期刊
MOLECULAR AND BIOCHEMICAL PARASITOLOGY
卷 237, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.molbiopara.2020.111275
关键词
Mitochondrial carrier family; Energy metabolism; Trypanosoma brucei; Cytokinesis; Phosphate transport; Mitochondrial membrane potential
资金
- BBSRC [BB/G00448X/1]
- BBSRC [BB/G00448X/1] Funding Source: UKRI
Conserved amongst all eukaryotes is a family of mitochondrial carrier proteins (SLC25A) responsible for the import of various solutes across the inner mitochondrial membrane. We previously reported that the human parasite Trypanosoma brucei possesses 26 SLC25A proteins (TbMCPs) amongst which two, TbMCP11 and TbMCP8, were predicted to function as phosphate importers. The transport of inorganic phosphate into the mitochondrion is a prerequisite to drive ATP synthesis by substrate level and oxidative phosphorylation and thus crucial for cell viability. In this paper we describe the functional characterization of TbMCP11. In procyclic form T. brucei, the RNAi of TbMCP11 blocked ATP synthesis on mitochondrial substrates, caused a drop of the mitochondrial oxygen consumption and drastically reduced cell viability. The functional complementation in yeast and mitochondrial swelling experiments suggested a role for TbMCP11 as inorganic phosphate carrier. Interestingly, procyclic form T. brucei cells in which TbMCP11 was depleted displayed an inability to either replicate or divide the kinetoplast DNA, which resulted in a severe cytokinesis defect.
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