Probing of the binding profile of anti-hypertensive drug, captopril with bovine serum albumin: A detailed calorimetric, spectroscopic and molecular docking studies. (November 2018)

• Record Type: Journal Article
• Authors: Khatun, Samima; Riyazuddeen,
• Is Part Of: Journal of chemical thermodynamics. Volume 126(2018)
• Page Start: 43
• Page End: 53
• Publication Date: 2018-11
• Subjects: Bovine serum albumin -- Captopril -- Isothermal titration calorimetry -- Spectroscopy -- Conformational change -- Molecular docking; Thermodynamics -- Periodicals; Thermochemistry -- Periodicals; Thermodynamique -- Périodiques; Thermochimie -- Périodiques; Thermochemistry; Thermodynamics; Periodicals; 541.369
• DOI: 10.1016/j.jct.2018.06.004
• Languages: English
• ISSNs: 0021-9614

Abstract

Highlights: CAP quenches the fluorescence spectra of BSA in a static manner. ITC shows that BSA-CAP association process is an enthalpically driven process. CAP binds with BSA at site I (sub-domain IIA). CAP stabilized the native structure of BSA revealed by CD spectroscopy. Secondary structure alteration of BSA was studied by synchronous, 3D and FTIR. Abstract: Captopril (CAP), an angiotensin-converting enzyme inhibitor, widely used for the treatment of hypertension. The current study was undertaken to explore the interaction between CAP and the primary plasma protein, bovine serum albumin (BSA) by fluorescence, isothermal titration calorimetry, Förster's resonance energy transfer, circular dichroism, fourier transform infrared and molecular docking studies. The fluorescence result indicated that CAP quenches the fluorescence intensity of native BSA through a static manner with blue shift in wavelength maxima. Thermodynamic analysis from ITC suggested that hydrogen bonding and van der Waals forces play major role in the association process and it is an enthalpically driven process. The distance between donor (BSA) and acceptor (CAP) has been calculated according to FRET theory. The ITC based displacement experiments concluded that CAP primarily bound to near sub-domain IIA (Sudlow's site I) of BSA. Alteration in the secondary structure of BSA by CAP is revealed by CD which is further substantiated by synchronous, 3D fluorescence and FTIR spectroscopy. In addition, molecular docking was performed to further confirm the biophysical methods. This study provides an insight into the molecular basis of interaction between CAP and BSA which helps to understand the activity and mechanism of drug binding to protein.