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[33] Using confocal microscopy to study virus binding and entry into cells
The chapter presents a discussion on the study of virus binding and entry into cells by using confocal microscopy. For the study new approaches to study vaccinia virus (VV), binding and entry based on confocal microscopy are developed. These techniques do not require virus purification or labeling a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
1999
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172951/ https://www.ncbi.nlm.nih.gov/pubmed/10506996 http://dx.doi.org/10.1016/S0076-6879(99)07035-4 |
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author | Vanderplasschen, Alain Smith, Geoffrey L. |
author_facet | Vanderplasschen, Alain Smith, Geoffrey L. |
author_sort | Vanderplasschen, Alain |
collection | PubMed |
description | The chapter presents a discussion on the study of virus binding and entry into cells by using confocal microscopy. For the study new approaches to study vaccinia virus (VV), binding and entry based on confocal microscopy are developed. These techniques do not require virus purification or labeling and generate data that reveal the absolute numbers of virus particles that have bound to or have entered into individual cells. The chapter describes these techniques and then illustrates with some of the results obtained. These methods should be applicable to any virus larger than 50 nm. The chapter discusses the way these techniques have generated data that cannot be obtained with classical binding or entry assays. Vaccina virus is the prototype of the poxvirus family. These are DNA viruses that replicate in the cell cytoplasm and have genomes between 150 and 300 kbp. These techniques are presented with a study of the binding and entry of VV. The methods have been particularly useful for studying VV because this virus produces two different forms of infectious virion that are antigenically and biologically distinct and are produced in widely differing amounts. Moreover, the extracellular enveloped virus (EEV) form of VV cannot be purified from contaminating IMV without disrupting the integrity of the outer envelope. |
format | Online Article Text |
id | pubmed-7172951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71729512020-04-22 [33] Using confocal microscopy to study virus binding and entry into cells Vanderplasschen, Alain Smith, Geoffrey L. Methods Enzymol Article The chapter presents a discussion on the study of virus binding and entry into cells by using confocal microscopy. For the study new approaches to study vaccinia virus (VV), binding and entry based on confocal microscopy are developed. These techniques do not require virus purification or labeling and generate data that reveal the absolute numbers of virus particles that have bound to or have entered into individual cells. The chapter describes these techniques and then illustrates with some of the results obtained. These methods should be applicable to any virus larger than 50 nm. The chapter discusses the way these techniques have generated data that cannot be obtained with classical binding or entry assays. Vaccina virus is the prototype of the poxvirus family. These are DNA viruses that replicate in the cell cytoplasm and have genomes between 150 and 300 kbp. These techniques are presented with a study of the binding and entry of VV. The methods have been particularly useful for studying VV because this virus produces two different forms of infectious virion that are antigenically and biologically distinct and are produced in widely differing amounts. Moreover, the extracellular enveloped virus (EEV) form of VV cannot be purified from contaminating IMV without disrupting the integrity of the outer envelope. Published by Elsevier Inc. 1999 2004-01-07 /pmc/articles/PMC7172951/ /pubmed/10506996 http://dx.doi.org/10.1016/S0076-6879(99)07035-4 Text en Copyright © 1999 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Vanderplasschen, Alain Smith, Geoffrey L. [33] Using confocal microscopy to study virus binding and entry into cells |
title | [33] Using confocal microscopy to study virus binding and entry into cells |
title_full | [33] Using confocal microscopy to study virus binding and entry into cells |
title_fullStr | [33] Using confocal microscopy to study virus binding and entry into cells |
title_full_unstemmed | [33] Using confocal microscopy to study virus binding and entry into cells |
title_short | [33] Using confocal microscopy to study virus binding and entry into cells |
title_sort | [33] using confocal microscopy to study virus binding and entry into cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172951/ https://www.ncbi.nlm.nih.gov/pubmed/10506996 http://dx.doi.org/10.1016/S0076-6879(99)07035-4 |
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