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静水压力对 Cy3 标记藻蓝蛋白体系荧光和 FRET 行为的影响。

Hydrostatic pressure effects on the fluorescence and FRET behavior of Cy3-labeled phycocyanin system.

机构信息

State Key Laboratory of Supramolecular Structure and Materials, Jilin University, No. 2699, Qianjin Street, Changchun, 130012, People's Republic of China.

出版信息

J Phys Chem B. 2012 Sep 13;116(36):11010-6. doi: 10.1021/jp306466j. Epub 2012 Sep 4.

Abstract

FRET has been used as a powerful tool in biological fields as biosensors, bioimaging, protein folding/unfolding monitoring, biomolecular interactions, and so on. It is also important to applying FRET to high hydrostatic pressure studies on biosystems or biorelated systems. Herein, we construct a FRET system by labeling Cy3 on C-phycocyanin (C-PC) to investigate the effect of hydrostatic pressure on the fluorescence and FRET behavior between them. The fluorescence spectra of individual Cy3, C-PC, and integrated Cy3/C-PC system are measured separately under compression. An enhanced FRET efficiency under compression is concluded based on fluorescence behavior differences between them. To further reveal the origination of the enhanced FRET efficiency with pressure, the overlap integral between Cy3 emission and C-PC absorption is also calculated, and several possible explanations are proposed.

摘要

荧光能量转移(FRET)已被广泛应用于生物领域,如生物传感器、生物成像、蛋白质折叠/展开监测、生物分子相互作用等。将 FRET 应用于生物体系或生物相关体系的高压研究也非常重要。在此,我们通过将 Cy3 标记在藻蓝蛋白(C-PC)上来构建一个 FRET 系统,以研究静压对它们之间荧光和 FRET 行为的影响。分别在压缩下单独测量单个 Cy3、C-PC 和集成 Cy3/C-PC 系统的荧光光谱。根据它们之间荧光行为的差异,得出了在压缩下增强的 FRET 效率的结论。为了进一步揭示压力下增强的 FRET 效率的起源,还计算了 Cy3 发射与 C-PC 吸收之间的重叠积分,并提出了几种可能的解释。

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