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Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus

BACKGROUND: Previous studies have indicated that the VP19c protein and its homology play similar roles in capsid assembly of all Alphaherpesvirus subfamily. However, there is no report on the VP19c protein of duck enteritis virus (DEV). In this study, we expressed the DEV VP19c protein and presented...

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Autores principales: Xiang, Jun, Zhang, Shunchuan, Cheng, Anchun, Wang, Mingshu, Chang, Hua, Shen, Chanjuan, Zhu, Dekang, Jia, Renyong, Luo, Qihui, Chen, Zhengli, Chen, Xiaoyue
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050827/
https://www.ncbi.nlm.nih.gov/pubmed/21349183
http://dx.doi.org/10.1186/1743-422X-8-82
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author Xiang, Jun
Zhang, Shunchuan
Cheng, Anchun
Wang, Mingshu
Chang, Hua
Shen, Chanjuan
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Chen, Zhengli
Chen, Xiaoyue
author_facet Xiang, Jun
Zhang, Shunchuan
Cheng, Anchun
Wang, Mingshu
Chang, Hua
Shen, Chanjuan
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Chen, Zhengli
Chen, Xiaoyue
author_sort Xiang, Jun
collection PubMed
description BACKGROUND: Previous studies have indicated that the VP19c protein and its homology play similar roles in capsid assembly of all Alphaherpesvirus subfamily. However, there is no report on the VP19c protein of duck enteritis virus (DEV). In this study, we expressed the DEV VP19c protein and presented its antigenic properties. Moreover, we developed polyclonal antibody against the VP19c protein and characterized it. METHODS: A recombinant VP19c (rVP19c) and N-terminal were expressed in Escherichia coli (E.coli) and purified by Ni2+-affinity chromatography. The antigenic properties of the recombinant protein were determined by Western blot and indirect enzyme-linked immunosorbent assay (ELISA). Furthermore, the polyclonal antibodies against the purified recombinant proteins were produced and the titer of polyclonal antibody was determined by ELISA analysis. Finally, the antibody was used to recognize the VP19c in the cells infected with DEV in the immunofluorescence assay. RESULTS: The N-terminally His-tagged rVP19c and rVP19c(N) were produced as inclusion bodies in E. coli strain BL21 (DE3) with molecular weight of about 66 and 46 kDa. Then the proteins were purified to reach the level of homogeneity. Western blot and ELISA analysis that the rVP19c seems to be structurally and antigenically very similar to native VP19c and the N-terminus of VP19c may contain most antigenic linear-epitopes. Furthermore, ELISA analysis demonstrated that the titer of polyclonal antibody was approximately 1:12800, and in the immunofluorescence assay, the antibody was able to recognize the VP19c in the cells infected with DEV. CONCLUSIONS: To our knowledge, this was the first report on basic properties of DEV VP19c protein. In the present study, we obtained a high-level expression of the recombinant VP19c protein as well as high titers of rabbit polyclonal antibody against to VP19c protein. The anti-rVP19c serum was able to detect the VP19c protein in DEV infected cells and the VP19c protein targeted to the nucleus as distinct punctate speckles. This specific polyclonal antibody provides a good tool for further studying structural and functional characterization of DEV VP19c.
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spelling pubmed-30508272011-03-09 Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus Xiang, Jun Zhang, Shunchuan Cheng, Anchun Wang, Mingshu Chang, Hua Shen, Chanjuan Zhu, Dekang Jia, Renyong Luo, Qihui Chen, Zhengli Chen, Xiaoyue Virol J Research BACKGROUND: Previous studies have indicated that the VP19c protein and its homology play similar roles in capsid assembly of all Alphaherpesvirus subfamily. However, there is no report on the VP19c protein of duck enteritis virus (DEV). In this study, we expressed the DEV VP19c protein and presented its antigenic properties. Moreover, we developed polyclonal antibody against the VP19c protein and characterized it. METHODS: A recombinant VP19c (rVP19c) and N-terminal were expressed in Escherichia coli (E.coli) and purified by Ni2+-affinity chromatography. The antigenic properties of the recombinant protein were determined by Western blot and indirect enzyme-linked immunosorbent assay (ELISA). Furthermore, the polyclonal antibodies against the purified recombinant proteins were produced and the titer of polyclonal antibody was determined by ELISA analysis. Finally, the antibody was used to recognize the VP19c in the cells infected with DEV in the immunofluorescence assay. RESULTS: The N-terminally His-tagged rVP19c and rVP19c(N) were produced as inclusion bodies in E. coli strain BL21 (DE3) with molecular weight of about 66 and 46 kDa. Then the proteins were purified to reach the level of homogeneity. Western blot and ELISA analysis that the rVP19c seems to be structurally and antigenically very similar to native VP19c and the N-terminus of VP19c may contain most antigenic linear-epitopes. Furthermore, ELISA analysis demonstrated that the titer of polyclonal antibody was approximately 1:12800, and in the immunofluorescence assay, the antibody was able to recognize the VP19c in the cells infected with DEV. CONCLUSIONS: To our knowledge, this was the first report on basic properties of DEV VP19c protein. In the present study, we obtained a high-level expression of the recombinant VP19c protein as well as high titers of rabbit polyclonal antibody against to VP19c protein. The anti-rVP19c serum was able to detect the VP19c protein in DEV infected cells and the VP19c protein targeted to the nucleus as distinct punctate speckles. This specific polyclonal antibody provides a good tool for further studying structural and functional characterization of DEV VP19c. BioMed Central 2011-02-24 /pmc/articles/PMC3050827/ /pubmed/21349183 http://dx.doi.org/10.1186/1743-422X-8-82 Text en Copyright ©2011 Xiang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xiang, Jun
Zhang, Shunchuan
Cheng, Anchun
Wang, Mingshu
Chang, Hua
Shen, Chanjuan
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Chen, Zhengli
Chen, Xiaoyue
Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus
title Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus
title_full Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus
title_fullStr Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus
title_full_unstemmed Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus
title_short Expression and characterization of recombinant VP19c protein and N-terminal from duck enteritis virus
title_sort expression and characterization of recombinant vp19c protein and n-terminal from duck enteritis virus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050827/
https://www.ncbi.nlm.nih.gov/pubmed/21349183
http://dx.doi.org/10.1186/1743-422X-8-82
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