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Crystal structure of the N-terminal domain of the trypanosome flagellar protein BILBO1 reveals a ubiquitin fold with a long structured loop for protein binding.
Vidilaseris, Keni; Landrein, Nicolas; Pivovarova, Yulia; Lesigang, Johannes; Aeksiri, Niran; Robinson, Derrick R; Bonhivers, Melanie; Dong, Gang.
Afiliación
  • Vidilaseris K; Max Perutz Labs, Vienna Bio-Center, Medical University of Vienna, 1030 Vienna, Austria.
  • Landrein N; Microbiologie Fondamentale et Pathogénicité, CNRS UMR 5234, Université de Bordeaux, 33 076 Bordeaux, France.
  • Pivovarova Y; Max Perutz Labs, Vienna Bio-Center, Medical University of Vienna, 1030 Vienna, Austria.
  • Lesigang J; Max Perutz Labs, Vienna Bio-Center, Medical University of Vienna, 1030 Vienna, Austria.
  • Aeksiri N; Max Perutz Labs, Vienna Bio-Center, Medical University of Vienna, 1030 Vienna, Austria; Department of Agricultural Sciences, Naresuan University, Phitsanlolok 65000, Thailand.
  • Robinson DR; Microbiologie Fondamentale et Pathogénicité, CNRS UMR 5234, Université de Bordeaux, 33 076 Bordeaux, France.
  • Bonhivers M; Microbiologie Fondamentale et Pathogénicité, CNRS UMR 5234, Université de Bordeaux, 33 076 Bordeaux, France.
  • Dong G; Max Perutz Labs, Vienna Bio-Center, Medical University of Vienna, 1030 Vienna, Austria. Electronic address: gang.dong@meduniwien.ac.at.
J Biol Chem ; 295(6): 1489-1499, 2020 02 07.
Article en En | MEDLINE | ID: mdl-31882537
Trypanosoma brucei is a protist parasite causing sleeping sickness and nagana in sub-Saharan Africa. T. brucei has a single flagellum whose base contains a bulblike invagination of the plasma membrane called the flagellar pocket (FP). Around the neck of the FP on its cytoplasmic face is a structure called the flagellar pocket collar (FPC), which is essential for FP biogenesis. BILBO1 was the first characterized component of the FPC in trypanosomes. BILBO1's N-terminal domain (NTD) plays an essential role in T. brucei FPC biogenesis and is thus vital for the parasite's survival. Here, we report a 1.6-Å resolution crystal structure of TbBILBO1-NTD, which revealed a conserved horseshoe-like hydrophobic pocket formed by an unusually long loop. Results from mutagenesis experiments suggested that another FPC protein, FPC4, interacts with TbBILBO1 by mainly contacting its three conserved aromatic residues Trp-71, Tyr-87, and Phe-89 at the center of this pocket. Our findings disclose the binding site of TbFPC4 on TbBILBO1-NTD, which may provide a basis for rational drug design targeting BILBO1 to combat T. brucei infections.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trypanosoma brucei brucei / Ubiquitina / Flagelos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Biol Chem Año: 2020 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trypanosoma brucei brucei / Ubiquitina / Flagelos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Biol Chem Año: 2020 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Estados Unidos