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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...

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Autores principales: Schellenberger, Pascale, Kaufmann, Rainer, Siebert, C. Alistair, Hagen, Christoph, Wodrich, Harald, Grünewald, Kay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
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.
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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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