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Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening

Recombinant viruses labelled with fluorescent proteins are useful tools in molecular virology with multiple applications (e.g., studies on intracellular trafficking, protein localization, or gene activity). We generated by homologous recombination three recombinant cytomegaloviruses carrying the enh...

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Autores principales: Straschewski, Sarah, Warmer, Martin, Frascaroli, Giada, Hohenberg, Heinrich, Mertens, Thomas, Winkler, Michael
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820100/
https://www.ncbi.nlm.nih.gov/pubmed/20161802
http://dx.doi.org/10.1371/journal.pone.0009174
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author Straschewski, Sarah
Warmer, Martin
Frascaroli, Giada
Hohenberg, Heinrich
Mertens, Thomas
Winkler, Michael
author_facet Straschewski, Sarah
Warmer, Martin
Frascaroli, Giada
Hohenberg, Heinrich
Mertens, Thomas
Winkler, Michael
author_sort Straschewski, Sarah
collection PubMed
description Recombinant viruses labelled with fluorescent proteins are useful tools in molecular virology with multiple applications (e.g., studies on intracellular trafficking, protein localization, or gene activity). We generated by homologous recombination three recombinant cytomegaloviruses carrying the enhanced yellow fluorescent protein (EYFP) fused with the viral proteins IE-2, ppUL32 (pp150), and ppUL83 (pp65). In growth kinetics, the three viruses behaved all like wild type, even at low multiplicity of infection (MOI). The expression of all three fusion proteins was detected, and their respective localizations were the same as for the unmodified proteins in wild-type virus–infected cells. We established the in vivo measurement of fluorescence intensity and used the recombinant viruses to measure inhibition of viral replication by neutralizing antibodies or antiviral substances. The use of these viruses in a pilot screen based on fluorescence intensity and high-content analysis identified cellular kinase inhibitors that block viral replication. In summary, these viruses with individually EYFP-tagged proteins will be useful to study antiviral substances and the dynamics of viral infection in cell culture.
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spelling pubmed-28201002010-02-17 Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening Straschewski, Sarah Warmer, Martin Frascaroli, Giada Hohenberg, Heinrich Mertens, Thomas Winkler, Michael PLoS One Research Article Recombinant viruses labelled with fluorescent proteins are useful tools in molecular virology with multiple applications (e.g., studies on intracellular trafficking, protein localization, or gene activity). We generated by homologous recombination three recombinant cytomegaloviruses carrying the enhanced yellow fluorescent protein (EYFP) fused with the viral proteins IE-2, ppUL32 (pp150), and ppUL83 (pp65). In growth kinetics, the three viruses behaved all like wild type, even at low multiplicity of infection (MOI). The expression of all three fusion proteins was detected, and their respective localizations were the same as for the unmodified proteins in wild-type virus–infected cells. We established the in vivo measurement of fluorescence intensity and used the recombinant viruses to measure inhibition of viral replication by neutralizing antibodies or antiviral substances. The use of these viruses in a pilot screen based on fluorescence intensity and high-content analysis identified cellular kinase inhibitors that block viral replication. In summary, these viruses with individually EYFP-tagged proteins will be useful to study antiviral substances and the dynamics of viral infection in cell culture. Public Library of Science 2010-02-11 /pmc/articles/PMC2820100/ /pubmed/20161802 http://dx.doi.org/10.1371/journal.pone.0009174 Text en Straschewski et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Straschewski, Sarah
Warmer, Martin
Frascaroli, Giada
Hohenberg, Heinrich
Mertens, Thomas
Winkler, Michael
Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening
title Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening
title_full Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening
title_fullStr Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening
title_full_unstemmed Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening
title_short Human Cytomegaloviruses Expressing Yellow Fluorescent Fusion Proteins - Characterization and Use in Antiviral Screening
title_sort human cytomegaloviruses expressing yellow fluorescent fusion proteins - characterization and use in antiviral screening
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820100/
https://www.ncbi.nlm.nih.gov/pubmed/20161802
http://dx.doi.org/10.1371/journal.pone.0009174
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