Leucine zipper-EF-hand-containing transmembrane protein1 (LETM1) is located in the mitochondrial inner membrane and is defective in Wolf-Hirschhorn syndrome. LETM1 contains only one transmembrane helix, but it behaves as a putative transporter. Our data shows that LETM1 knockdown or overexpression robustly increases or decreases mitochondrial Ca 2+ level in HeLa cells, respectively. Also the residue Glu221 of mouse LETM1 is identified to be necessary for Ca 2+ flux. The mutation of Glu221 to glutamine abolishes the Ca 2+ -transport activity of LETM1 in cells. Furthermore, the purified LETM1 exhibits Ca 2+ /H + anti-transport activity and the activity is enhanced as the proton gradient is increased. More importantly, electron microscopy studies reveal a hexameric LETM1 with a central cavity and also, observe two different conformational states under alkaline and acidic conditions, respectively. Our results indicate that LETM1 is a Ca 2+ /H + antiporter and most likely responsible for mitochondrial Ca 2+ output.
No takes yet. Share an insight, caveat, or question.
Shao et al. (2016) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: