S acylation of the hemagglutinin of influenza viruses: mass spectrometry reveals site-specific attachment of stearic acid to a transmembrane cysteine

J Virol. 2008 Sep;82(18):9288-92. doi: 10.1128/JVI.00704-08. Epub 2008 Jul 2.

Abstract

S acylation of cysteines located in the transmembrane and/or cytoplasmic region of influenza virus hemagglutinins (HA) contributes to the membrane fusion and assembly of virions. Our results from using mass spectrometry (MS) show that influenza B virus HA possessing two cytoplasmic cysteines contains palmitate, whereas HA-esterase-fusion glycoprotein of influenza C virus having one transmembrane cysteine is stearoylated. HAs of influenza A virus having one transmembrane and two cytoplasmic cysteines contain both palmitate and stearate. MS analysis of recombinant viruses with deletions of individual cysteines, as well as tandem-MS sequencing, revealed the surprising result that stearate is exclusively attached to the cysteine positioned in the transmembrane region of HA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Amino Acid Sequence
  • Animals
  • Cysteine / chemistry*
  • Cysteine / metabolism
  • Gammainfluenzavirus / chemistry
  • Gammainfluenzavirus / metabolism*
  • Hemagglutinin Glycoproteins, Influenza Virus / chemistry*
  • Hemagglutinin Glycoproteins, Influenza Virus / metabolism*
  • Influenza A virus / chemistry
  • Influenza A virus / metabolism*
  • Influenza B virus / chemistry
  • Influenza B virus / metabolism*
  • Molecular Sequence Data
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Stearic Acids / chemistry*
  • Stearic Acids / metabolism

Substances

  • Hemagglutinin Glycoproteins, Influenza Virus
  • Stearic Acids
  • hemagglutinin, human influenza A virus
  • stearic acid
  • Cysteine