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A small protein probe for correlated microscopy of endogenous proteins

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...

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Autores principales: de Beer, Marit A., Kuipers, Jeroen, van Bergen en Henegouwen, Paul M. P., Giepmans, Ben N. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816110/
https://www.ncbi.nlm.nih.gov/pubmed/29327239
http://dx.doi.org/10.1007/s00418-018-1632-6
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author de Beer, Marit A.
Kuipers, Jeroen
van Bergen en Henegouwen, Paul M. P.
Giepmans, Ben N. G.
author_facet de Beer, Marit A.
Kuipers, Jeroen
van Bergen en Henegouwen, Paul M. P.
Giepmans, Ben N. G.
author_sort de Beer, Marit A.
collection PubMed
description 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00418-018-1632-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-58161102018-02-27 A small protein probe for correlated microscopy of endogenous proteins de Beer, Marit A. Kuipers, Jeroen van Bergen en Henegouwen, Paul M. P. Giepmans, Ben N. G. Histochem Cell Biol Original Paper 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00418-018-1632-6) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-01-11 2018 /pmc/articles/PMC5816110/ /pubmed/29327239 http://dx.doi.org/10.1007/s00418-018-1632-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
de Beer, Marit A.
Kuipers, Jeroen
van Bergen en Henegouwen, Paul M. P.
Giepmans, Ben N. G.
A small protein probe for correlated microscopy of endogenous proteins
title A small protein probe for correlated microscopy of endogenous proteins
title_full A small protein probe for correlated microscopy of endogenous proteins
title_fullStr A small protein probe for correlated microscopy of endogenous proteins
title_full_unstemmed A small protein probe for correlated microscopy of endogenous proteins
title_short A small protein probe for correlated microscopy of endogenous proteins
title_sort small protein probe for correlated microscopy of endogenous proteins
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816110/
https://www.ncbi.nlm.nih.gov/pubmed/29327239
http://dx.doi.org/10.1007/s00418-018-1632-6
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