Baro, Ana C. [1 ]
Gonzalez-Baro, Maria R. [2 ]
Cattaneo, Elizabeth R. [2 ]
机构
[1] Univ Nacl La Plata, CEQUINOR Ctr Quim Inorgan Prof Dr Pedro J Aymonin, Consejo Nacl Invest Cient & Tecn CCT La Plata, Bvd 120 N 1469, La Plata, Argentina
[2] Univ Nacl La Plata, INIBIOLP Inst Invest Bioquim La Plata Rodolfo R B, Consejo Nacl Invest Cient & Tecn, Fac Ciencias Med, 60 & 120 S-N, La Plata, Buenos Aires, Argentina
关键词
Schiff bases; Transition metal complexes; DNA binding Studies; Gel electrophoresis; COPPER(II) COMPLEXES; POTENTIAL ANTITUMOR; CRYSTAL-STRUCTURE; FREE-ENERGY; O-VANILLIN; BINDING; VISUALIZATION; CYTOTOXICITY; DYNAMICS; SOLVENT;
D O I
10.1016/j.biochi.2021.04.002
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
Metal ions and metal complexes are important components of nucleic acid biochemistry, participating both in regulation of gene expression and as therapeutic agents. Three new transition metal complexes of copper(II), zinc(II) and oxidovanadium(IV) with a ligand derived from o-vanillin and thiophene were previously synthesized and their antitumor properties were studied in our laboratory. To elucidate some molecular mechanisms tending to explain the cytotoxic effects observed over tumor cells, we investigated the interaction of these complexes with DNA by gel electrophoresis, UV-Vis spectroscopy, docking studies and molecular dynamics simulations. Our spectroscopy and computational results have shown that all of them were able to bind to DNA, Cu(II) complex is located in the minor groove while Zn(II) and oxidovanadium(IV) complexes act as major groove binding molecules. Interestingly, only the Cu(II) complex caused double-strand DNA nicks, consistent with its higher cytotoxic activities previously observed in tumor cell lines. We propose that the DNA-complex interaction destabilize the molecule either disrupting the phosphodiester bonds or impairing DNA replication, giving those complexes strong antitumor potential. (c) 2021 Elsevier B.V. and Soci & eacute;t & eacute; Fran & ccedil;aise de Biochimie et Biologie Mol & eacute;culaire (SFBBM). All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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