The twists and turns of Maurer's cleft trafficking in P. falciparum-infected erythrocytes

Leann Tilley*, Rachid Sougrat, Trevor Lithgow, Eric Hanssen

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    64 Scopus citations


    The malaria parasite, Plasmodium falciparum, invades the red blood cells (RBCs) of its human host and initiates a series of morphological rearrangements within the host cell cytoplasm. The mature RBC has no endogenous trafficking machinery; therefore, the parasite generates novel structures to mediate protein transport. These include compartments called the Maurer's clefts (MC), which play an important role in the trafficking of parasite proteins to the surface of the host cell. Recent electron tomography studies have revealed MC as convoluted flotillas of flattened discs that are tethered to the RBC membrane, prompting speculation that the MC could, in one respect, represent an extracellular equivalent of the Golgi apparatus. Visualization of both resident and cargo proteins has helped decipher the signals and routes for trafficking of parasite proteins to the MC and beyond.

    Original languageEnglish (US)
    Pages (from-to)187-197
    Number of pages11
    Issue number2
    StatePublished - Feb 1 2008


    • Electron tomography
    • Green fluorescent protein
    • Maurer's clefts
    • Plasmodium falciparum
    • Protein trafficking

    ASJC Scopus subject areas

    • Structural Biology
    • Biochemistry
    • Molecular Biology
    • Genetics
    • Cell Biology


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