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Pellicle formation in the malaria parasite.
Kono, Maya; Heincke, Dorothee; Wilcke, Louisa; Wong, Tatianna Wai Ying; Bruns, Caroline; Herrmann, Susann; Spielmann, Tobias; Gilberger, Tim W.
Afiliação
  • Kono M; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany.
  • Heincke D; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany M.G. DeGroote Institute for Infectious Disease Research, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
  • Wilcke L; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany M.G. DeGroote Institute for Infectious Disease Research, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
  • Wong TW; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany M.G. DeGroote Institute for Infectious Disease Research, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
  • Bruns C; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany.
  • Herrmann S; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany M.G. DeGroote Institute for Infectious Disease Research, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
  • Spielmann T; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany.
  • Gilberger TW; Department of Cellular Parasitology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg 20359, Germany M.G. DeGroote Institute for Infectious Disease Research, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada Center for Structural Systems Bi
J Cell Sci ; 129(4): 673-80, 2016 Feb 15.
Article em En | MEDLINE | ID: mdl-26763910
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmodium falciparum / Esquizontes Limite: Humans Idioma: En Revista: J Cell Sci Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmodium falciparum / Esquizontes Limite: Humans Idioma: En Revista: J Cell Sci Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha