Expression of influenza A virus-derived peptides on a rotavirus VP6-based delivery platform

Recombinant protein technology enables the engineering of modern vaccines composed of a carrier protein displaying poorly immunogenic heterologous antigens. One promising carrier is based on the rotavirus inner-capsid VP6 protein. We explored different VP6 insertion sites for the presentation of two...

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Bibliographic Details
Published inArchives of virology Vol. 166; no. 1; pp. 213 - 217
Main Authors Gröhn, Stina, Heinimäki, Suvi, Tamminen, Kirsi, Blazevic, Vesna
Format Journal Article
LanguageEnglish
Published Vienna Springer Vienna 01.01.2021
Springer Nature B.V
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Summary:Recombinant protein technology enables the engineering of modern vaccines composed of a carrier protein displaying poorly immunogenic heterologous antigens. One promising carrier is based on the rotavirus inner-capsid VP6 protein. We explored different VP6 insertion sites for the presentation of two peptides (23 and 140 amino acids) derived from the M2 and HA genes of influenza A virus. Both termini and three surface loops of VP6 were successfully exploited as genetic fusion sites, as demonstrated by the expression of the fusion proteins. However, further studies are needed to assess the morphology and immunogenicity of these constructs.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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Handling Editor: Reimar Johne.
ISSN:0304-8608
1432-8798
DOI:10.1007/s00705-020-04847-5