Close topographical relationship in alpha foetoprotein (AFP) between a lens culinaris binding glycan and the epitope recognized by AFP-reactive monoclonal antibody, 18H4

Br J Cancer. 1987 Feb;55(2):147-52. doi: 10.1038/bjc.1987.30.

Abstract

Monoclonal antibodies 18H4 and 19F12 against alpha-foetoprotein (AFP) were examined by enzyme immunoassay for binding to two forms of AFP that were separated on the basis of the reactivity with lentil lectin (LCA). LCA-binding and LCA non-binding AFP, coated on a solid phase, reacted with 18H4 but reactivity with the LCA-binding species was inhibited by 60% following pretreatment of the AFP with LCA. The lectin was a very poor inhibitor of binding of 18H4 to the AFP which did not interact with LCA. In an alternative binding assay, a polyclonal anti-AFP coated solid phase was reacted with beta-galactosidase-labelled 18H4. Pre-treatment with LCA of the LCA-reactive AFP gave 56% inhibition of binding of conjugated 18H4 while little inhibition was achieved with the LCA-nonreactive AFP component. These findings show that the epitope recognised by 18H4 is distinct from the glycan sequence that is reactive with LCA. However, the LCA-binding oligosaccharides occur in close proximity to the 18H4 epitope in the native AFP.

MeSH terms

  • Antibodies, Monoclonal
  • Binding, Competitive
  • Carcinoma, Hepatocellular / blood*
  • Dose-Response Relationship, Immunologic
  • Epitopes / analysis*
  • Humans
  • Immunoenzyme Techniques
  • Lectins / metabolism*
  • Liver Neoplasms / blood*
  • Plant Lectins*
  • alpha-Fetoproteins / immunology*
  • alpha-Fetoproteins / metabolism

Substances

  • Antibodies, Monoclonal
  • Epitopes
  • Lectins
  • Plant Lectins
  • alpha-Fetoproteins
  • lentil lectin