Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
Novartis Institutes for Biomedical Research, Novartis Campus, 4056 Basel, Switzerland.
Cell Rep. 2020 Feb 18;30(7):2321-2331.e6. doi: 10.1016/j.celrep.2020.01.081.
Mitochondrial Ca uptake depends on the mitochondrial calcium uniporter (MCU) complex, a highly selective channel of the inner mitochondrial membrane (IMM). Here, we screen a library of 44,000 non-proprietary compounds for their ability to modulate mitochondrial Ca uptake. Two of them, named MCU-i4 and MCU-i11, are confirmed to reliably decrease mitochondrial Ca influx. Docking simulations reveal that these molecules directly bind a specific cleft in MICU1, a key element of the MCU complex that controls channel gating. Accordingly, in MICU1-silenced or deleted cells, the inhibitory effect of the two compounds is lost. Moreover, MCU-i4 and MCU-i11 fail to inhibit mitochondrial Ca uptake in cells expressing a MICU1 mutated in the critical amino acids that forge the predicted binding cleft. Finally, these compounds are tested ex vivo, revealing a primary role for mitochondrial Ca uptake in muscle growth. Overall, MCU-i4 and MCU-i11 represent leading molecules for the development of MICU1-targeting drugs.
线粒体钙摄取依赖于线粒体钙单向转运体(MCU)复合物,这是一种线粒体内膜(IMM)的高选择性通道。在这里,我们筛选了一个包含 44000 个非专利化合物的文库,以确定它们调节线粒体钙摄取的能力。其中两种化合物,命名为 MCU-i4 和 MCU-i11,被证实可可靠地减少线粒体钙内流。对接模拟表明,这些分子直接结合 MCU 复合物关键元件 MICU1 中一个特定的裂隙,该元件控制通道门控。因此,在沉默或删除 MICU1 的细胞中,两种化合物的抑制作用丧失。此外,MCU-i4 和 MCU-i11 无法抑制表达关键氨基酸发生突变从而形成预测结合裂隙的 MICU1 的细胞中的线粒体钙摄取。最后,这些化合物在体外进行了测试,揭示了线粒体钙摄取在肌肉生长中的主要作用。总体而言,MCU-i4 和 MCU-i11 代表了针对 MICU1 靶向药物开发的领先分子。