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Journal of Virology, August 2007, p. 8367-8370, Vol. 81, No. 15
0022-538X/07/$08.00+0 doi:10.1128/JVI.00819-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Edward M. Perkins,2
Augusto Frisancho,1,
Eugene Huang,1,
and
Prashant Desai1*
Viral Oncology Program, The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins,1 Department of Biology and Integrated Imaging Center, Johns Hopkins University, Baltimore, Maryland2
Received 17 April 2007/ Accepted 14 May 2007
The herpes simplex virus (HSV) triplex is a complex of three protein subunits, VP19C and a dimer of VP23 that is essential for capsid assembly. We have derived HSV-1 recombinant viruses that contain monomeric red fluorescent protein (mRFP1), a Flu hemagglutinin (HA) epitope, and a six-histidine tag fused to the amino terminus of VP19C. These viruses were capable of growth on Vero cells, indicating that the amino terminus of VP19C could tolerate these fusions. By use of immunoelectron microscopy methods, capsids that express VP19C-mRFP but not VP19C-HA were labeled with gold particles when incubated with the corresponding antibody. Our conclusion from the data is that a large tag at the N terminus of VP19C was sufficiently exposed on the capsid surface for polyclonal antibody reactivity, while the small HA epitope was inaccessible to the antibody. These data indicate that an epitope tag at the amino terminus of VP19C is not exposed at the capsid surface for reactivity to its antibody.
Published ahead of print on 23 May 2007.
Present address: Division of Pulmonary, Allergy and Critical Care Medicine, Columbia University, New York, NY 10027.
Present address: Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205.
Present address: College of Dentistry, New York University, New York, NY 10010.
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