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• W2896001644 abstract "Lipid homeostasis is essential to the maintenance of life. We previously reported that disruptions of the parasite Na+ homeostasis via inhibition of PfATP4 resulted in elevated cholesterol within the parasite plasma membrane as assessed by saponin sensitivity. A large number of compounds have been shown to target the parasite Na+ homeostasis. We screened 800 compounds from the Malaria and Pathogen Boxes to identify chemotypes that disrupted the parasite plasma membrane lipid homeostasis. Here, we show that the compounds disrupting parasite Na+ homeostasis also induced saponin sensitivity, an indication of parasite lipid homeostasis disruption. Remarkably, 13 compounds were identified that altered the plasma membrane lipid composition independently of the Na+ homeostasis disruption. Further studies suggest that these compounds target the Plasmodium falciparum Niemann-Pick type C1-related (PfNCR1) protein, which is hypothesized to be involved in maintaining plasma membrane lipid composition. PfNCR1, like PfATP4, appears to be targeted by multiple chemotypes with the potential for drug discovery." @default.
• W2896001644 created "2018-10-26" @default.
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• W2896001644 date "2019-01-14" @default.
• W2896001644 modified "2023-10-18" @default.
• W2896001644 title "Diverse Chemical Compounds Target <i>Plasmodium falciparum</i> Plasma Membrane Lipid Homeostasis" @default.
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• W2896001644 doi "https://doi.org/10.1021/acsinfecdis.8b00277" @default.
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