3 results match your criteria: "ULB-Institute of Molecular Biology and Medicine[Affiliation]"

Article Synopsis
  • Actin levels are similar in both bloodstream and procyclic forms of Trypanosoma brucei, but its location and function vary significantly.
  • In bloodstream forms, actin is crucial for cell division and endocytic processes, with its depletion leading to cell death due to disrupted vesicular traffic.
  • In contrast, while procyclic forms do not rely on actin for growth, its absence causes changes in the Golgi structure without affecting the flagellar pocket.
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The life cycle of African trypanosomes is characterized by the alternation of proliferative and quiescent stages but the molecular details of this process remain unknown. Here, we describe a new cytoplasmic protein kinase from Trypanosoma brucei, termed TBPK50, that belongs to a family of protein kinases involved in the regulation of the cell cycle, cell shape and proliferation. TBPK50 is expressed only in proliferative forms but is totally absent in quiescent cells despite the fact that the gene is constitutively transcribed at the same level throughout the life cycle.

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N-linked glycans containing linear poly-N-acetyllactosamine as sorting signals in endocytosis in Trypanosoma brucei.

Curr Biol

October 1999

Laboratory of Molecular Parasitology, ULB - Institute of Molecular Biology and Medicine, 12 Rue des Professeurs Jeener et Brachet, B-6041,Gosselies, Belgium.

African trypanosomes, such as Trypanosoma brucei, are protozoan parasites that are transmitted by the tsetse fly and cause sleeping sickness in humans and Nagana in cattle. Trypanosomes evade the immune responses of their hosts by varying their surface coat protein (VSG) and restricting exocytosis and endocytosis to an invagination of the plasma membrane called the flagellar pocket (FP). The FP represents only 0.

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