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In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster
Despite remarkable developments in diffraction unlimited super-resolution microscopy, in vivo nanoscopy of tissues and model organisms is still not satisfactorily established and rarely realized. RESOLFT nanoscopy is particularly suited for live cell imaging because it requires relatively low light...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927295/ https://www.ncbi.nlm.nih.gov/pubmed/27355614 http://dx.doi.org/10.7554/eLife.15567 |
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author | Schnorrenberg, Sebastian Grotjohann, Tim Vorbrüggen, Gerd Herzig, Alf Hell, Stefan W Jakobs, Stefan |
author_facet | Schnorrenberg, Sebastian Grotjohann, Tim Vorbrüggen, Gerd Herzig, Alf Hell, Stefan W Jakobs, Stefan |
author_sort | Schnorrenberg, Sebastian |
collection | PubMed |
description | Despite remarkable developments in diffraction unlimited super-resolution microscopy, in vivo nanoscopy of tissues and model organisms is still not satisfactorily established and rarely realized. RESOLFT nanoscopy is particularly suited for live cell imaging because it requires relatively low light levels to overcome the diffraction barrier. Previously, we introduced the reversibly switchable fluorescent protein rsEGFP2, which facilitated fast RESOLFT nanoscopy (Grotjohann et al., 2012). In that study, as in most other nanoscopy studies, only cultivated single cells were analyzed. Here, we report on the use of rsEGFP2 for live-cell RESOLFT nanoscopy of sub-cellular structures of intact Drosophila melanogaster larvae and of resected tissues. We generated flies expressing fusion proteins of alpha-tubulin and rsEGFP2 highlighting the microtubule cytoskeleton in all cells. By focusing through the intact larval cuticle, we achieved lateral resolution of <60 nm. RESOLFT nanoscopy enabled time-lapse recordings comprising 40 images and facilitated recordings 40 µm deep within fly tissues. DOI: http://dx.doi.org/10.7554/eLife.15567.001 |
format | Online Article Text |
id | pubmed-4927295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49272952016-07-01 In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster Schnorrenberg, Sebastian Grotjohann, Tim Vorbrüggen, Gerd Herzig, Alf Hell, Stefan W Jakobs, Stefan eLife Cell Biology Despite remarkable developments in diffraction unlimited super-resolution microscopy, in vivo nanoscopy of tissues and model organisms is still not satisfactorily established and rarely realized. RESOLFT nanoscopy is particularly suited for live cell imaging because it requires relatively low light levels to overcome the diffraction barrier. Previously, we introduced the reversibly switchable fluorescent protein rsEGFP2, which facilitated fast RESOLFT nanoscopy (Grotjohann et al., 2012). In that study, as in most other nanoscopy studies, only cultivated single cells were analyzed. Here, we report on the use of rsEGFP2 for live-cell RESOLFT nanoscopy of sub-cellular structures of intact Drosophila melanogaster larvae and of resected tissues. We generated flies expressing fusion proteins of alpha-tubulin and rsEGFP2 highlighting the microtubule cytoskeleton in all cells. By focusing through the intact larval cuticle, we achieved lateral resolution of <60 nm. RESOLFT nanoscopy enabled time-lapse recordings comprising 40 images and facilitated recordings 40 µm deep within fly tissues. DOI: http://dx.doi.org/10.7554/eLife.15567.001 eLife Sciences Publications, Ltd 2016-06-29 /pmc/articles/PMC4927295/ /pubmed/27355614 http://dx.doi.org/10.7554/eLife.15567 Text en © 2016, Schnorrenberg et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Schnorrenberg, Sebastian Grotjohann, Tim Vorbrüggen, Gerd Herzig, Alf Hell, Stefan W Jakobs, Stefan In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster |
title | In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster |
title_full | In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster |
title_fullStr | In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster |
title_full_unstemmed | In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster |
title_short | In vivo super-resolution RESOLFT microscopy of Drosophila melanogaster |
title_sort | in vivo super-resolution resolft microscopy of drosophila melanogaster |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927295/ https://www.ncbi.nlm.nih.gov/pubmed/27355614 http://dx.doi.org/10.7554/eLife.15567 |
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