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当前资源共 2条
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  • 1. ChinaXiv:202306.00209
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    A facile method for studying interaction of rhodamine B and bovine serum albumin: Towards physical-binding mediated fluorescence labeling of proteins

    分类: 物理学 >> 核物理学 提交时间: 2023-06-18 合作期刊: 《Nuclear Science and Techniques》

    MA Yu-Xing ZHONG Rui-Bo GUO Jun LIU Yu-Shuang YUAN Ming BAI Zhi-Jun LIU Tao-Tao ZHAO Xin-Min ZHANG Feng

    摘要: Strategies for labeling proteins with fluorophores are always important for biotechnology. Here we take a model protein (bovine serum albumin) and a typical fluorophore (rhodamine B) to demonstrate a direct labeling method just by physical adsorption. In combination with size exclusion chromatography and the Scartchard equation, we have developed a facile analysis method for calculating the binding constant and binding sites. The molecular docking method has been used to study the binding site in amino acid level.

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  • 2. ChinaXiv:202306.00271
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    Fluorimetric study on the interaction between fluoresceinamine and bovine serum albumin

    分类: 物理学 >> 核物理学 提交时间: 2023-06-18 合作期刊: 《Nuclear Science and Techniques》

    LIU Yu-Shuang ZHANG Ping ZHONG Rui-Bo BAI Zhi-Jun GUO Jun ZHAO Guo-Fen ZHANG Feng

    摘要: Fluorescence spectroscopy was employed to investigate the interaction between fluorophore fluoresceinamine (FA) and bovine serum albumin (BSA) under physiological conditions. In the mechanism discussion, it was proved that the fluorescence quenching of BSA by FA is a result of the formation of a BSA-FA complex. Fluorescence quenching constants were determined using the modified Stern-Volmer equation to provide a measure of the binding affinity between FA and BSA. The results of the thermodynamic parameters G, H, and S at different temperatures indicated that several kinds of interactions, except for the electrostatic interactions play cooperative roles in BSA-FA association. Furthermore, the conformation of BSA upon interaction with FA was also studied by synchrotron fluorescence spectroscopy.

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友情链接 : ChinaXiv PubScholar 哲学社会科学预印本
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