Abstract
A recombinant baculovirus capable of expressing the glycoprotein H (gH) gene of equine herpesvirus 1 (EHV-1) was constructed. EHV-1 gH gene products in recombinant baculovirus infected insect cells were identified as 105 kDa and 110 kDa species compared with a 115 kDa product detected in EHV-1 infected mammalian cells. The extent of N-glycosylation of EHV-1 gH in both insect and mammalian cells was indicated by a shift in apparent molecular weights after PNGase F treatment to 90 kDa and 95 kDa forms, which compared with the predicted value of 90 kDa for the unglycosylated polypeptide. The recombinant EHV-1 gH was recognised by equine sera demonstrating that EHV-1 gH is a target for the immune system of the natural host. However, while the recombinant EHV-1 gH product from infected insect cells was immunogenic in mice, it did not induce a neutralizing antibody response against EHV-1. © 1994 Springer-Verlag.
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CITATION STYLE
McGowan, E. M., Hayden, M. B., Edwards, S. J., Pye, D., Love, D. N., & Whalley, J. M. (1994). Expression and characterisation of equine herpesvirus 1 glycoprotein H using a recombinant baculovirus. Archives of Virology, 137(3–4), 389–395. https://doi.org/10.1007/BF01309484
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