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Vol. 10, Issue 8, 2547-2557, August 1999
University of Fribourg, Institute of Zoology, Pérolles,
CH-1700 Fribourg, Switzerland
Import of tRNA into the mitochondrial matrix of Trypanosoma
brucei was reconstituted in vitro. Efficient import required
the hydrolysis of externally added ATP and was shown to be a
carrier-mediated process depending on proteinaceous receptors on the
surface of mitochondria. A partly synthetic tRNATyr as well
as a physiological tRNALys were imported along the same
pathway. Contrary to import of all matrix-localized proteins, tRNA
import does not require a membrane potential. Furthermore, addition of
an excess of import-competent tRNA had no effect on import of a
mitochondrial matrix protein. In summary, these results show that tRNAs
and proteins in T. brucei are imported by fundamentally
different mechanisms.
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