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一种用于内源性蛋白质相关显微镜检查的小型蛋白质探针。

A small protein probe for correlated microscopy of endogenous proteins.

作者信息

de Beer Marit A, Kuipers Jeroen, van Bergen En Henegouwen Paul M P, Giepmans Ben N G

机构信息

Department of Cell Biology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Division of Cell Biology, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands.

出版信息

Histochem Cell Biol. 2018 Mar;149(3):261-268. doi: 10.1007/s00418-018-1632-6. Epub 2018 Jan 11.

Abstract

Probes are essential to visualize proteins in their cellular environment, both using light microscopy as well as electron microscopy (EM). Correlated light microscopy and electron microscopy (CLEM) requires probes that can be imaged simultaneously by both optical and electron-dense signals. Existing combinatorial probes often have impaired efficiency, need ectopic expression as a fusion protein, or do not target endogenous proteins. Here, we present FLIPPER-bodies to label endogenous proteins for CLEM. Fluorescent Indicator and Peroxidase for Precipitation with EM Resolution (FLIPPER), the combination of a fluorescent protein and a peroxidase, is fused to a nanobody against a target of interest. The modular nature of these probes allows an easy exchange of components to change its target or color. A general FLIPPER-body targeting GFP highlights histone2B-GFP both in fluorescence and in EM. Similarly, endogenous EGF receptors and HER2 are visualized at nm-scale resolution in ultrastructural context. The small and flexible FLIPPER-body outperforms IgG-based immuno-labeling, likely by better reaching the epitopes. Given the modular domains and possibilities of nanobody generation for other targets, FLIPPER-bodies have high potential to become a universal tool to identify proteins in immuno-CLEM with increased sensitivity compared to current approaches.

摘要

无论是使用光学显微镜还是电子显微镜(EM),探针对于在细胞环境中可视化蛋白质都至关重要。相关光显微镜和电子显微镜(CLEM)需要能够通过光学信号和电子致密信号同时成像的探针。现有的组合探针通常效率受损,需要作为融合蛋白进行异位表达,或者不能靶向内源性蛋白质。在这里,我们展示了用于CLEM标记内源性蛋白质的FLIPPER体。用于EM分辨率沉淀的荧光指示剂和过氧化物酶(FLIPPER),即荧光蛋白和过氧化物酶的组合,与针对感兴趣靶标的纳米抗体融合。这些探针的模块化性质允许轻松交换组件以改变其靶标或颜色。一种靶向GFP的通用FLIPPER体在荧光和EM中均突出显示了组蛋白2B-GFP。同样,内源性表皮生长因子受体和HER2在超微结构背景下以纳米级分辨率可视化。小而灵活的FLIPPER体优于基于IgG的免疫标记,可能是因为能更好地接近表位。鉴于纳米抗体生成针对其他靶标的模块化结构域和可能性,与当前方法相比,FLIPPER体有很大潜力成为一种通用工具,以更高的灵敏度在免疫CLEM中鉴定蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c8/5816110/4ab82dcb34df/418_2018_1632_Fig1_HTML.jpg

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