Biomolecular interaction of a platelet aggregation inhibitor, 3,4-methylenedioxy-beta-nitrostyrene with human serum albumin: Multi-spectral and computational characterization

Kabir, Md Zahirul and Roslan, Amira Adlin and Ridzwan, Nor Farrah Wahidah and Mohamad, Saharuddin and Tayyab, Saad (2020) Biomolecular interaction of a platelet aggregation inhibitor, 3,4-methylenedioxy-beta-nitrostyrene with human serum albumin: Multi-spectral and computational characterization. Journal of Biomolecular Structure and Dynamics, 38 (9). pp. 2693-2703. ISSN 0739-1102, DOI https://doi.org/10.1080/07391102.2019.1640133.

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Abstract

Molecular interaction of the 3,4-methylenedioxy-beta-nitrostyrene (MNS), an inhibitor of platelet aggregation with the main transport protein, albumin from human serum (HSA) was explored using absorption, fluorescence and circular dichroism (CD) spectroscopy in combination with in silico analyses. The MNS-HSA complexation was corroborated from the fluorescence and absorption spectral results. Implication of static quenching mechanism for MNS-HSA system was predicted from the Stern-Volmer constant, K(SV-)temperature relationship as well as the bimolecular quenching rate constant, k(q) values. Stabilization of the complex was affirmed by the value of the binding constant (K-a = 0.56-1.48 x 10(4) M-1). Thermodynamic data revealed that the MNS-HSA association was spontaneously driven mainly through hydrophobic interactions along with van der Waal's interaction and H-bonds. These results were well supported by in silico interpretations. Far-UV and near-UV CD spectral results manifested small variations in the protein's secondary and tertiary structures, respectively, while three-dimensional fluorescence spectra displayed microenvironmental fluctuations around protein's fluorophores, upon MNS binding. Significant improvement in the protein's thermostability was evident from the temperature-stability results of MNS-bound HSA. Binding locus of MNS, as identified by competitive drug displacement findings as well as in silico analysis, was found to be located in subdomain IIA (Sudlow's site I) of the protein. Communicated by Ramaswamy H. Sarma

Item Type: Article
Funders: University of Malaya Frontier Science Research Cluster (FRSC) [Frontier Research Grant (FRG) 2017] (FG025-17AFR)
Uncontrolled Keywords: 3; 4-methylenedioxy-beta-nitrostyrene; Human serum albumin; Ligand-protein interaction; Fluorescence; In silico analysis
Subjects: Q Science > QH Natural history > QH301 Biology
Divisions: Faculty of Science > Institute of Biological Sciences
Depositing User: Ms Zaharah Ramly
Date Deposited: 03 Mar 2023 07:12
Last Modified: 03 Mar 2023 07:12
URI: http://eprints.um.edu.my/id/eprint/37285

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