Spectroscopic and electrochemical studies on the interaction of an inclusion complex of β-cyclodextrin/fullerene with bovine serum albumin in aqueous solution

被引:10
|
作者
Zhang, Mei-Fang [1 ,2 ]
Fu, Li [1 ,2 ]
Wang, Jia [1 ,2 ]
Xu, Zi-Qiang [1 ,2 ]
Jiang, Feng-Lei [1 ,2 ]
Liu, Yi [1 ,2 ,3 ]
机构
[1] Wuhan Univ, State Key Lab Virol, Minist Educ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Key Lab Analyt Chem Biol & Med, Minist Educ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[3] Xianning Univ, Dept Chem & Life Sci, Xianning 437005, Peoples R China
基金
中国国家自然科学基金;
关键词
Functionalization; Fluorescence spectroscopy; Aqueous solution; (beta-CD)(2)/C-60 complex; Bovine serum albumin; FLUORESCENCE; BINDING; WATER; C-60; THERMODYNAMICS; CONFORMATION; CHEMISTRY;
D O I
10.1016/j.jphotochem.2011.11.009
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
The potential effect of human exposure to carbonaceous nanomaterials (e.g., fullerenes or their derivatives) in the environment has become a concern. In the current study, we report the interaction of one water-soluble fullerene with bovine serum albumin using spectroscopic and electrochemical methods under aqueous solutions. The novel supramolecular inclusion complex of the water-soluble fullerene (beta-CD)(2)/C-60 was synthesized and characterized. In the mechanism discussed, the spectroscopic methods such as fluorescence quenching and ultraviolet-visible absorption, proved that the fluorescence quenching of BSA by (beta-CD)(2)/C-60 was the result of the formation of (beta-CD)(2)/C-60-BSA complex and that the mechanism of quenching might be a static quenching procedure. The binding constants K-a, the number of binding sites n, and the corresponding thermodynamic parameters Delta G, Delta H, and Delta S at different temperatures were calculated through fluorescence spectroscopy, then as an auxiliary method, the electrochemical impedance spectroscopy (EIS) experiments confirmed this conclusion. The results indicated that the electrostatic interactions play a major role in (beta-CD)(2)/C-60-BSA association. The circular dichroism spectra show the conformation change of the effect of (beta-CD)(2)/C-60 on the conformation of BSA, which was confirmed by the results of the three-dimensional fluorescence spectra. Site marker competitive experiments indicate that the binding of (beta-CD)(2)/C-60 to BSA primarily took place in site I. The distance r between donor (BSA) and acceptor ((beta-CD)(2)/C-60) was obtained according to fluorescence resonance energy transfer (FRET). This work aims to demonstrate the mechanisms of the formation of the complex between water-soluble fullerene and protein under physiological conditions, as well as the remediation for the possible unwarranted biological effects of water-soluble fullerene. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 37
页数:10
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