Characterization of the large tegument protein (ICP1/2) of herpes simplex virus type 1

Virology. 1992 Sep;190(1):221-32. doi: 10.1016/0042-6822(92)91208-c.

Abstract

ICP1/2 (also designated VP1/2) is a 270-kDa structural protein of herpes simplex virus type 1 (HSV-1) which is located in the tegument region of the virion. In this report we describe the production of a polyclonal antiserum specific for ICP1/2 and the use of this antiserum to examine the synthesis, processing, and intracellular localization of the viral polypeptide. Pulse-labeling studies indicated that ICP1/2 is synthesized late during infection, being initially detectable between 8 and 9 hr postinfection with the rate of synthesis continuing to increase until 11 to 12 hr postinfection. Further studies on the expression of ICP1/2 in the presence or absence of viral DNA replication indicated that the synthesis of the polypeptide is absolutely dependent on viral DNA replication. These results suggest that ICP1/2 represents a gamma 2 (true late) gene product. Additionally, we have performed experiments to determine if ICP1/2 is post-translationally modified in HSV-infected cells. These studies indicated that ICP1/2 is phosphorylated on serine residues; however, we found no evidence to suggest that the protein is glycosylated. Using subcellular fractionation and indirect immunofluorescence techniques, we have determined that ICP1/2 is diffusely distributed throughout the nucleus and cytoplasm of HSV-infected cells with no specific compartmentalization of the polypeptide.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibody Specificity
  • Cell Compartmentation
  • Cell Fractionation
  • Cell Line
  • Glycosylation
  • Humans
  • Immune Sera / immunology
  • Kinetics
  • Phosphorylation
  • Simplexvirus / chemistry
  • Simplexvirus / immunology
  • Simplexvirus / metabolism*
  • Viral Structural Proteins / biosynthesis
  • Viral Structural Proteins / immunology
  • Viral Structural Proteins / metabolism*

Substances

  • Immune Sera
  • Viral Structural Proteins