Interactions with heparin-like molecules during erythrocyte invasion by Plasmodium falciparum merozoites

Blood. 2010 Jun 3;115(22):4559-68. doi: 10.1182/blood-2009-09-243725. Epub 2010 Mar 10.

Abstract

During erythrocyte invasion, Plasmodium falciparum merozoites use multiple receptor-ligand interactions in a series of coordinated events, but current knowledge of these interactions is limited. Using real-time imaging of invasion, we established that heparin-like molecules block early, and essential, events in erythrocyte invasion by merozoites. All P falciparum isolates tested, and parasites using different invasion pathways were inhibited to comparable levels. Furthermore, it was not possible to select for heparin-resistant parasites. Heparin-like molecules occur naturally on the surface of human erythrocytes, where they may act as receptors for binding of merozoite surface proteins. Consistent with this, we demonstrated that MSP1-42, a processed form of merozoite surface protein 1 (MSP1) involved in invasion, bound heparin in a specific manner; furthermore, binding was observed with the secondary processing fragment MSP1-33, but not MSP1-19. We defined key structural requirements of heparin-like molecules for invasion inhibition and interactions with MSP1-42. Optimal activity required a degree of sulfation more than or equal to 2, disulfation of the N-acetylglucosamine or hexuronic acid residue, and a minimum chain length of 6 monosaccharides. These findings have significant implications for understanding P falciparum invasion of erythrocytes and the development of novel therapeutics and vaccines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Erythrocytes / metabolism*
  • Erythrocytes / parasitology*
  • Heparin / blood*
  • Heparin / chemistry
  • Host-Parasite Interactions / physiology
  • Humans
  • In Vitro Techniques
  • Merozoite Surface Protein 1 / chemistry
  • Merozoite Surface Protein 1 / physiology
  • Merozoites / physiology
  • Molecular Structure
  • Peptide Fragments / chemistry
  • Peptide Fragments / physiology
  • Plasmodium falciparum / genetics
  • Plasmodium falciparum / pathogenicity*
  • Plasmodium falciparum / physiology
  • Protein Binding
  • Protein Processing, Post-Translational
  • Receptors, Cell Surface / physiology

Substances

  • Merozoite Surface Protein 1
  • Peptide Fragments
  • Receptors, Cell Surface
  • Heparin