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PMID: 8139029 Published · ppublish English Comparative Study Journal Article

Assembly of herpes simplex virus (HSV) intermediate capsids in insect cells infected with recombinant baculoviruses expressing HSV capsid proteins.

Journal of virology ·Vol. 68 ·No. 4 ·1994-04-00 ·Pages 2442-57

Thomsen DR, Roof LL, Homa FL

Abstract

The capsid of herpes simplex virus type 1 (HSV-1) is composed of seven proteins, VP5, VP19C, VP21, VP22a, VP23, VP24, and VP26, which are the products of six HSV-1 genes. Recombinant baculoviruses were used to express the six capsid genes (UL18, UL19, UL26, UL26.5, UL35, and UL38) in insect cells. All constructs expressed the appropriate-size HSV proteins, and insect cells infected with a mixture of the six recombinant baculoviruses contained large numbers of HSV-like capsids. Capsids were purified by sucrose gradient centrifugation, and electron microscopy showed that the capsids made in Sf9 cells had the same size and appearance as authentic HSV B capsids. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis demonstrated that the protein composition of these capsids was nearly identical to that of B capsids isolated from HSV-infected Vero cells. Electron microscopy of thin sections clearly demonstrated that the capsids made in insect cells contained the inner electron-translucent core associated with HSV B capsids. In infections in which single capsid genes were left out, it was found that the UL18 (VP23), UL19 (VP5), UL38 (VP19C), and either the UL26 (VP21 and VP24) or the UL26.5 (VP22a) genes were required for assembly of 100-nm capsids. VP22a was shown to form the inner core of the B capsid, since in infections in which the UL26.5 gene was omitted the 100-nm capsids that formed lacked the inner core. The UL35 (VP26) gene was not required for assembly of 100-nm capsids, although assembly of B capsids was more efficient when it was present. These and other observations indicate that (i) the products of the UL18, UL19, UL35, and UL38 genes self-assemble into structures that form the outer surface (icosahedral shell) of the capsid, (ii) the products of the UL26 and/or UL26.5 genes are required (as scaffolds) for assembly of 100-nm capsids, and (iii) the interaction of the outer surface of the capsid with the scaffolding proteins requires the product of the UL18 gene (VP23).

MeSH Terms
Animals Blotting, Western Capsid/biosynthesis,genetics,ultrastructure Centrifugation, Density Gradient Herpesvirus 1, Human/genetics,growth & development,ultrastructure Microscopy, Electron Models, Biological Morphogenesis Moths/cytology Negative Staining Nucleopolyhedroviruses/genetics Precipitin Tests Protein Processing, Post-Translational Recombinant Proteins/biosynthesis,ultrastructure Vero Cells
Chemicals
Recombinant Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Thomsen D R
Upjohn Company, Kalamazoo, Michigan 49001.
Roof L L
Homa F L
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45 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1994-04-00
Pages
2442-57
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC236722
Subset
IM
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