Authors
A Schneider2; A Harsman2; C Wenger2; S Oeljeklaus1; J Huot2; B Warscheid1;
1 Department of Biochemistry and Functional Proteomics, Universität Freiburg, Germany; 2 Department of Chemistry and Biochemistry, Universität Bern, Switzerland
Discussion
Mitochondrial protein import is essential for all eukaryotes. Here we
show that the early diverging eukaryote Trypanosoma
brucei has a non-canonical inner membrane protein translocase (TIM) which
unlike in other systems appears to mediate import of both
presequence-containing and mitochondrial carrier proteins. We have analyzed the
composition of the trypanosomal TIM complex. Besides TbTim17, which is the
single member of the Tim17/22/23 family in trypanosomes, it contains nine
subunits that are co-purified in reciprocal immunoprecipitations and with an
import substrate that is trapped in the translocation channel. Two of the newly
discovered TIM subunits are rhomboid-like proteins, which are essential for growth
and mitochondrial protein import. Rhomboid-like proteins were proposed to form
the protein translocation pore of the ER-associated degradation system (ERAD).
No further candidates for the translocation channel are found among the
subunits of the trypanosomal TIM complex, suggesting that the rhomboid-like
proteins may contribute to pore formation.