期刊
FASEB JOURNAL
卷 29, 期 8, 页码 3228-3237出版社
WILEY
DOI: 10.1096/fj.15-271353
关键词
Trypanosoma brucei; electrophysiology; Xenopus laevis oocytes
资金
- Swiss National Science Foundation [CRSII3_141913/1]
- Swiss National Science Foundation (SNF) [CRSII3_141913] Funding Source: Swiss National Science Foundation (SNF)
Discovery of novel drug targetsmay lead to improved treatment of trypanosomiasis. We characterize here 2 gene products of Trypanosoma brucei that are essential for the growth of bloodstream form (BSF) parasites, as shown by RNA interference (RNAi)-mediated down-regulation of the individual mRNAs. The primary sequences of the 2 proteins-protein encoded by gene Tb927.1.4450 (TbK1) and protein encoded by gene Tb927.9.4820 (TbK2)-indicate that both belong to the family of putative, Ca2+-activated potassium channels. The proteins were expressed in Xenopus laevis oocytes and their functions investigated by use of electrophysiological techniques. Only combined expression of TbK1 and TbK2 results in the formation of sizeable currents, indicating that these proteins probably assemble into a heteromeric ion channel. The current mediated by this channel shows little time and voltage dependence and displays a permeability ratio of K+/Na+ of > 20. The known potassium channel blocker barium inhibits this channel with a half-maximal inhibitory concentration (IC50) of 98 +/- 15 mu M. The membrane potential of trypanosomes was measured with a fluorescent dye. Individual RNAi-mediated downregulation of TbK1 or TbK2 eliminates a potassium conductance in the plasma membrane of BSF. Thus, this heteromeric potassium channel is involved in the modulation of the plasma membrane potential and represents a novel drug target in T. brucei.
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