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Photonic-chip assisted correlative light and electron microscopy
Correlative light and electron microscopy (CLEM) unifies the versatility of light microscopy (LM) with the high resolution of electron microscopy (EM), allowing one to zoom into the complex organization of cells. Here, we introduce photonic chip assisted CLEM, enabling multi-modal total internal ref...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721707/ https://www.ncbi.nlm.nih.gov/pubmed/33288833 http://dx.doi.org/10.1038/s42003-020-01473-4 |
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author | Tinguely, Jean-Claude Steyer, Anna Maria Øie, Cristina Ionica Helle, Øystein Ivar Dullo, Firehun Tsige Olsen, Randi McCourt, Peter Schwab, Yannick Ahluwalia, Balpreet Singh |
author_facet | Tinguely, Jean-Claude Steyer, Anna Maria Øie, Cristina Ionica Helle, Øystein Ivar Dullo, Firehun Tsige Olsen, Randi McCourt, Peter Schwab, Yannick Ahluwalia, Balpreet Singh |
author_sort | Tinguely, Jean-Claude |
collection | PubMed |
description | Correlative light and electron microscopy (CLEM) unifies the versatility of light microscopy (LM) with the high resolution of electron microscopy (EM), allowing one to zoom into the complex organization of cells. Here, we introduce photonic chip assisted CLEM, enabling multi-modal total internal reflection fluorescence (TIRF) microscopy over large field of view and high precision localization of the target area of interest within EM. The photonic chips are used as a substrate to hold, to illuminate and to provide landmarking of the sample through specially designed grid-like numbering systems. Using this approach, we demonstrate its applicability for tracking the area of interest, imaging the three-dimensional (3D) structural organization of nano-sized morphological features on liver sinusoidal endothelial cells such as fenestrations (trans-cytoplasmic nanopores), and correlating specific endo-lysosomal compartments with its cargo protein upon endocytosis. |
format | Online Article Text |
id | pubmed-7721707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77217072020-12-11 Photonic-chip assisted correlative light and electron microscopy Tinguely, Jean-Claude Steyer, Anna Maria Øie, Cristina Ionica Helle, Øystein Ivar Dullo, Firehun Tsige Olsen, Randi McCourt, Peter Schwab, Yannick Ahluwalia, Balpreet Singh Commun Biol Article Correlative light and electron microscopy (CLEM) unifies the versatility of light microscopy (LM) with the high resolution of electron microscopy (EM), allowing one to zoom into the complex organization of cells. Here, we introduce photonic chip assisted CLEM, enabling multi-modal total internal reflection fluorescence (TIRF) microscopy over large field of view and high precision localization of the target area of interest within EM. The photonic chips are used as a substrate to hold, to illuminate and to provide landmarking of the sample through specially designed grid-like numbering systems. Using this approach, we demonstrate its applicability for tracking the area of interest, imaging the three-dimensional (3D) structural organization of nano-sized morphological features on liver sinusoidal endothelial cells such as fenestrations (trans-cytoplasmic nanopores), and correlating specific endo-lysosomal compartments with its cargo protein upon endocytosis. Nature Publishing Group UK 2020-12-07 /pmc/articles/PMC7721707/ /pubmed/33288833 http://dx.doi.org/10.1038/s42003-020-01473-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tinguely, Jean-Claude Steyer, Anna Maria Øie, Cristina Ionica Helle, Øystein Ivar Dullo, Firehun Tsige Olsen, Randi McCourt, Peter Schwab, Yannick Ahluwalia, Balpreet Singh Photonic-chip assisted correlative light and electron microscopy |
title | Photonic-chip assisted correlative light and electron microscopy |
title_full | Photonic-chip assisted correlative light and electron microscopy |
title_fullStr | Photonic-chip assisted correlative light and electron microscopy |
title_full_unstemmed | Photonic-chip assisted correlative light and electron microscopy |
title_short | Photonic-chip assisted correlative light and electron microscopy |
title_sort | photonic-chip assisted correlative light and electron microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721707/ https://www.ncbi.nlm.nih.gov/pubmed/33288833 http://dx.doi.org/10.1038/s42003-020-01473-4 |
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