Defining the role of PfCRT in Plasmodium falciparum chloroquine resistance

Patrick G. Bray, Rowena E. Martin, Leann Tilley, Stephen A. Ward, Kiaran Kirk, David A. Fidock*

*Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    161 Citations (Scopus)

    Abstract

    Recent studies have highlighted the importance of a parasite protein referred to as the chloroquine resistance transporter (PfCRT) in the molecular basis of Plasmodium falciparum resistance to the quinoline antimalarials. PfCRT, an integral membrane protein with 10 predicted transmembrane domains, is a member of the drug/metabolite transporter super-family and is located on the membrane of the intra-erythrocytic parasite's digestive vacuole. Specific polymorphisms in PfCRT are tightly correlated with chloroquine resistance. Transfection studies have now proven that pfcrt mutations confer verapamil-reversible chloroquine resistance in vitro and reveal their important role in resistance to quinine. Available evidence is consistent with the view that PfCRT functions as a transporter directly mediating the efflux of chloroquine from the digestive vacuole.

    Original languageEnglish
    Pages (from-to)323-333
    Number of pages11
    JournalMolecular Microbiology
    Volume56
    Issue number2
    DOIs
    Publication statusPublished - Mar 2005

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