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Characterisation of TbSmee1 suggests endocytosis allows surface-bound cargo to enter the trypanosome flagellar pocket.

Daja SchichlerAntonia KonleEva-Maria SpathSina RieglerAlexandra KleinAnna SeleznevSisco JungTimothy WuppermannNoah WetterichAlyssa R BorgesElisabeth Meyer-NatusKatharina HavlicekSonia Pérez CabreraKorbinian NiedermüllerSara SajkoMaximilian DohnXenia MalzerEmily RiemerTuguldur TumurbaatarKristina Djinovic-CarugoGang DongChristian J JanzenBrooke Morriswood
Published in: Journal of cell science (2023)
All endo- and exocytosis in the African trypanosome Trypanosoma brucei occurs at a single subdomain of the plasma membrane. This subdomain, the flagellar pocket, is a small vase-shaped invagination containing the root of the cell's single flagellum. Several cytoskeleton-associated multiprotein complexes are coiled around the neck of the flagellar pocket on its cytoplasmic face. One of these, the hook complex, was proposed to affect macromolecule entry into the flagellar pocket lumen. In previous work, knockdown of the hook complex component TbMORN1 resulted in larger cargo being unable to enter the flagellar pocket. In this study, the hook complex component TbSmee1 was characterised in bloodstream form Trypanosoma brucei and was found to be essential for cell viability. TbSmee1 knockdown resulted in flagellar pocket enlargement and impaired access to the flagellar pocket membrane by surface-bound cargo, similar to depletion of TbMORN1. Unexpectedly, inhibition of endocytosis by knockdown of clathrin phenocopied TbSmee1 knockdown, suggesting that endocytic activity itself is a prerequisite for the entry of surface-bound cargo into the flagellar pocket.
Keyphrases
  • type iii
  • stem cells
  • cell therapy
  • single cell
  • multidrug resistant