Systematic Identification of MCU Modulators by Orthogonal Interspecies Chemical Screening

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Arduino, Daniela | Wettmarshausen, Jennifer | Vais, Horia | Navas-Navarro, Paloma | Cheng, Yiming | Leimpek, Anja | Ma, Zhongming | Delrio-Lorenzo, Alba | Giordano, Andrea | Garcia-Perez, Cecilia | Médard, Guillaume | Kuster, Bernhard | García-Sancho, Javier | Mokranjac, Dejana | Foskett, J Kevin | Alonso, M Teresa | Perocchi, Fabiana | Foskett, J. Kevin | Alonso, M. Teresa

Edité par CCSD ; Cell Press -

International audience. The mitochondrial calcium uniporter complex is essential for calcium (Ca2+) uptake into mitochondria of all mammalian tissues, where it regulates bioenergetics, cell death, and Ca2+ signal transduction. Despite its involvement in several human diseases, we currently lack pharmacological agents for targeting uniporter activity. Here we introduce a high-throughput assay that selects for human MCU-specific small-molecule modulators in primary drug screens. Using isolated yeast mitochondria, reconstituted with human MCU, its essential regulator EMRE, and aequorin, and exploiting a D-lactate- and mannitol/sucrose-based bioenergetic shunt that greatly minimizes false-positive hits, we identify mitoxantrone out of more than 600 clinically approved drugs as a direct selective inhibitor of human MCU. We validate mitoxantrone in orthogonal mammalian cell-based assays, demonstrating that our screening approach is an effective and robust tool for MCU-specific drug discovery and, more generally, for the identification of compounds that target mitochondrial functions.

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