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Leucine zipper-EF-hand containing transmembrane protein 1 (LETM1) forms a Ca(2+)/H(+) antiporter.


ABSTRACT: 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.

SUBMITTER: Shao J 

PROVIDER: S-EPMC5037442 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

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Leucine zipper-EF-hand containing transmembrane protein 1 (LETM1) forms a Ca<sup>2+</sup>/H<sup>+</sup> antiporter.

Shao Juan J   Fu Zhenglin Z   Ji Yanli Y   Guan Xiangchen X   Guo Shang S   Ding Zhanyu Z   Yang Xue X   Cong Yao Y   Shen Yuequan Y  

Scientific reports 20160927


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<sup>2+</sup> level in HeLa cells, respectively. Also the residue Glu221 of mouse LETM1 is identified to be necessary for Ca<sup>2+</sup> flux. The mutat  ...[more]

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