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Super induction of dengue virus NS1 protein in E. coli
The non-structural protein 1 (NS1) of dengue virus is a useful target for diagnostics of dengue infection since the protein is abundantly circulating in blood during the acute phase of the disease. Prior work has established that secreted NS1 levels in plasma correlates with viremia levels and hence...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129434/ https://www.ncbi.nlm.nih.gov/pubmed/19232392 http://dx.doi.org/10.1016/j.pep.2009.02.003 |
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author | Das, Dipankar Mongkolaungkoon, Sunundha Suresh, Mavanur R. |
author_facet | Das, Dipankar Mongkolaungkoon, Sunundha Suresh, Mavanur R. |
author_sort | Das, Dipankar |
collection | PubMed |
description | The non-structural protein 1 (NS1) of dengue virus is a useful target for diagnostics of dengue infection since the protein is abundantly circulating in blood during the acute phase of the disease. Prior work has established that secreted NS1 levels in plasma correlates with viremia levels and hence can also be used to diagnose patients at the risk for developing dengue hemorrhagic fever. Thus detection of non-structural dengue antigens may be of benefit for an early rapid diagnosis of dengue infection due to its long half life in the blood. Here we describe a simple and efficient method for the expression of NS1 in Escherichia coli, which could potentially be used to develop monoclonal and bispecific antibodies for point of care diagnostics. E. coli codon optimized synthetic full-length NS1 gene of dengue serotype 1 (DEN-1) was successfully cloned and expressed in very high-level as inclusion bodies. The NS1 protein was successfully affinity purified and refolded as a recombinant NS1 (rNS1) protein in E. coli and yield was 230–250 mg/L of bacterial culture. The rNS1 protein was used to immunize mice for hybridoma development. The polyclonal antiserum from animals immunized with this rNS1 protein was found to specifically recognize the rNS1, thus demonstrating the immunogenic nature of the protein. The rNS1 protein purified from E. coli could be useful for developing a sensitive serum diagnostic assay to monitor dengue outbreaks. |
format | Online Article Text |
id | pubmed-7129434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71294342020-04-08 Super induction of dengue virus NS1 protein in E. coli Das, Dipankar Mongkolaungkoon, Sunundha Suresh, Mavanur R. Protein Expr Purif Article The non-structural protein 1 (NS1) of dengue virus is a useful target for diagnostics of dengue infection since the protein is abundantly circulating in blood during the acute phase of the disease. Prior work has established that secreted NS1 levels in plasma correlates with viremia levels and hence can also be used to diagnose patients at the risk for developing dengue hemorrhagic fever. Thus detection of non-structural dengue antigens may be of benefit for an early rapid diagnosis of dengue infection due to its long half life in the blood. Here we describe a simple and efficient method for the expression of NS1 in Escherichia coli, which could potentially be used to develop monoclonal and bispecific antibodies for point of care diagnostics. E. coli codon optimized synthetic full-length NS1 gene of dengue serotype 1 (DEN-1) was successfully cloned and expressed in very high-level as inclusion bodies. The NS1 protein was successfully affinity purified and refolded as a recombinant NS1 (rNS1) protein in E. coli and yield was 230–250 mg/L of bacterial culture. The rNS1 protein was used to immunize mice for hybridoma development. The polyclonal antiserum from animals immunized with this rNS1 protein was found to specifically recognize the rNS1, thus demonstrating the immunogenic nature of the protein. The rNS1 protein purified from E. coli could be useful for developing a sensitive serum diagnostic assay to monitor dengue outbreaks. Elsevier Inc. 2009-07 2009-02-14 /pmc/articles/PMC7129434/ /pubmed/19232392 http://dx.doi.org/10.1016/j.pep.2009.02.003 Text en Copyright © 2009 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Das, Dipankar Mongkolaungkoon, Sunundha Suresh, Mavanur R. Super induction of dengue virus NS1 protein in E. coli |
title | Super induction of dengue virus NS1 protein in E. coli |
title_full | Super induction of dengue virus NS1 protein in E. coli |
title_fullStr | Super induction of dengue virus NS1 protein in E. coli |
title_full_unstemmed | Super induction of dengue virus NS1 protein in E. coli |
title_short | Super induction of dengue virus NS1 protein in E. coli |
title_sort | super induction of dengue virus ns1 protein in e. coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129434/ https://www.ncbi.nlm.nih.gov/pubmed/19232392 http://dx.doi.org/10.1016/j.pep.2009.02.003 |
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