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New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants

The novel viral vectors PVX-CP AltMV and PVXdt-CP AltMV are superexpressors of the capsid protein (CP). These viral vectors were constructed on the basis of the potato virus X (PVX) genome andAlternantheramosaic virus (AltMV) CP gene. The expression, based on the hybrid viral vectors, is genetically...

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Autores principales: Tyulkina, L.G., Skurat, E.V., Frolova, O.Yu., Komarova, T.V., Karger, E.M., Atabekov, I.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A.I. Gordeyev 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347618/
https://www.ncbi.nlm.nih.gov/pubmed/22649706
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author Tyulkina, L.G.
Skurat, E.V.
Frolova, O.Yu.
Komarova, T.V.
Karger, E.M.
Atabekov, I.G.
author_facet Tyulkina, L.G.
Skurat, E.V.
Frolova, O.Yu.
Komarova, T.V.
Karger, E.M.
Atabekov, I.G.
author_sort Tyulkina, L.G.
collection PubMed
description The novel viral vectors PVX-CP AltMV and PVXdt-CP AltMV are superexpressors of the capsid protein (CP). These viral vectors were constructed on the basis of the potato virus X (PVX) genome andAlternantheramosaic virus (AltMV) CP gene. The expression, based on the hybrid viral vectors, is genetically safe, since the systemic transport and formation of infective viral particles are blocked. CP AltMV can self-assemble into virus-like particles (VLPs) in the absence of genomic RNA. The vectors can be used for the presentation of foreign peptides (including epitopes of human pathogens) on the surface of the VLP. The N-terminal extracellular domain (M2e) of the influenza virus A M2 protein and its truncated variant (ΔM2e) were used as model heterologous peptides for the construction of the chimeric CP AltMV. Chimeric CP AltMV retains its ability to self-assemble into VLP. The epitopes of the M2 influenza virus protein were not eliminated during the process of accumulation, polymerization and purification of chimeric VLP AltMV, providing evidence of the stability of chimeric VLP with C-terminal heterologous epitopes. It appears that VLP produced by the vectors PVX-CP AltMV and PVXdt-CP AltMV can be used in the field of biotechnology for the presentation of the epitopes of vaccine proteins on their surfaces. The chimeric VLP AltMV with the presented foreign epitopes can be used as candidate vaccines.
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spelling pubmed-33476182012-05-30 New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants Tyulkina, L.G. Skurat, E.V. Frolova, O.Yu. Komarova, T.V. Karger, E.M. Atabekov, I.G. Acta Naturae Research Article The novel viral vectors PVX-CP AltMV and PVXdt-CP AltMV are superexpressors of the capsid protein (CP). These viral vectors were constructed on the basis of the potato virus X (PVX) genome andAlternantheramosaic virus (AltMV) CP gene. The expression, based on the hybrid viral vectors, is genetically safe, since the systemic transport and formation of infective viral particles are blocked. CP AltMV can self-assemble into virus-like particles (VLPs) in the absence of genomic RNA. The vectors can be used for the presentation of foreign peptides (including epitopes of human pathogens) on the surface of the VLP. The N-terminal extracellular domain (M2e) of the influenza virus A M2 protein and its truncated variant (ΔM2e) were used as model heterologous peptides for the construction of the chimeric CP AltMV. Chimeric CP AltMV retains its ability to self-assemble into VLP. The epitopes of the M2 influenza virus protein were not eliminated during the process of accumulation, polymerization and purification of chimeric VLP AltMV, providing evidence of the stability of chimeric VLP with C-terminal heterologous epitopes. It appears that VLP produced by the vectors PVX-CP AltMV and PVXdt-CP AltMV can be used in the field of biotechnology for the presentation of the epitopes of vaccine proteins on their surfaces. The chimeric VLP AltMV with the presented foreign epitopes can be used as candidate vaccines. A.I. Gordeyev 2011 /pmc/articles/PMC3347618/ /pubmed/22649706 Text en Copyright © 2011 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tyulkina, L.G.
Skurat, E.V.
Frolova, O.Yu.
Komarova, T.V.
Karger, E.M.
Atabekov, I.G.
New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants
title New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants
title_full New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants
title_fullStr New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants
title_full_unstemmed New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants
title_short New Viral Vector for Superproduction of Epitopes of Vaccine Proteins in Plants
title_sort new viral vector for superproduction of epitopes of vaccine proteins in plants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347618/
https://www.ncbi.nlm.nih.gov/pubmed/22649706
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