Cargando…
Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps
A key obstacle in uncovering the orchestration between molecular and cellular events is the vastly different length scales on which they occur. We describe here a methodology for ultrastructurally mapping regions of cells and tissue as large as 1 mm(2) at nanometer resolution. Our approach employs s...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413355/ https://www.ncbi.nlm.nih.gov/pubmed/22869601 http://dx.doi.org/10.1083/jcb.201201140 |
_version_ | 1782240048290201600 |
---|---|
author | Faas, Frank G.A. Avramut, M. Cristina M. van den Berg, Bernard Mommaas, A. Mieke Koster, Abraham J. Ravelli, Raimond B.G. |
author_facet | Faas, Frank G.A. Avramut, M. Cristina M. van den Berg, Bernard Mommaas, A. Mieke Koster, Abraham J. Ravelli, Raimond B.G. |
author_sort | Faas, Frank G.A. |
collection | PubMed |
description | A key obstacle in uncovering the orchestration between molecular and cellular events is the vastly different length scales on which they occur. We describe here a methodology for ultrastructurally mapping regions of cells and tissue as large as 1 mm(2) at nanometer resolution. Our approach employs standard transmission electron microscopy, rapid automated data collection, and stitching to create large virtual slides. It greatly facilitates correlative light-electron microscopy studies to relate structure and function and provides a genuine representation of ultrastructural events. The method is scalable as illustrated by slides up to 281 gigapixels in size. Here, we applied virtual nanoscopy in a correlative light-electron microscopy study to address the role of the endothelial glycocalyx in protein leakage over the glomerular filtration barrier, in an immunogold labeling study of internalization of oncolytic reovirus in human dendritic cells, in a cryo-electron microscopy study of intact vitrified mouse embryonic cells, and in an ultrastructural mapping of a complete zebrafish embryo slice. |
format | Online Article Text |
id | pubmed-3413355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34133552013-02-06 Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps Faas, Frank G.A. Avramut, M. Cristina M. van den Berg, Bernard Mommaas, A. Mieke Koster, Abraham J. Ravelli, Raimond B.G. J Cell Biol Research Articles A key obstacle in uncovering the orchestration between molecular and cellular events is the vastly different length scales on which they occur. We describe here a methodology for ultrastructurally mapping regions of cells and tissue as large as 1 mm(2) at nanometer resolution. Our approach employs standard transmission electron microscopy, rapid automated data collection, and stitching to create large virtual slides. It greatly facilitates correlative light-electron microscopy studies to relate structure and function and provides a genuine representation of ultrastructural events. The method is scalable as illustrated by slides up to 281 gigapixels in size. Here, we applied virtual nanoscopy in a correlative light-electron microscopy study to address the role of the endothelial glycocalyx in protein leakage over the glomerular filtration barrier, in an immunogold labeling study of internalization of oncolytic reovirus in human dendritic cells, in a cryo-electron microscopy study of intact vitrified mouse embryonic cells, and in an ultrastructural mapping of a complete zebrafish embryo slice. The Rockefeller University Press 2012-08-06 /pmc/articles/PMC3413355/ /pubmed/22869601 http://dx.doi.org/10.1083/jcb.201201140 Text en © 2012 Faas et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Faas, Frank G.A. Avramut, M. Cristina M. van den Berg, Bernard Mommaas, A. Mieke Koster, Abraham J. Ravelli, Raimond B.G. Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps |
title | Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps |
title_full | Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps |
title_fullStr | Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps |
title_full_unstemmed | Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps |
title_short | Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps |
title_sort | virtual nanoscopy: generation of ultra-large high resolution electron microscopy maps |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413355/ https://www.ncbi.nlm.nih.gov/pubmed/22869601 http://dx.doi.org/10.1083/jcb.201201140 |
work_keys_str_mv | AT faasfrankga virtualnanoscopygenerationofultralargehighresolutionelectronmicroscopymaps AT avramutmcristina virtualnanoscopygenerationofultralargehighresolutionelectronmicroscopymaps AT mvandenbergbernard virtualnanoscopygenerationofultralargehighresolutionelectronmicroscopymaps AT mommaasamieke virtualnanoscopygenerationofultralargehighresolutionelectronmicroscopymaps AT kosterabrahamj virtualnanoscopygenerationofultralargehighresolutionelectronmicroscopymaps AT ravelliraimondbg virtualnanoscopygenerationofultralargehighresolutionelectronmicroscopymaps |