Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA.
Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Nature. 2020 Jun;582(7810):129-133. doi: 10.1038/s41586-020-2309-6. Epub 2020 May 20.
Mitochondria take up Ca through the mitochondrial calcium uniporter complex to regulate energy production, cytosolic Ca signalling and cell death. In mammals, the uniporter complex (uniplex) contains four core components: the pore-forming MCU protein, the gatekeepers MICU1 and MICU2, and an auxiliary subunit, EMRE, essential for Ca transport. To prevent detrimental Ca overload, the activity of MCU must be tightly regulated by MICUs, which sense changes in cytosolic Ca concentrations to switch MCU on and off. Here we report cryo-electron microscopic structures of the human mitochondrial calcium uniporter holocomplex in inhibited and Ca-activated states. These structures define the architecture of this multicomponent Ca-uptake machinery and reveal the gating mechanism by which MICUs control uniporter activity. Our work provides a framework for understanding regulated Ca uptake in mitochondria, and could suggest ways of modulating uniporter activity to treat diseases related to mitochondrial Ca overload.
线粒体通过线粒体钙单向转运体复合物摄取 Ca2+,以调节能量产生、细胞溶质 Ca2+信号转导和细胞死亡。在哺乳动物中,单向转运体复合物(uniplex)包含四个核心成分:形成孔的 MCU 蛋白、门控蛋白 MICU1 和 MICU2 以及辅助亚基 EMRE,这对于 Ca2+转运是必需的。为了防止有害的 Ca2+过载,MCU 的活性必须由 MICUs 严格调节,MICUs 可以感应细胞溶质 Ca2+浓度的变化,从而开启和关闭 MCU。在这里,我们报告了人线粒体钙单向转运体全复合物在抑制和 Ca2+激活状态下的冷冻电镜结构。这些结构定义了这种多组分 Ca2+摄取机制的结构,并揭示了 MICUs 控制单向转运体活性的门控机制。我们的工作为理解线粒体中受调控的 Ca2+摄取提供了一个框架,并可能为调节单向转运体活性以治疗与线粒体 Ca2+过载相关的疾病提供思路。