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高通量筛选鉴定 MCU1 靶向化合物。

A High-Throughput Screening Identifies MICU1 Targeting Compounds.

机构信息

Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.

Novartis Institutes for Biomedical Research, Novartis Campus, 4056 Basel, Switzerland.

出版信息

Cell Rep. 2020 Feb 18;30(7):2321-2331.e6. doi: 10.1016/j.celrep.2020.01.081.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aa4/7034061/1bdd9aeb6073/fx1.jpg

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