Primary structure of the major glycan from human seminal transferrin

J Protein Chem. 1994 Jan;13(1):31-6. doi: 10.1007/BF01891990.

Abstract

Human seminal transferrin (HSmT) is an iron-containing glycoprotein whose structural properties have not been adequately investigated. The carbohydrate content of the purified glycoprotein amount to 6.1%, and monosaccharide analysis revealed the major oligosaccharide moiety to be of the N-glycoside type. The carbohydrate chains were released from the iron-free form by digestion with peptide N-glycosidase F (PNGase F) in the presence of detergents such as SDS and beta-octylglucoside. After ethanol precipitation and fractionation on Bio-Gel P-6 and Bio-Gel P-2, the oligosaccharide was further purified on Mono-Q and desalted on Bio-Gel P-2. By 600-MHz 1H-NMR spectroscopy, the primary structure of the major N-linked oligosaccharide component was established to be: [formula: see text]

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases
  • Carbohydrate Conformation
  • Carbohydrate Sequence
  • Detergents
  • Humans
  • Hydrogen
  • Magnetic Resonance Spectroscopy / methods
  • Male
  • Molecular Sequence Data
  • Oligosaccharides / chemistry*
  • Oligosaccharides / isolation & purification
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
  • Polysaccharides / chemistry*
  • Polysaccharides / isolation & purification
  • Semen / chemistry*
  • Transferrin / chemistry*
  • Transferrin / isolation & purification

Substances

  • Detergents
  • Oligosaccharides
  • Polysaccharides
  • Transferrin
  • Hydrogen
  • Amidohydrolases
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase