Water-induced fluorescence turn-on imidazole derivative and its interaction with bovine serum albumin

被引:7
|
作者
Behera, S. [1 ]
Dash, Pragyan P. [1 ]
Mohanty, P. [1 ]
Behura, R. [1 ]
Sahoo, Suban K. [2 ]
Jali, B. R. [1 ]
机构
[1] Veer Surendra Sai Univ Technol, Dept Chem, Sambalpur 768018, Odisha, India
[2] Sardar Vallabhbhai Natl Inst Technol, Dept Chem, Surat 395007, India
关键词
Trityl imidazole; Water sensor; Protein-ligand interaction study; Molecular docking; ELECTRON-TRANSFER SENSOR; TRACE WATER; ANTIINFLAMMATORY ACTIVITIES; BIOACTIVE IMIDAZOLE; BINDING INTERACTION; ORGANIC-SOLVENTS; IN-VIVO; PROTEINS; GOLD; NANOPARTICLES;
D O I
10.1016/j.molstruc.2023.135158
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new trityl imidazole derivative L was synthesized in one-step by reacting 1H-imidazole with triph-enylmethyl chloride. The receptor L was applied for the detection of trace amounts of water in DMSO. The weakly emissive L in DMSO showed a significant fluorescence enhancement upon the addition of water due to the suppression of the photo-induced electron transfer process and aggregation-induced emission. The sensitivity of L to detect water in DMSO was estimated as 0.002 wt%. Further, the protein-ligand binding interaction between L and BSA was explored by steady-state fluorescence, fluorescence anisotropy and fluorescence lifetime under physiological conditions at pH 7. The formation of the BSA-L complex quenched the fluorescence emission of BSA. The molecular docking analysis was performed to establish the binding mode and stability of the BSA-L complex. The multiple non-covalent interactions occurred between the residues of BSA and the receptor L stabilized the BSA-L complex.(c) 2023 Elsevier B.V. All rights reserved.
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页数:12
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