Issue 68, 2014

In vitro investigation of domain specific interactions of phenothiazine dye with serum proteins by spectroscopic and molecular docking approaches

Abstract

In the present study the interaction of the chemotherapeutic agent, Azure A (AZA) with Human Serum Albumin (HSA) and Bovine Serum Albumin (BSA) was investigated by multi spectroscopic and molecular docking methods. The influence of inner filter effect (IFE) on the emission quenching of HSA/BSA at low concentration of AZA (absorption value <0.1) suggested the need to employ an IFE correction factor even for the low concentration regime. The emission titration experiments of HSA/BSA with AZA revealed the formation of AZA–HSA/BSA complexes. The binding parameters calculated from corrected emission intensities showed that AZA binds to HSA/BSA with moderately strong binding affinities. The negative free energy obtained for the binding of AZA with HSA/BSA indicated that the complexation process is spontaneous. The results from site maker competitive experiments with specific site markers revealed that the probable binding location of AZA is located near site I of HSA/BSA. An AutoDock based molecular docking approach was utilized to characterize the binding models of AZA–HSA/BSA complexes. The free energy calculations for the most stable conformer from molecular docking studies were utilized to examine the energy contributions and the role of various amino acid residues of HSA/BSA in AZA binding. The results of site-competitive replacement experiments with specific site markers and molecular docking simulation studies unambiguously helped us to conclude that AZA binds to site I of HSA/BSA. Constant wavelength synchronous emission, excitation–emission matrix (three-dimensional) emission, absorption and circular dichroism spectroscopic techniques have been exploited to unravel AZA induced tertiary and secondary conformational changes of HSA/BSA.

Graphical abstract: In vitro investigation of domain specific interactions of phenothiazine dye with serum proteins by spectroscopic and molecular docking approaches

Article information

Article type
Paper
Submitted
16 Mei 2014
Accepted
06 Ago 2014
First published
06 Ago 2014

RSC Adv., 2014,4, 36267-36281

In vitro investigation of domain specific interactions of phenothiazine dye with serum proteins by spectroscopic and molecular docking approaches

A. S. Sharma, S. Anandakumar and M. Ilanchelian, RSC Adv., 2014, 4, 36267 DOI: 10.1039/C4RA04630G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements