Trypanosoma brucei eflornithine transporter AAT6 is a low-affinity low-selective transporter for neutral amino acids

Author:

Mathieu Christoph1,Salgado Amaia González2,Wirdnam Corina1,Meier Stefan1,Grotemeyer Marianne Suter1,Inbar Ehud3,Mäser Pascal45,Zilberstein Dan3,Sigel Erwin2,Bütikofer Peter2,Rentsch Doris1

Affiliation:

1. Institute of Plant Sciences, University of Bern, Altenbergrain 21, 3013 Bern, Switzerland

2. Institute of Biochemistry and Molecular Medicine, University of Bern, Bühlstrasse 28, 3012 Bern, Switzerland

3. Faculty of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel

4. Swiss Tropical and Public Health Institute, Socinstrasse 57, 4051 Basel, Switzerland

5. University of Basel, 4000 Basel, Switzerland

Abstract

Amino acid transporters are crucial for parasite survival since the cellular metabolism of parasitic protozoa depends on the up-take of exogenous amino acids. Amino acid transporters are also of high pharmacological relevance because they may mediate uptake of toxic amino acid analogues. In the present study we show that the eflornithine transporter AAT6 from Trypanosoma brucei (TbAAT6) mediates growth on neutral amino acids when expressed in Saccharomyces cerevisiae mutants. The transport was electrogenic and further analysed in Xenopus laevis oocytes. Neutral amino acids, proline analogues, eflornithine and acivicin induced inward currents. For proline, glycine and tryptophan the apparent affinities and maximal transport rates increased with more negative membrane potentials. Proline-induced currents were dependent on pH, but not on sodium. Although proline represents the primary energy source of T. brucei in the tsetse fly, down-regulation of TbAAT6-expression by RNAi showed that in culture TbAAT6 is not essential for growth of procyclic form trypanosomes in the presence of glucose or proline as energy source. TbAAT6-RNAi lines of both bloodstream and procyclic form trypanosomes showed reduced susceptibility to eflornithine, whereas the sensitivity to acivicin remained unchanged, indicating that acivicin enters the cell by more than one transporter.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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