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Fluorescence Molecular Painting of Enveloped Viruses

In this study, we describe a versatile, flexible, and quick method to label different families of enveloped viruses with glycosylphosphatidylinositol-modified green fluorescent protein, termed fluorescence molecular painting (FMP). As an example for a potential application, we investigated virus att...

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Detalles Bibliográficos
Autores principales: Metzner, Christoph, Kochan, Feliks, Dangerfield, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Humana Press Inc 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524503/
https://www.ncbi.nlm.nih.gov/pubmed/23104232
http://dx.doi.org/10.1007/s12033-012-9616-6
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author Metzner, Christoph
Kochan, Feliks
Dangerfield, John A.
author_facet Metzner, Christoph
Kochan, Feliks
Dangerfield, John A.
author_sort Metzner, Christoph
collection PubMed
description In this study, we describe a versatile, flexible, and quick method to label different families of enveloped viruses with glycosylphosphatidylinositol-modified green fluorescent protein, termed fluorescence molecular painting (FMP). As an example for a potential application, we investigated virus attachment by means of flow cytometry to determine if viral binding behavior may be analyzed after FMP of enveloped viruses. Virus attachment was inhibited by using either dextran sulfate or by blocking attachment sites with virus pre-treatment. Results from the FMP–flow cytometry approach were verified by immunoblotting and enzyme-linked immunosorbent assay. Since the modification strategy is applicable to a broad range of proteins and viruses, variations of this method may be useful in a range of research and applied applications from bio-distribution studies to vaccine development and targeted infection for gene delivery.
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spelling pubmed-35245032012-12-21 Fluorescence Molecular Painting of Enveloped Viruses Metzner, Christoph Kochan, Feliks Dangerfield, John A. Mol Biotechnol Research In this study, we describe a versatile, flexible, and quick method to label different families of enveloped viruses with glycosylphosphatidylinositol-modified green fluorescent protein, termed fluorescence molecular painting (FMP). As an example for a potential application, we investigated virus attachment by means of flow cytometry to determine if viral binding behavior may be analyzed after FMP of enveloped viruses. Virus attachment was inhibited by using either dextran sulfate or by blocking attachment sites with virus pre-treatment. Results from the FMP–flow cytometry approach were verified by immunoblotting and enzyme-linked immunosorbent assay. Since the modification strategy is applicable to a broad range of proteins and viruses, variations of this method may be useful in a range of research and applied applications from bio-distribution studies to vaccine development and targeted infection for gene delivery. Humana Press Inc 2012-10-28 2013 /pmc/articles/PMC3524503/ /pubmed/23104232 http://dx.doi.org/10.1007/s12033-012-9616-6 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research
Metzner, Christoph
Kochan, Feliks
Dangerfield, John A.
Fluorescence Molecular Painting of Enveloped Viruses
title Fluorescence Molecular Painting of Enveloped Viruses
title_full Fluorescence Molecular Painting of Enveloped Viruses
title_fullStr Fluorescence Molecular Painting of Enveloped Viruses
title_full_unstemmed Fluorescence Molecular Painting of Enveloped Viruses
title_short Fluorescence Molecular Painting of Enveloped Viruses
title_sort fluorescence molecular painting of enveloped viruses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524503/
https://www.ncbi.nlm.nih.gov/pubmed/23104232
http://dx.doi.org/10.1007/s12033-012-9616-6
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