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Projekt Druckansicht

Ein Lipocalin als potenzieller Regulator von Hämoglobinabbau und Hämozoinformation in der Nahrungsvakuole des Malariaparasiten

Antragsteller Dr. Joachim Michael Matz
Fachliche Zuordnung Parasitologie und Biologie der Erreger tropischer Infektionskrankheiten
Zellbiologie
Förderung Förderung von 2019 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 419345764
 
Erstellungsjahr 2022

Zusammenfassung der Projektergebnisse

During blood stage development, malaria parasites are challenged with the detoxification of enormous amounts of haem released during the proteolytic catabolism of erythrocytic haemoglobin. They tackle this problem by sequestering haem into bioinert crystals known as haemozoin. The mechanisms underlying this biomineralization process remain enigmatic. In this project, I have demonstrated that both rodent and human malaria parasite species secrete and internalize a lipocalin-like protein, PV5, to control haem crystallization. Transcriptional deregulation of PV5 in the rodent parasite Plasmodium berghei results in inordinate elongation of haemozoin crystals, while conditional PV5 inactivation in the human malaria agent Plasmodium falciparum causes excessive multi-directional crystal branching. Although haemoglobin processing remains unaffected, PV5-deficient parasites generate less haemozoin. Electron diffraction analysis indicates that despite the distinct changes in crystal morphology neither the crystalline order nor unit cell of haemozoin are affected by impaired PV5 function. Deregulation of PV5 expression renders P. berghei hypersensitive to the antimalarial drugs artesunate, chloroquine, and atovaquone, resulting in accelerated parasite clearance following drug treatment in vivo. Together, these findings demonstrate the Plasmodium-tailored role of a lipocalin family member in haemozoin formation and underscore the haem biomineralization pathway as an attractive target for therapeutic exploitation. An improved understanding of the mechanisms underlying haem sequestration will provide valuable insights for future drug development efforts.

Projektbezogene Publikationen (Auswahl)

  • A lipocalin mediates unidirectional heme biomineralization in malaria parasites. PNAS. 2020; 117:16546– 56
    Matz JM, Drepper B, Blum TB, van Genderen E, Burrell A, Martin P, Stach T, Collinson L, Abrahams JP, Matuschewski K, Blackman MJ
    (Siehe online unter https://doi.org/10.1073/pnas.2001153117)
  • The parasitophorous vacuole of the blood-stage malaria parasite. Nat Rev Microbiol. 2020; 18:379–91
    Matz JM, Beck J, Blackman MJ
    (Siehe online unter https://doi.org/10.1038/s41579-019-0321-3)
  • An apicoplast-resident folate transporter is essential for sporogony of malaria parasites. Cell Microbiol. 2021; 23:e13266
    Korbmacher F, Drepper B, Sanderson T, Martin P, Stach T, Maier AG, Matuschewski K, Matz JM
    (Siehe online unter https://doi.org/10.1111/cmi.13266)
 
 

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