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Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays

Poliomyelitis, caused by poliovirus, is on the verge of eradication, and the world is preparing to shift from live to inactivated polio vaccine. In view of the requirement of non-infectious reagents, especially protein antigens, for surveillance during the final phase of poliovirus eradication, we h...

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Detalles Bibliográficos
Autores principales: Uma, Madala, Rao, P.P., Nagalekshmi, K., Hegde, N.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040459/
https://www.ncbi.nlm.nih.gov/pubmed/27565898
http://dx.doi.org/10.1016/j.pep.2016.08.014
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author Uma, Madala
Rao, P.P.
Nagalekshmi, K.
Hegde, N.R.
author_facet Uma, Madala
Rao, P.P.
Nagalekshmi, K.
Hegde, N.R.
author_sort Uma, Madala
collection PubMed
description Poliomyelitis, caused by poliovirus, is on the verge of eradication, and the world is preparing to shift from live to inactivated polio vaccine. In view of the requirement of non-infectious reagents, especially protein antigens, for surveillance during the final phase of poliovirus eradication, we have attempted to generate reagents that may be of use for the development of diagnostic tests. Polioviral proteins VP0, VP3, VP1, and 3AB were expressed in Escherichia coli using the autoinduction system, purified, and the proteins were used to raise antisera in rabbits. All antisera detected all three serotypes of PV from infected cell lysates in enzyme-linked immunosorbent assay, immunofluorescence and western blotting.
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spelling pubmed-50404592016-12-01 Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays Uma, Madala Rao, P.P. Nagalekshmi, K. Hegde, N.R. Protein Expr Purif Article Poliomyelitis, caused by poliovirus, is on the verge of eradication, and the world is preparing to shift from live to inactivated polio vaccine. In view of the requirement of non-infectious reagents, especially protein antigens, for surveillance during the final phase of poliovirus eradication, we have attempted to generate reagents that may be of use for the development of diagnostic tests. Polioviral proteins VP0, VP3, VP1, and 3AB were expressed in Escherichia coli using the autoinduction system, purified, and the proteins were used to raise antisera in rabbits. All antisera detected all three serotypes of PV from infected cell lysates in enzyme-linked immunosorbent assay, immunofluorescence and western blotting. Academic Press 2016-12 /pmc/articles/PMC5040459/ /pubmed/27565898 http://dx.doi.org/10.1016/j.pep.2016.08.014 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Uma, Madala
Rao, P.P.
Nagalekshmi, K.
Hegde, N.R.
Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays
title Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays
title_full Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays
title_fullStr Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays
title_full_unstemmed Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays
title_short Expression and purification of polioviral proteins in E. coli, and production of antisera as reagents for immunological assays
title_sort expression and purification of polioviral proteins in e. coli, and production of antisera as reagents for immunological assays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040459/
https://www.ncbi.nlm.nih.gov/pubmed/27565898
http://dx.doi.org/10.1016/j.pep.2016.08.014
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