Characterization of a diagnostic Fab fragment binding trimeric Lewis X

Proteins. 2009 Aug 1;76(2):439-47. doi: 10.1002/prot.22356.

Abstract

Lewis X trisaccharides normally function as essential cell-cell interaction mediators. However, oligomers of Lewis X trisaccharides expressed by the parasite Schistosoma mansoni seem to be related to its evasion of the immune response of its human host. Here we show that monoclonal antibody 54-5C10-A, which is used to diagnose schistosomiasis in humans, interacts with oligomers of at least three Lewis X trisaccharides, but not with monomeric Lewis X. We describe the sequence and the 2.5 A crystal structure of its Fab fragment and infer a possible mode of binding of the polymeric Lewis X from docking studies. Our studies indicate a radically different mode of binding compared to Fab 291-2G3-A, which is specific for monomeric Lewis X, thus providing a structural explanation of the diagnostic success of 54-5C10-A.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Monoclonal / immunology
  • Binding Sites
  • Crystallography, X-Ray
  • Humans
  • Immunoglobulin Fab Fragments / chemistry*
  • Immunoglobulin Fab Fragments / immunology
  • Lewis X Antigen / analogs & derivatives
  • Mice
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Conformation
  • Sequence Alignment
  • Surface Plasmon Resonance
  • Trisaccharides / chemistry*
  • Trisaccharides / immunology*

Substances

  • Antibodies, Monoclonal
  • Immunoglobulin Fab Fragments
  • Lewis X Antigen
  • Trisaccharides
  • galactosyl-(1,4)-fucopyranosyl-(1,3)-N-acetylglucosamine

Associated data

  • GENBANK/AM944590
  • GENBANK/AM944591
  • PDB/2VQ1