The chemical biology of Cu(II) complexes with imidazole or thiazole containing ligands: Synthesis, crystal structures and comparative biological activity

被引:28
作者
Lewis, Adam [1 ]
McDonald, Molly [1 ]
Scharbach, Stephanie [1 ]
Hamaway, Stefan [1 ]
Plooster, Melissa [2 ]
Peters, Kyle [2 ]
Fox, Kristin M. [1 ]
Cassimeris, Lynne [2 ]
Tanski, Joseph M. [3 ]
Tyler, Laurie A. [1 ]
机构
[1] Union Coll, Dept Chem & Biochem, Schenectady, NY 12308 USA
[2] Lehigh Univ, Dept Biol Sci, Bethlehem, PA 18015 USA
[3] Vassar Coll, Dept Chem, Poughkeepsie, NY 12604 USA
关键词
Benzimidazole; Benzothiazole; Copper(II); Nuclease; DNA; Antibacterial; CANCER-CELL LINES; COPPER(II) COMPLEXES; DNA-BINDING; ANTICANCER ACTIVITY; NUCLEASE ACTIVITY; BSA-BINDING; CLEAVAGE; CYTOTOXICITY; BIOSYNTHESIS; ETHIDIUM;
D O I
10.1016/j.jinorgbio.2016.01.014
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 synthesis and characterization of two copper(II) complexes containing 2-(2-pyridyl)benzimidazole (PyBIm) are reported with the biological activity of these two complexes and a third Cu(II) complex containing 2-(2-pyridyl)benzothiazole (PyBTh). Complex 1, [Cu(PyBIm)(NO3)(H2O)](NO3), is a four coordinate, distorted square planar species with one ligand (N,N), nitrate and water bound to Cu(II). The [Cu(PyBIm)(3)](BF4)(2) complex (2) has distorted octahedral geometry with a 3:1 Py(BIm) ligand to metal ratio. The distorted trigonal bi-pyramidal geometry of compound 3, [Cu(PyBTh)(2)(H2O)](BF4)(2), is comprised of two PyBTh ligands and one water. Biological activity of 1-3 has been assessed by analyzing DNA interaction, nuclease ability, cytotoxic activity and antibacterial properties. Complex 3 exhibits potent concentration dependent SC-DNA cleavage forming single- and double-nicked DNA in contrast to the weak activity of complexes 1 and 2. Mechanistic studies indicate that all complexes utilize an oxidative mechanism however 1 and 2 employ O-2(-) as the principal reactive oxygen species while the highly active 3 utilizes O-1(2). The interaction between 1-3 and DNA was investigated using fluorescence emission spectroscopy and revealed all complexes strongly intercalate DNA with K-app values of 2.65 x 10(6), 1.85 x 10(6) and 2.72 x 10(6) M-1, respectively. Cytotoxic effects of 1-3 were examined using HeLa and K562 cells and show cell death in the micromolar range with the activity of 1 approximate to 2 and were slightly higher than 3. Similar reactivity was observed in the antibacterial studies with E. coli and S. aureus. A detailed comparative analysis of the three complexes is presented. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:52 / 61
页数:10
相关论文
共 63 条
[51]   Ternary Dinuclear Copper(II) Complexes of a Hydroxybenzamide Ligand with Diimine Coligands: the 5,6-dmp Ligand Enhances DNA Binding and Cleavage and Induces Apoptosis [J].
Ramakrishnan, Sethu ;
Shakthipriya, Dhanasekaran ;
Suresh, Eringathodi ;
Periasamy, Vaiyapuri Subbarayan ;
Akbarsha, Mohammad Abdulkader ;
Palaniandavar, Mallayan .
INORGANIC CHEMISTRY, 2011, 50 (14) :6458-6471
[52]   Mixed chelate copper complex, Casiopeina IIgly®, binds and degrades nucleic acids:: A mechanism of cytotoxicity [J].
Rivero-Muller, Adolfo ;
De Vizcaya-Ruiz, Andrea ;
Plant, Nick ;
Ruiz, Lena ;
Dobrota, Miloslav .
CHEMICO-BIOLOGICAL INTERACTIONS, 2007, 165 (03) :189-199
[53]   Solution structure of the antitumor candidate trunkamide A by 2D NMR and restrained simulated annealing methods [J].
Salvatella , X ;
Caba, JM ;
Albericio, F ;
Giralt, E .
JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (02) :211-215
[54]   Advances in Copper Complexes as Anticancer Agents [J].
Santini, Carlo ;
Pellei, Maura ;
Gandin, Valentina ;
Porchia, Marina ;
Tisato, Francesco ;
Marzano, Cristina .
CHEMICAL REVIEWS, 2014, 114 (01) :815-862
[55]   A short history of SHELX [J].
Sheldrick, George M. .
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2008, 64 :112-122
[56]  
SIGMAN DS, 1979, J BIOL CHEM, V254, P2269
[57]   Synthesis, characterization, crystal structures and biological activity of set of Cu(II) benzothiazole complexes: Artificial nucleases with cytotoxic activities [J].
Steiner, Ramsey A. ;
Foreman, David ;
Lin, Han X. ;
Carney, Bruce K. ;
Fox, Kristin M. ;
Cassimeris, Lynne ;
Tanski, Joseph M. ;
Tyler, Laurie A. .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2014, 137 :1-11
[58]   Synthesis and characterization of Cu(II)-based anticancer chemotherapeutic agent targeting topoisomerase Iα: In vitro DNA binding, pBR322 cleavage, molecular docking studies and cytotoxicity against human cancer cell lines [J].
Tabassum, Sartaj ;
Zaki, Mehvash ;
Afzal, Mohd. ;
Arjmand, Farukh .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 74 :509-523
[59]   Thioamido coordination in a thioxo-1,2,4-triazole copper(II) complex enhances nonapoptotic programmed cell death associated with copper accumulation and oxidative stress in human cancer cells [J].
Tardito, Saverio ;
Bussolati, Ovidio ;
Maffini, Monica ;
Tegoni, Matteo ;
Giannetto, Marco ;
Dall'Asta, Valeria ;
Franchi-Gazzola, Renata ;
Lanfranchi, Maurizio ;
Pellinghelli, Maria Angela ;
Mucchino, Claudio ;
Mori, Giovanni ;
Marchio, Luciano .
JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (08) :1916-1924
[60]   Copper Compounds in Anticancer Strategies [J].
Tardito, Saverio ;
Marchio, Luciano .
CURRENT MEDICINAL CHEMISTRY, 2009, 16 (11) :1325-1348