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High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers()
Correlative light and electron microscopy (CLEM) is an emerging technique which combines functional information provided by fluorescence microscopy (FM) with the high-resolution structural information of electron microscopy (EM). So far, correlative cryo microscopy of frozen-hydrated samples has not...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045203/ https://www.ncbi.nlm.nih.gov/pubmed/24262358 http://dx.doi.org/10.1016/j.ultramic.2013.10.011 |
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author | Schellenberger, Pascale Kaufmann, Rainer Siebert, C. Alistair Hagen, Christoph Wodrich, Harald Grünewald, Kay |
author_facet | Schellenberger, Pascale Kaufmann, Rainer Siebert, C. Alistair Hagen, Christoph Wodrich, Harald Grünewald, Kay |
author_sort | Schellenberger, Pascale |
collection | PubMed |
description | Correlative light and electron microscopy (CLEM) is an emerging technique which combines functional information provided by fluorescence microscopy (FM) with the high-resolution structural information of electron microscopy (EM). So far, correlative cryo microscopy of frozen-hydrated samples has not reached better than micrometre range accuracy. Here, a method is presented that enables the correlation between fluorescently tagged proteins and electron cryo tomography (cryoET) data with nanometre range precision. Specifically, thin areas of vitrified whole cells are examined by correlative fluorescence cryo microscopy (cryoFM) and cryoET. Novel aspects of the presented cryoCLEM workflow not only include the implementation of two independent electron dense fluorescent markers to improve the precision of the alignment, but also the ability of obtaining an estimate of the correlation accuracy for each individual object of interest. The correlative workflow from plunge-freezing to cryoET is detailed step-by-step for the example of locating fluorescence-labelled adenovirus particles trafficking inside a cell. |
format | Online Article Text |
id | pubmed-4045203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-40452032014-08-01 High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() Schellenberger, Pascale Kaufmann, Rainer Siebert, C. Alistair Hagen, Christoph Wodrich, Harald Grünewald, Kay Ultramicroscopy Article Correlative light and electron microscopy (CLEM) is an emerging technique which combines functional information provided by fluorescence microscopy (FM) with the high-resolution structural information of electron microscopy (EM). So far, correlative cryo microscopy of frozen-hydrated samples has not reached better than micrometre range accuracy. Here, a method is presented that enables the correlation between fluorescently tagged proteins and electron cryo tomography (cryoET) data with nanometre range precision. Specifically, thin areas of vitrified whole cells are examined by correlative fluorescence cryo microscopy (cryoFM) and cryoET. Novel aspects of the presented cryoCLEM workflow not only include the implementation of two independent electron dense fluorescent markers to improve the precision of the alignment, but also the ability of obtaining an estimate of the correlation accuracy for each individual object of interest. The correlative workflow from plunge-freezing to cryoET is detailed step-by-step for the example of locating fluorescence-labelled adenovirus particles trafficking inside a cell. Elsevier 2014-08 /pmc/articles/PMC4045203/ /pubmed/24262358 http://dx.doi.org/10.1016/j.ultramic.2013.10.011 Text en © 2013 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Schellenberger, Pascale Kaufmann, Rainer Siebert, C. Alistair Hagen, Christoph Wodrich, Harald Grünewald, Kay High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
title | High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
title_full | High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
title_fullStr | High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
title_full_unstemmed | High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
title_short | High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
title_sort | high-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045203/ https://www.ncbi.nlm.nih.gov/pubmed/24262358 http://dx.doi.org/10.1016/j.ultramic.2013.10.011 |
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