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The divergent N-terminal domain of Tim17 is critical for its assembly in the TIM complex in Trypanosoma brucei.
Weems, Ebony; Singha, Ujjal K; Smith, Joseph T; Chaudhuri, Minu.
Afiliación
  • Weems E; Department of Microbiology and Immunology, Meharry Medical College, Nashville, TN, 37209, United States.
  • Singha UK; Department of Microbiology and Immunology, Meharry Medical College, Nashville, TN, 37209, United States.
  • Smith JT; Department of Microbiology and Immunology, Meharry Medical College, Nashville, TN, 37209, United States.
  • Chaudhuri M; Department of Microbiology and Immunology, Meharry Medical College, Nashville, TN, 37209, United States. Electronic address: mchaudhuri@mmc.edu.
Mol Biochem Parasitol ; 218: 4-15, 2017 12.
Article en En | MEDLINE | ID: mdl-28965880
Trypanosoma brucei Tim17(TbTim17), the single member of the Tim17/23/22 protein family, is an essential component of the translocase of the mitochondrial inner membrane (TIM). In spite of the conserved secondary structure, the primary sequence of TbTim17, particularly the N-terminal hydrophilic region, is significantly divergent. In order to understand the function of this region we expressed two N-terminal deletion mutants (Δ20 and Δ30) of TbTim17 in T. brucei. Both of these mutants of TbTim17 were targeted to mitochondria, however, they failed to complement the growth defect of TbTim17 RNAi cells. In addition, the import defect of other nuclear encoded proteins into TbTim17 knockdown mitochondria were not restored by expression of the N-terminal deletion mutants but complemented by knock-in of the full-length protein. Further analysis revealed that Δ20-TbTim17 and Δ30-TbTim17 mutants were not localized in the mitochondrial inner membrane. Analysis of the protein complexes in the wild type and mutant mitochondria by two-dimensional Blue-native/SDS-PAGE revealed that none of these mutants are assembled into the TbTim17 protein complex. However, FL-TbTim17 was integrated into the mitochondrial inner membrane and assembled into TbTim17 complex. Co-immunoprecipitation analysis showed that unlike the FL-TbTim17, mutant proteins are not associated with the endogenous TbTim17 as well as its interacting partner TbTim62, a novel trypanosome specific Tim. Together, these results show that the N-terminal domain of TbTim17 plays unique and essential roles for its sorting and assembly into the TbTim17 protein complex.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trypanosoma brucei brucei / Peptidil Transferasas / Membranas Mitocondriales / Multimerización de Proteína Idioma: En Revista: Mol Biochem Parasitol Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trypanosoma brucei brucei / Peptidil Transferasas / Membranas Mitocondriales / Multimerización de Proteína Idioma: En Revista: Mol Biochem Parasitol Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Países Bajos