| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2036366 | Cell | 2011 | 13 Pages |
SummaryDevelopment of malaria parasites within vertebrate erythrocytes requires nutrient uptake at the host cell membrane. The plasmodial surface anion channel (PSAC) mediates this transport and is an antimalarial target, but its molecular basis is unknown. We report a parasite gene family responsible for PSAC activity. We used high-throughput screening for nutrient uptake inhibitors to identify a compound highly specific for channels from the Dd2 line of the human pathogen P. falciparum. Inheritance of this compound's affinity in a Dd2 × HB3 genetic cross maps to a single parasite locus on chromosome 3. DNA transfection and in vitro selections indicate that PSAC-inhibitor interactions are encoded by two clag3 genes previously assumed to function in cytoadherence. These genes are conserved in plasmodia, exhibit expression switching, and encode an integral protein on the host membrane, as predicted by functional studies. This protein increases host cell permeability to diverse solutes.PaperFlick To view the video inline, enable JavaScript on your browser. However, you can download and view the video by clicking on the icon belowHelp with MP4 filesOptionsDownload video (12178 K)
Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (413 K)Download as PowerPoint slideHighlights► Screen identifies specific inhibitor of malaria parasite nutrient uptake ► Inhibitor targets the plasmodial surface anion channel and depends on clag3 genes ► Regulated expression of clag3 genes permits switching of channel phenotypes ► The clag3 product is exposed at the erythrocyte surface
