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• W2126672069 startingPage "4374" @default.
• W2126672069 abstract "ABSTRACT Chloroquine resistance in the malaria parasite Plasmodium falciparum is conferred by mutations in the P. falciparum c hloroquine r esistance t ransporter (PfCRT). PfCRT localizes to the membrane of the parasite's internal digestive vacuole, an acidic organelle in which chloroquine accumulates to high concentrations and exerts its toxic effect. Mutations in PfCRT are thought to reduce chloroquine accumulation in this organelle. How they do so is the subject of ongoing debate. Recently we have shown that in the presence of chloroquine there is an increased leak of H + from the digestive vacuole in chloroquine-resistant but not chloroquine-sensitive parasites. Here, using transfectant parasite strains of a single genetic background and differing only in their pfcrt allele, we show that chloroquine resistance-conferring PfCRT mutations are responsible for this chloroquine-associated H + leak. This is consistent with the hypothesis that the chloroquine resistance-conferring forms of PfCRT mediate the efflux of chloroquine, in association with H + , from the malaria parasite's digestive vacuole." @default.
• W2126672069 created "2016-06-24" @default.
• W2126672069 creator A5034570864 @default.
• W2126672069 creator A5042625619 @default.
• W2126672069 date "2008-12-01" @default.
• W2126672069 modified "2023-10-10" @default.
• W2126672069 title "Chloroquine Resistance-Conferring Mutations in <i>pfcrt</i> Give Rise to a Chloroquine-Associated H ⁺ Leak from the Malaria Parasite's Digestive Vacuole" @default.
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• W2126672069 doi "https://doi.org/10.1128/aac.00666-08" @default.
• W2126672069 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2592892" @default.
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• W2126672069 hasPublicationYear "2008" @default.
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