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Structures reveal gatekeeping of the mitochondrial Ca2+ uniporter by MICU1-MICU2
The mitochondrial calcium uniporter is a Ca2+-gated ion channel complex that controls mitochondrial Ca2+ entry and regulates cell metabolism. MCU and EMRE form the channel while Ca2+-dependent regulation is conferred by MICU1 and MICU2 through an enigmatic process. We present a cryo-EM structure of...
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description | The mitochondrial calcium uniporter is a Ca2+-gated ion channel complex that controls mitochondrial Ca2+ entry and regulates cell metabolism. MCU and EMRE form the channel while Ca2+-dependent regulation is conferred by MICU1 and MICU2 through an enigmatic process. We present a cryo-EM structure of an MCU-EMRE-MICU1-MICU2 holocomplex comprising MCU and EMRE subunits from the beetle Tribolium castaneum in complex with a human MICU1-MICU2 heterodimer at 3.3 Å resolution. With analogy to how neuronal channels are blocked by protein toxins, a uniporter interaction domain on MICU1 binds to a channel receptor site comprising MCU and EMRE subunits to inhibit ion flow under resting Ca2+ conditions. A Ca2+-bound structure of MICU1-MICU2 at 3.1 Å resolution indicates how Ca2+-dependent changes enable dynamic response to cytosolic Ca2+ signals. |
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A Ca2+-bound structure of MICU1-MICU2 at 3.1 Å resolution indicates how Ca2+-dependent changes enable dynamic response to cytosolic Ca2+ signals.</description><identifier>ISSN: 2050-084X</identifier><identifier>EISSN: 2050-084X</identifier><identifier>DOI: 10.7554/eLife.59991</identifier><identifier>PMID: 32667285</identifier><language>eng</language><publisher>Cambridge: eLife Sciences Publications Ltd</publisher><subject>Biochemistry and Chemical Biology ; Calcium (mitochondrial) ; calcium channel ; Calcium influx ; Calcium signalling ; Data collection ; gating ; ion channel ; Lipids ; membrane structure ; Mitochondria ; Proteins ; Software ; Structural Biology and Molecular Biophysics ; toxin ; tribolium castaneum</subject><ispartof>eLife, 2020-07, Vol.9</ispartof><rights>2020, Wang et al. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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MCU and EMRE form the channel while Ca2+-dependent regulation is conferred by MICU1 and MICU2 through an enigmatic process. We present a cryo-EM structure of an MCU-EMRE-MICU1-MICU2 holocomplex comprising MCU and EMRE subunits from the beetle Tribolium castaneum in complex with a human MICU1-MICU2 heterodimer at 3.3 Å resolution. With analogy to how neuronal channels are blocked by protein toxins, a uniporter interaction domain on MICU1 binds to a channel receptor site comprising MCU and EMRE subunits to inhibit ion flow under resting Ca2+ conditions. A Ca2+-bound structure of MICU1-MICU2 at 3.1 Å resolution indicates how Ca2+-dependent changes enable dynamic response to cytosolic Ca2+ signals.</abstract><cop>Cambridge</cop><pub>eLife Sciences Publications Ltd</pub><pmid>32667285</pmid><doi>10.7554/eLife.59991</doi><orcidid>https://orcid.org/0000-0002-8144-1398</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry and Chemical Biology Calcium (mitochondrial) calcium channel Calcium influx Calcium signalling Data collection gating ion channel Lipids membrane structure Mitochondria Proteins Software Structural Biology and Molecular Biophysics toxin tribolium castaneum |
title | Structures reveal gatekeeping of the mitochondrial Ca2+ uniporter by MICU1-MICU2 |
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