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Fluorescence cryo-microscopy: current challenges and prospects

Studying biological structures with fine details does not only require a microscope with high resolution, but also a sample preparation process that preserves the structures in a near-native state. Live-cell imaging is restricted mostly to the field of light microscopy. For studies requiring much hi...

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Detalles Bibliográficos
Autores principales: Kaufmann, Rainer, Hagen, Christoph, Grünewald, Kay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094034/
https://www.ncbi.nlm.nih.gov/pubmed/24951858
http://dx.doi.org/10.1016/j.cbpa.2014.05.007
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author Kaufmann, Rainer
Hagen, Christoph
Grünewald, Kay
author_facet Kaufmann, Rainer
Hagen, Christoph
Grünewald, Kay
author_sort Kaufmann, Rainer
collection PubMed
description Studying biological structures with fine details does not only require a microscope with high resolution, but also a sample preparation process that preserves the structures in a near-native state. Live-cell imaging is restricted mostly to the field of light microscopy. For studies requiring much higher resolution, fast freezing techniques (vitrification) are successfully used to immobilize the sample in a near-native state for imaging with electron and X-ray cryo-microscopy. Fluorescence cryo-microscopy combines imaging of vitrified samples with the advantages of fluorescence labeling of biological structures. Technical considerations as well as the behavior of fluorophores at low temperatures have to be taken into account for developing or adapting super-resolution methods under cryo conditions to exploit the full potential of this technique.
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spelling pubmed-40940342014-07-23 Fluorescence cryo-microscopy: current challenges and prospects Kaufmann, Rainer Hagen, Christoph Grünewald, Kay Curr Opin Chem Biol Article Studying biological structures with fine details does not only require a microscope with high resolution, but also a sample preparation process that preserves the structures in a near-native state. Live-cell imaging is restricted mostly to the field of light microscopy. For studies requiring much higher resolution, fast freezing techniques (vitrification) are successfully used to immobilize the sample in a near-native state for imaging with electron and X-ray cryo-microscopy. Fluorescence cryo-microscopy combines imaging of vitrified samples with the advantages of fluorescence labeling of biological structures. Technical considerations as well as the behavior of fluorophores at low temperatures have to be taken into account for developing or adapting super-resolution methods under cryo conditions to exploit the full potential of this technique. Elsevier 2014-06 /pmc/articles/PMC4094034/ /pubmed/24951858 http://dx.doi.org/10.1016/j.cbpa.2014.05.007 Text en © 2014 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
Kaufmann, Rainer
Hagen, Christoph
Grünewald, Kay
Fluorescence cryo-microscopy: current challenges and prospects
title Fluorescence cryo-microscopy: current challenges and prospects
title_full Fluorescence cryo-microscopy: current challenges and prospects
title_fullStr Fluorescence cryo-microscopy: current challenges and prospects
title_full_unstemmed Fluorescence cryo-microscopy: current challenges and prospects
title_short Fluorescence cryo-microscopy: current challenges and prospects
title_sort fluorescence cryo-microscopy: current challenges and prospects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094034/
https://www.ncbi.nlm.nih.gov/pubmed/24951858
http://dx.doi.org/10.1016/j.cbpa.2014.05.007
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