Isolation and partial chemical characterization of a 64,000-dalton glycoprotein of human cytomegalovirus

J Virol. 1984 Jan;49(1):279-82. doi: 10.1128/JVI.49.1.279-282.1984.

Abstract

A guanidinium chloride extract of [3H]glucosamine- and [35S]methionine-labeled virions plus dense bodies of human cytomegalovirus (Towne) was separated by reverse-phase high-pressure liquid chromatography. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the eluate revealed the major peak to be a glycoprotein with a relative mass of 64,000. This glycoprotein (HCMVgp64) was characterized by amino acid analysis and a high-pressure liquid chromatographic map of its tryptic peptides.

Publication types

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

MeSH terms

  • Amino Acids / analysis
  • Chromatography, High Pressure Liquid
  • Cytomegalovirus / analysis*
  • Glycoproteins / isolation & purification
  • Molecular Weight
  • Viral Proteins / isolation & purification*

Substances

  • Amino Acids
  • Glycoproteins
  • Viral Proteins