量子点生物偶联物:通过FRET研究蛋白质相互作用和动力学的巨大潜力的新兴工具

E. M. Gálvez, J. Pardo
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引用次数: 6

摘要

基于荧光技术的方法已被广泛应用于分析无细胞系统和完整细胞中的蛋白质功能、动力学、相互作用和折叠。荧光共振能量转移(FRET)是一种独特的技术,可以精确计算蛋白质的分子间和分子内距离,从而研究蛋白质-蛋白质/肽的相互作用、折叠和构象变化。然而,在单分子水平和/或完整细胞中对这些过程进行详细研究,需要具有高稳定性和量子产率的荧光染料。在过去的六年中,荧光纳米晶体(量子点)作为一种强大的、有前途的荧光染料得到了发展,它满足了在FRET基础上研究蛋白质功能的先决条件。本文的目的是总结量子点在生物系统中蛋白质功能和动力学研究中的优点和缺点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantum dot bioconjugates: emerging tools with great potential to study protein interactions and dynamics by FRET
Methods based on fluorescence technology have been widely employed to analyse protein function, dynamics, interactions and folding in cell free systems as well as in intact cells. Fluorescence resonance energy transfer (FRET) is a unique technique to precisely calculate inter- and intra-molecular distances in proteins and thus to study protein-protein/peptide interaction, folding and conformational changes. However detailed studies of these processes at the single molecule level and/or in intact cells, requires fluorescence dyes with high stability and quantum yield. During the last six years fluorescent nanocrystals (quantum dots) have been developed as potent and promising fluorescence dyes that fulfil the prerequisites to study protein function in FRET based assays. It is the aim of this short review to summarise the benefits and drawbacks of QDs in the study of protein function and dynamics in biological systems.
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