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In vivo studies support the role of trafficking and cytoskeletal-binding motifs in the interaction of MESA with the membrane skeleton of Plasmodium falciparum-infected red blood cells

  • Casilda Gabrielle Black
  • , Nicholas Ian Proellocks
  • , Lev Kats
  • , Brian Mark Cooke
  • , Narla Mohandas
  • , Ross Leon Coppel

Research output: Contribution to journalArticleResearchpeer-review

Abstract

In red blood cells (RBCs) infected with the malaria parasite Plasmodium falciparum, a 19-residue region of the mature parasite-infected erythrocyte surface antigen (MESA) associates with RBC cytoskeleton protein 4.1R; an interaction essential for parasite survival. This region in MESA is adjacent to a host targeting motif found in other malaria parasite proteins exported to the membrane skeleton. To demonstrate function of these motifs in vivo, regions of MESA fused to a reporter were expressed in malaria parasites. Immunochemical analyses confirmed the requirement for both motifs in the trafficking and interaction of MESA with the cytoskeleton and demonstrates their function in vivo.
Original languageEnglish
Pages (from-to)143 - 147
Number of pages5
JournalMolecular and Biochemical Parasitology
Volume160
Issue number2
Publication statusPublished - 2008

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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