Spectral studies on the interaction between HSSC and apoCopC

被引:9
|
作者
Song, Zhen [1 ]
Wang, Jinglin [1 ]
Yang, Binsheng [1 ]
机构
[1] Shanxi Univ, Minist Educ, Key Lab Chem Biol & Mol Engn, Inst Mol Sci, Taiyuan 030006, Peoples R China
关键词
ApoCopC; HSSC; Fluorescence; BOVINE SERUM-ALBUMIN; PSEUDOMONAS-SYRINGAE; INTERMOLECULAR TRANSFER; COPPER-RESISTANCE; COPC PROTEIN; FLUORESCENCE; BINDING; OXYGEN; THERMODYNAMICS; PROBE;
D O I
10.1016/j.saa.2013.09.025
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The interaction between HSSC (SSC = salicylaldehyde semicarbazone anion) and apoCopC has been investigated in detail by means of UV, fluorescence and fluorescence lifetime measurement in 10 mM Hepes buffer, at pH 7.4, 25 degrees C. The results suggested that HSSC can form a novel supramolecular system with apoCopC, which can form a 1:1 host-guest inclusion supramolecular complex with HSSC, and the forming constant had been calculated to be (8.83 +/- 0.32) x 10(5) M-1. It suggested the strong inclusion ability of apoCopC to the guest molecules. In addition, the stoichiometric ratio of Cu2+ and HSSC was 1:1, which was the same as Cu2+ and apoCopC. However, the binding ability between Cu2+ and HSSC was much weaker than that between Cu2+ and apoCopC. Moreover, the binding ability of HSSC with Cu2+ has an effect on the binding ability between HSSC and apoCopC, and vice versa. The reason attributed to this effect was that the formation of hydrogen bond between Met46 in apoCopC and the phenolic hydroxyl of HSSC participated in the copper coordination. Furthermore, it was also found that HSSC quench the fluorescence of apoCopC by the static quenching process and the number of binding site was calculated. The thermodynamic parameters Delta H degrees, Delta S degrees and Delta G degrees at different temperatures were obtained. The formation of apoCopC-HSSC complex depended on the cooperation of the van der Waals force and hydrogen bond, and the binding average distance between apoCopC and HSSC was determined. What is more, the binding site of HSSC to apoCopC was shown vividly by an automated public domain software package ArgusLab 4.0.1. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:454 / 460
页数:7
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