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PMID: 15114023 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Viral glycoprotein-mediated cell fusion assays using vaccinia virus vectors.

Methods in molecular biology (Clifton, N.J.) ·Vol. 269 ·2004-00-00 ·Pages 309-32

Bossart KN, Broder CC

Abstract

The vaccinia virus-based expression of viral envelope glycoprotein genes-derived from enveloped viruses that infect their respective host cells through a pH-independent mechanism of membrane fusion-has been a powerful tool in helping to characterize these important attachment and fusion proteins. The cellular expression of these viral envelope glycoproteins has allowed for the measurement of membrane fusion events using cell-cell fusion or syncytia formation. This method has been enhanced by the addition of a reporter-gene system to the vaccinia virus-based cell-cell fusion assay. This improvement has provided a high-throughput and quantitative aspect to this assay, which can serve as a surrogate for virus entry and is therefore ideally suited in the characterization of numerous enveloped viruses, including biological safety level-4 (BSL-4) agents. This chapter will detail the methods of the vaccinia virus-based reporter-gene fusion assay and how it may be used to characterize the fusion mediated by the BSL-4-classified Hendra and Nipah viruses.

MeSH Terms
Cell Fusion/methods Cell Line Genetic Vectors Membrane Glycoproteins/biosynthesis,metabolism,physiology Vaccinia virus/genetics,physiology Viral Envelope Proteins/physiology Viral Fusion Proteins/physiology
Chemicals
Membrane Glycoproteins Viral Envelope Proteins Viral Fusion Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bossart Katharine N
Department of Microbiology & Molecular Genetics, Medical College of Wisconsin, Milwaukee, WI, USA.
Broder Christopher C
Article Info
Journal
Methods in molecular biology (Clifton, N.J.)
Abbr.
Methods Mol Biol
ISSN
1064-3745
Published
2004-00-00
Pages
309-32
Language
English
Region
United States
NLM ID
9214969
Subset
IM
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