In vivo studies support the role of trafficking and cytoskeletal-binding motifs in the interaction of MESA with the membrane skeleton of Plasmodium falciparum-infected red blood cells |
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Authors: | Black Casilda G Proellocks Nicholas I Kats Lev M Cooke Brian M Mohandas Narla Coppel Ross L |
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Affiliation: | NHMRC Program in Malaria, Department of Microbiology, Monash University, Victoria 3800, Australia. |
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Abstract: | In red blood cells (RBCs) infected with the malaria parasite Plasmodium falciparum, a 19-residue region of the mature parasite-infected erythrocyte surface antigen (MESA) associates with RBC cytoskeleton protein 4.1R; an interaction essential for parasite survival. This region in MESA is adjacent to a host targeting motif found in other malaria parasite proteins exported to the membrane skeleton. To demonstrate function of these motifs in vivo, regions of MESA fused to a reporter were expressed in malaria parasites. Immunochemical analyses confirmed the requirement for both motifs in the trafficking and interaction of MESA with the cytoskeleton and demonstrates their function in vivo. |
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Keywords: | Plasmodium falciparum Malaria MESA Pexel Trafficking Cytoskeleton 4.1R |
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