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Development of novel cellular histone-binding and chromatin-displacement assays for bromodomain drug discovery.

Yanai ZhanMaria Kost-AlimovaXi ShiElisabetta LeoJennifer P BardenhagenHannah E ShepardSrikanth AppikondaBhavatarini VangamudiShuping ZhaoTrang N TieuShiming JiangTimothy P HeffernanJoseph R MarszalekCarlo ToniattiGiulio DraettaJessica TylerMichelle BartonPhilip JonesWylie S PalmerMary K Geck DoJannik N Andersen
Published in: Epigenetics & chromatin (2015)
In summary, we have developed two novel complementary and cell-based drug-target engagement assays, expanding the repertoire of pharmacodynamic assays for bromodomain tool compound development. These assays have been validated through a successful TRIM24 bromodomain inhibitor program, where a micromolar lead molecule (IACS-6558) was optimized using cell-based assays to yield the first single-digit nanomolar TRIM24 inhibitor (IACS-9571). Altogether, the assay platforms described herein are poised to accelerate the discovery and development of novel chemical probes to deliver on the promise of epigenetic-based therapies.
Keyphrases
  • high throughput
  • single cell
  • drug discovery
  • dna methylation
  • small molecule
  • cell therapy
  • genome wide
  • social media
  • stem cells
  • machine learning
  • single molecule