Substitution of amino acid residue in influenza A virus hemagglutinin affects recognition of sialyl-oligosaccharides containing N-glycolylneuraminic acid

FEBS Lett. 1999 Dec 24;464(1-2):71-4. doi: 10.1016/s0014-5793(99)01575-6.

Abstract

Sialic acids are essential components of cell surface receptors used by influenza viruses. To determine the molecular mechanisms of viral recognition of two major species of sialic acids, N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc), we tested the binding reactivity of nine human H3 influenza A viruses to sialylglycolipids containing type II sugar chain and different molecular species of terminal sialic acids. All human H3 viruses tested except A/Memphis/1/71 bound both Neu5Ac and Neu5Gc. Nucleotide sequence analysis suggests that amino acids at 143, 155, and 158 are linked to the viral recognition of Neu5Gc.

MeSH terms

  • Amino Acid Sequence
  • Carbohydrate Sequence
  • Chromatography, Thin Layer
  • Glycoconjugates / metabolism
  • Hemagglutinins / chemistry*
  • Humans
  • Influenza A virus / chemistry*
  • Models, Molecular
  • Molecular Sequence Data
  • Neuraminic Acids / metabolism*
  • Sequence Homology, Amino Acid
  • Sialoglycoproteins / metabolism*
  • Viral Proteins / metabolism

Substances

  • Glycoconjugates
  • Hemagglutinins
  • Neuraminic Acids
  • Sialoglycoproteins
  • Viral Proteins
  • N-glycolylneuraminic acid