The influence of the flavonoid quercetin on the interaction of propranolol with human serum albumin: Experimental and theoretical approaches

被引:35
|
作者
Mohseni-Shahri, Fatemeh S. [1 ]
Housaindokht, Mohammad R. [1 ]
Bozorgmehr, Mohammad R. [2 ]
Moosavi-Movahedi, Ali A. [3 ]
机构
[1] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad, Iran
[2] Islamic Azad Univ, Mashhad Branch, Dept Chem, Mashhad, Iran
[3] Univ Tehran, Inst Biochem & Biophys, Tehran, Iran
关键词
Fluorescence quenching; Conformational change; Secondary structure; Binding site; Binding constant; RESONANCE LIGHT-SCATTERING; HUMAN HOLO-TRANSFERRIN; MOLECULAR-DYNAMICS; CIRCULAR-DICHROISM; PROTEIN-STRUCTURE; BINDING; INSIGHTS; DOCKING; SPECTROSCOPY; EQUILIBRIUM;
D O I
10.1016/j.jlumin.2014.04.033
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The binding of propranolol (PROP) to human serum albumin (HSA) in the absence and presence of quercetin (QUER) in aqueous solution was investigated by multiple techniques. The presence of quercetin (QUER) increased binding constant of propranolol (PROP) with HSA. Fluorescence spectroscopy showed that quercetin (QUER) could quench the HSA fluorescence spectra. The results of synchronous fluorescence, resonance light scattering (RLS) and three-dimensional fluorescence spectra showed that propranolol (PROP) and quercetin (QUER) would alter the micro-environment around tryptophan (Trp) and tyrosine (Tyr) residues. According molecular dynamics (MD) simulation results suggested that these ligands can interact with the protein, with affecting the secondary structure of HSA and with a modification of its tertiary structure. Molecular docking studies showed that the affinity and binding site of each of the ligands to HSA altered in the presence of the other. All above results may have related consequence in rationalizing the interferences of ordinary food to cardiac dysrhythmias treatments. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 240
页数:12
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