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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...
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/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. |
format | Online Article Text |
id | pubmed-4094034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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