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Pellicle formation in the malaria parasite
Author(s) -
Maya Kono,
Dorothee Heincke,
Louisa Wilcke,
Tatianna Wai Ying Wong,
C. Bruns,
Susann Herrmann,
Tobias Spielmann,
TimWolf Gilberger
Publication year - 2016
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.181230
Subject(s) - biology , schizogony , plasmodium falciparum , microbiology and biotechnology , organelle , membrane protein , transmembrane protein , rhoptry , basal (medicine) , membrane , immunology , malaria , biochemistry , apicomplexa , receptor , endocrinology , insulin
The intraerythrocytic developmental cycle of Plasmodium falciparum is completed with the release of up to 32 invasive daughter cells, the merozoites, into the blood stream. Before release, the final step of merozoite development is the assembly of the cortical pellicle, a multi-layered membrane structure. This unique apicomplexan feature includes the inner membrane complex (IMC) and the parasite's plasma membrane. A dynamic ring structure, referred to as the basal complex, is part of the IMC and helps to divide organelles and abscises in the maturing daughter cells. Here, we analyze the dynamics of the basal complex of P. falciparum. We report on a novel transmembrane protein of the basal complex termed BTP1, which is specific to the genus Plasmodium. It colocalizes with the known basal complex marker protein MORN1 and shows distinct dynamics as well as localization when compared to other IMC proteins during schizogony. Using a parasite plasma membrane marker cell line, we correlate dynamics of the basal complex with the acquisition of the maternal membrane. We show that plasma membrane invagination and IMC propagation are interlinked during the final steps of cell division.

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