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Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus

Infectious bronchitis virus (IBV), a group 3 coronavirus, produces three proteins (IBV E, IBV 3a, and IBV 3b) from subgenomic mRNA 3 during infection. IBV E, a viral envelope protein, plays a role in virus budding, possibly by altering membrane morphology at the virus assembly site. In addition to t...

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Detalles Bibliográficos
Autores principales: Pendleton, Amanda R., Machamer, Carolyn E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120050/
https://www.ncbi.nlm.nih.gov/pubmed/19057877
http://dx.doi.org/10.1007/978-1-59745-181-9_14
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author Pendleton, Amanda R.
Machamer, Carolyn E.
author_facet Pendleton, Amanda R.
Machamer, Carolyn E.
author_sort Pendleton, Amanda R.
collection PubMed
description Infectious bronchitis virus (IBV), a group 3 coronavirus, produces three proteins (IBV E, IBV 3a, and IBV 3b) from subgenomic mRNA 3 during infection. IBV E, a viral envelope protein, plays a role in virus budding, possibly by altering membrane morphology at the virus assembly site. In addition to this role, IBV E may also function as a viroporin, although no data from infected cells have confirmed this possibility definitively. Conversely, the IBV 3a and IBV 3b proteins are nonstructural proteins. These proteins are dispensable for replication in cell culture, but are thought to be important for infection of the natural host. This chapter details methods for generating and screening antibodies to these gene 3 proteins. Antibodies were raised in rabbits following inoculation with IBV-specific peptides and GST fusion proteins, and were screened by immunofluorescence, radioimmunoprecipitation, and immunoblotting.
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spelling pubmed-71200502020-04-06 Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus Pendleton, Amanda R. Machamer, Carolyn E. SARS- and Other Coronaviruses Article Infectious bronchitis virus (IBV), a group 3 coronavirus, produces three proteins (IBV E, IBV 3a, and IBV 3b) from subgenomic mRNA 3 during infection. IBV E, a viral envelope protein, plays a role in virus budding, possibly by altering membrane morphology at the virus assembly site. In addition to this role, IBV E may also function as a viroporin, although no data from infected cells have confirmed this possibility definitively. Conversely, the IBV 3a and IBV 3b proteins are nonstructural proteins. These proteins are dispensable for replication in cell culture, but are thought to be important for infection of the natural host. This chapter details methods for generating and screening antibodies to these gene 3 proteins. Antibodies were raised in rabbits following inoculation with IBV-specific peptides and GST fusion proteins, and were screened by immunofluorescence, radioimmunoprecipitation, and immunoblotting. 2007-11-28 /pmc/articles/PMC7120050/ /pubmed/19057877 http://dx.doi.org/10.1007/978-1-59745-181-9_14 Text en © Humana Press, a part of Springer Science+Business Media, LLC 2008 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Pendleton, Amanda R.
Machamer, Carolyn E.
Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus
title Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus
title_full Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus
title_fullStr Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus
title_full_unstemmed Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus
title_short Generating Antibodies to the Gene 3 Proteins of Infectious Bronchitis Virus
title_sort generating antibodies to the gene 3 proteins of infectious bronchitis virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120050/
https://www.ncbi.nlm.nih.gov/pubmed/19057877
http://dx.doi.org/10.1007/978-1-59745-181-9_14
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