郭明, 谭贤, 王莹, 高小艳, 伍周玲, 张丽君. 黄芩苷-金属配合物与血清蛋白的分子作用机制研究J. 药学学报, 2015,50(5): 613-620.
引用本文: 郭明, 谭贤, 王莹, 高小艳, 伍周玲, 张丽君. 黄芩苷-金属配合物与血清蛋白的分子作用机制研究J. 药学学报, 2015,50(5): 613-620.
GUO Ming, TAN Xian, WANG Ying, GAO Xiao-yan, WU Zhou-ling, ZHANG Li-jun. The molecular mechanism between baicalin metal complexes and bovin serum albumJ. Acta Pharmaceutica Sinica, 2015,50(5): 613-620.
Citation: GUO Ming, TAN Xian, WANG Ying, GAO Xiao-yan, WU Zhou-ling, ZHANG Li-jun. The molecular mechanism between baicalin metal complexes and bovin serum albumJ. Acta Pharmaceutica Sinica, 2015,50(5): 613-620.

黄芩苷-金属配合物与血清蛋白的分子作用机制研究

The molecular mechanism between baicalin metal complexes and bovin serum album

  • 摘要: 制备新型碳纳米管修饰玻碳电极 (F-CNTs/GCE), 建立F-CNTs/GCE分析黄芩苷-金属配合物 (baicalin metal complexes, BMC) 与血清蛋白 (bovin serum album, BSA) 分子作用机制的研究新方法, 并对该方法的原理深入探讨。模拟生理条件下, 应用循环伏安法对BMC与BSA的相互作用性能进行热力学与动力学研究, 推断BSA与BMC的分子作用机制。结果表明, F-CNTs的存在能加速电子传递, F-CNTs/GCE对BMC/BMC-BSA体系表现出较优的响应信号; 利用新方法检测BMC-BSA的相互作用, 表明BMC-BSA生成了热力学稳定非共价化合物, BMC-BSA的平均结合位点数为1.7, BMC/BMC-BSA反应过程的电子转移数为2, 利用该方法推断BMC与BSA二者结合生成了一种非电化学活性的超分子化合物。本研究为药物与蛋白相互作用的分子机制研究提供新思路, 对探讨非共价相互作用具有一定参考。

     

    Abstract: In this paper, the new carbon nanotube modified glassy carbon electrode (F-CNTs/GCE) was prepared to establish a new method for studying the molecular interaction mechanism between baicalin metal complexes (BMC) and bovine serum album (BSA), and the principle of this method was discussed deeply. Under the physiological condition, the thermodynamics and kinetics properties of interaction between BMC and BSA were studied by cyclic voltammetry (CV) to inference their molecular effective mechanism. The results show that the presence of F-CNTs can accelerate the electron transfer, and better response signal was showed in the BMC/BMC-BSA system. The detection of interaction of BMC-BSA used new method show that BMC-BSA generates stable thermodynamically non-covalent compounds, and the obtained average binding sites of BMC- BSA were 1.7; the number of electron transfer in BMC/BMC-BSA reaction process was 2, and non electroactive supramolecular compounds of BMC-BSA were generated by this interacting reaction. The relevant research work provides a new way to study the molecular mechanism for the interaction of drugs with protein, and with a certain reference value for discussion on the non covalent interactions.

     

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