Systematic Identification of MCU Modulators by Orthogonal Interspecies Chemical Screening.

نویسندگان

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

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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عنوان ژورنال:
  • Molecular cell

دوره 67 4  شماره 

صفحات  -

تاریخ انتشار 2017