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Plasmodium, the causative agent of malaria, exports many proteins to the surface of the infected red blood cell (iRBC) in order to modify it toward a structure more suitable for parasite development and survival. One such exported protein, SURFIN4.2, from the parasite of human malignant malaria, P. falciparum, was identified in the trypsin-cleaved protein fraction from the iRBC surface, and is thereby inferred to be exposed on the iRBC surface. SURFIN4.2 also localize to Maurer's clefts-parasite-derived membranous structures established in the RBC cytoplasm and tethered to the RBC membrane-and their role in trafficking suggests that they are a pathway for SURFIN4.2 transport to the iRBC surface. It has not been determined the participation of protein domains and motifs within SURFIN4.2 in transport from Maurer's clefts to the iRBC surface; and herein we examined if the SURFIN4.2 intracellular region containing tryptophan-rich (WR) domain is required for its exposure on the iRBC surface.

tropical medicine and health

The Cytoplasmic Region of &lt;i&gt;Plasmodium falciparum&lt;/i&gt; SURFIN&lt;sub&gt;4.2&lt;/sub&gt; Is Required for Transport from Maurer’s Clefts to the Red Blood Cell Surface