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活细胞中感兴趣蛋白质的荧光标记:超越荧光蛋白。

Fluorescent Labeling of Proteins of Interest in Live Cells: Beyond Fluorescent Proteins.

机构信息

State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan 430071, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Bioconjug Chem. 2020 Jun 17;31(6):1587-1595. doi: 10.1021/acs.bioconjchem.0c00181. Epub 2020 May 19.

Abstract

Live cell imaging brings us into a new era of direct visualization of biological processes and molecular dynamics in real time. To visualize dynamic cellular processes and virus-host interactions, fluorescent labeling of proteins of interest is often necessary. Fluorescent proteins are widely used for protein imaging, but they have some intrinsic deficiencies such as big size, photobleaching, and spectrum restriction. Thus, a variety of labeling strategies have been established and continuously developed. To protect the natural biological function(s) of the protein of interest, especially in viral life cycle, labeling requires smaller-sized tags, more specificity, and lower cytotoxicity. Here, we briefly summarized the principles, development, and their applications mainly in the virology field of three strategies for fluorescent labeling of proteins of interest including self-labeling enzyme derivatives, stainable peptide tags, and non-canonical amino acid incorporation. These labeling techniques greatly expand the fluorescent labeling toolbox and provide new opportunities for imaging biological processes.

摘要

活细胞成像使我们进入了一个实时直接观察生物过程和分子动力学的新时代。为了可视化动态细胞过程和病毒-宿主相互作用,通常需要对感兴趣的蛋白质进行荧光标记。荧光蛋白被广泛用于蛋白质成像,但它们具有一些内在的缺陷,如体积大、光漂白和光谱限制。因此,已经建立了各种标记策略并不断发展。为了保护感兴趣的蛋白质的天然生物学功能(特别是在病毒生命周期中),标记需要更小的标签、更高的特异性和更低的细胞毒性。在这里,我们简要总结了三种用于感兴趣的蛋白质荧光标记的策略的原理、发展及其主要在病毒学领域的应用,包括自标记酶衍生物、可染色肽标签和非规范氨基酸掺入。这些标记技术极大地扩展了荧光标记工具箱,并为成像生物过程提供了新的机会。

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