Title of article :
Interaction of Novel Ni2+, Cu2+ and VO2+ Complexes of a Tridentate Schiff Base Ligand with DNA, BSA and their Cytotoxic Activity
Author/Authors :
Dostani, M Nanotechnology Research Center - Bu-Ali Research Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Kianfar, A.H Nanotechnology Research Center - Bu-Ali Research Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Farrokhpour, H Nanotechnology Research Center - Bu-Ali Research Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Abyar, F Nanotechnology Research Center - Bu-Ali Research Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Momtazi-Borojeni, A.A Nanotechnology Research Center - Bu-Ali Research Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Abdollahi, E Department of Medical Immunology - Student Research Committee - Faculty of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
In this research, the interaction of [CuL(DMF)], [NiL(DMF)] and [VOL(DMF)] (where L = ((E)-4-((2-amino-5-
nitrophenylimino)methyl)benzene-1,3-diol)) complexes derived from tridentate Schiff base ligand with bovine serum albumin (BSA) and
DNA was investigated via electronic absorption and fluorescence spectroscopy. The Ultraviolet-Visible (UV-Vis) spectra exhibited an
isosbestic point for the complexes through titration with DNA. The experimental results showed the presence of intercalation interaction
between the complexes and calf-thymus DNA (CT-DNA). The interaction of BSA protein and complexes was significant. The recorded
florescence spectra of complexes interacting with DNA and BSA revealed the static quenching manner. The free binding energies of
complexes and their interaction modes with DNA and BSA were determined by the molecular docking. MTT-dye reduction technique was
applied to define cytotoxicity of [NiL(DMF)], [CuL(DMF)] and [VOL(DMF)] complexes against breast cancer 4T1 and colon carcinoma
C26 cell lines. The [VOL(DMF)] complex had cytotoxic activity against 4T1 and C26 cell lines.
Keywords :
BSA theoretical studies , DNA , Fluorescence spectroscopy , UV-Vis absorption spectroscopy , CT-DNA