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Dynamic force microscopy for imaging of viruses under physiological conditions

Dynamic force microscopy (DFM) allows imaging of the structure and the assessment of the function of biological specimens in their physiological environment. In DFM, the cantilever is oscillated at a given frequency and touches the sample only at the end of its downward movement. Accordingly, the pr...

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Autores principales: Kienberger, Ferry, Zhu, Rong, Moser, Rosita, Rankl, Christian, Blaas, Dieter, Hinterdorfer, Peter
Formato: Texto
Lenguaje:English
Publicado: Biological Procedures Online 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC443560/
https://www.ncbi.nlm.nih.gov/pubmed/15243650
http://dx.doi.org/10.1251/bpo80
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author Kienberger, Ferry
Zhu, Rong
Moser, Rosita
Rankl, Christian
Blaas, Dieter
Hinterdorfer, Peter
author_facet Kienberger, Ferry
Zhu, Rong
Moser, Rosita
Rankl, Christian
Blaas, Dieter
Hinterdorfer, Peter
author_sort Kienberger, Ferry
collection PubMed
description Dynamic force microscopy (DFM) allows imaging of the structure and the assessment of the function of biological specimens in their physiological environment. In DFM, the cantilever is oscillated at a given frequency and touches the sample only at the end of its downward movement. Accordingly, the problem of lateral forces displacing or even destroying bio-molecules is virtually inexistent as the contact time and friction forces are reduced. Here, we describe the use of DFM in studies of human rhinovirus serotype 2 (HRV2) weakly adhering to mica surfaces. The capsid of HRV2 was reproducibly imaged without any displacement of the virus. Release of the genomic RNA from the virions was initiated by exposure to low pH buffer and snapshots of the extrusion process were obtained. In the following, the technical details of previous DFM investigations of HRV2 are summarized.
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spelling pubmed-4435602004-07-07 Dynamic force microscopy for imaging of viruses under physiological conditions Kienberger, Ferry Zhu, Rong Moser, Rosita Rankl, Christian Blaas, Dieter Hinterdorfer, Peter Biol Proced Online Research Article Dynamic force microscopy (DFM) allows imaging of the structure and the assessment of the function of biological specimens in their physiological environment. In DFM, the cantilever is oscillated at a given frequency and touches the sample only at the end of its downward movement. Accordingly, the problem of lateral forces displacing or even destroying bio-molecules is virtually inexistent as the contact time and friction forces are reduced. Here, we describe the use of DFM in studies of human rhinovirus serotype 2 (HRV2) weakly adhering to mica surfaces. The capsid of HRV2 was reproducibly imaged without any displacement of the virus. Release of the genomic RNA from the virions was initiated by exposure to low pH buffer and snapshots of the extrusion process were obtained. In the following, the technical details of previous DFM investigations of HRV2 are summarized. Biological Procedures Online 2004-06-29 /pmc/articles/PMC443560/ /pubmed/15243650 http://dx.doi.org/10.1251/bpo80 Text en Copyright © June 06, 2004, F Kienberger et al. Published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted.
spellingShingle Research Article
Kienberger, Ferry
Zhu, Rong
Moser, Rosita
Rankl, Christian
Blaas, Dieter
Hinterdorfer, Peter
Dynamic force microscopy for imaging of viruses under physiological conditions
title Dynamic force microscopy for imaging of viruses under physiological conditions
title_full Dynamic force microscopy for imaging of viruses under physiological conditions
title_fullStr Dynamic force microscopy for imaging of viruses under physiological conditions
title_full_unstemmed Dynamic force microscopy for imaging of viruses under physiological conditions
title_short Dynamic force microscopy for imaging of viruses under physiological conditions
title_sort dynamic force microscopy for imaging of viruses under physiological conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC443560/
https://www.ncbi.nlm.nih.gov/pubmed/15243650
http://dx.doi.org/10.1251/bpo80
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