|
|
||||||||

Molecular Virology Group, Department of Microbiology, University of Leeds, Leeds LS2 9JT, U.K.
A portion of equine herpesvirus type 1 (EHV-1) gene 28, which is homologous to herpes simplex virus type 1 gene UL32, was expressed using a prokaryotic system to yield a fusion protein which reacted on Western blots with P19, a monoclonal antibody (MAb) that reacts with EHV-1 glycoprotein 300 (gp300), confirming that this gene encodes gp300. Hydrophobicity analysis showed that gp300 is a glycoprotein with multiple hydrophobic domains that might interact with, or span, the membrane several times. As such, it may represent the first member of a new family of herpesvirus glycoproteins to be identified as a virus structural component. Gp300 was also shown to be modified by palmitic acid residues, and a second MAb (1G12) directed against gp300 inhibited fusion between EHV-1-infected cells.
Present address: Department of Oral Biology, Leeds Dental Institute, University of Leeds, Leeds LS2 9LU, U.K.
Received 15 June 1992;
accepted 30 July 1992.
This article has been cited by other articles:
![]() |
J.-a. Huang, N. Ficorilli, C. A. Hartley, G. P. Allen, and M. J. Studdert Polymorphism of open reading frame 71 of equine herpesvirus-4 (EHV-4) and EHV-1 J. Gen. Virol., March 1, 2002; 83(3): 525 - 531. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |