Distorting malaria peptide backbone structure to enable fitting into MHC class II molecules renders modified peptides immunogenic and protective

J Med Chem. 2003 May 22;46(11):2250-3. doi: 10.1021/jm020440w.

Abstract

The conserved, nonantigenic, nonimmunogenic malaria Merozoite Surface Protein-2 peptide 1, having high affinity for red blood cells, was rendered immunogenic and protective in Aotus monkeys by specifically changing some critical residues. The NMR structure revealed a switch from classical type III' into distorted III' and III beta turns in the protective peptides. These changes may lead to a better fit into the Aotus MHC class II human HLA-DRbeta1 12 molecule equivalent, thus activating the immune system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Protozoan / chemistry*
  • Antigens, Protozoan / immunology
  • Aotidae
  • Histocompatibility Antigens Class II / immunology*
  • Magnetic Resonance Spectroscopy
  • Malaria, Falciparum / immunology
  • Malaria, Falciparum / prevention & control
  • Models, Molecular
  • Peptides / chemistry*
  • Peptides / immunology
  • Plasmodium falciparum / immunology
  • Protein Conformation
  • Protozoan Proteins / chemistry*
  • Protozoan Proteins / immunology
  • Vaccination

Substances

  • Antigens, Protozoan
  • Histocompatibility Antigens Class II
  • Peptides
  • Protozoan Proteins
  • merozoite surface protein 2, Plasmodium