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Bovine serum albumin interaction, molecular docking, anticancer and antimicrobial activities of Co(II) Schiff base complex derived from Nophen ligand

Jyoti Rani, A. Mary Imelda Jayaseeli, Murugesan Sankarganesh, R. Nandini Asha

2022Journal of Biomolecular Structure and Dynamics23 citationsDOI

Abstract

In this report, synthesis, characterization, biological and molecular modeling studies of Nophen Schiff base [N,N-bis(2-hydroxy-1-naphthaldehyde)-o-phenylenediamine] and Co(II)-Nophen complex have been furnished. BSA binding affinities of the ligand and Co(II)-Nophen complex have been appraised by UV-visible, fluorescence and cyclic voltammetric techniques. Spectroscopic measurements indicate strong binding of the complex with BSA protein through static quenching mechanism with binding constant in the order of 104 M−1. The negative shift of the peak potential in cyclic voltammetry suggested an electrostatic interaction. Molecular docking analysis reveals significant binding affinity (-6.3 kcal/mol) of the complex towards BSA protein. It is amazing that the in vitro cytotoxicity of Co(II)-Nophen complex against A549 cell lines (Human lung carcinoma cells) has remarkable potentials with 29 ± 1.2 µM as IC50 value. Comparing the biological activity towards microorganisms, Co(II)-Nophen complex show substantial response than the Nophen ligand.Communicated by Ramaswamy H. Sarma

Topics & Concepts

Bovine serum albuminSchiff baseChemistryBinding constantLigand (biochemistry)Human serum albuminCytotoxicityDocking (animal)Cyclic voltammetryStereochemistryQuenching (fluorescence)Molecular modelBinding siteFluorescenceIn vitroCombinatorial chemistryBiochemistryElectrochemistryReceptorPhysical chemistryElectrodeQuantum mechanicsNursingPhysicsMedicineMetal complexes synthesis and propertiesProtein Interaction Studies and Fluorescence AnalysisCrystal structures of chemical compounds