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Isoform-Selective ATAD2 Chemical Probe with Novel Chemical Structure and Unusual Mode of Action.
- Source :
-
ACS chemical biology [ACS Chem Biol] 2017 Nov 17; Vol. 12 (11), pp. 2730-2736. Date of Electronic Publication: 2017 Oct 24. - Publication Year :
- 2017
-
Abstract
- ATAD2 (ANCCA) is an epigenetic regulator and transcriptional cofactor, whose overexpression has been linked to the progress of various cancer types. Here, we report a DNA-encoded library screen leading to the discovery of BAY-850, a potent and isoform selective inhibitor that specifically induces ATAD2 bromodomain dimerization and prevents interactions with acetylated histones in vitro, as well as with chromatin in cells. These features qualify BAY-850 as a chemical probe to explore ATAD2 biology.
- Subjects :
- ATPases Associated with Diverse Cellular Activities chemistry
Cell Line, Tumor
Chromatin metabolism
DNA-Binding Proteins chemistry
Drug Discovery
Histones metabolism
Humans
Ligands
Models, Molecular
Protein Isoforms antagonists & inhibitors
Protein Isoforms chemistry
Protein Isoforms metabolism
ATPases Associated with Diverse Cellular Activities antagonists & inhibitors
ATPases Associated with Diverse Cellular Activities metabolism
DNA-Binding Proteins antagonists & inhibitors
DNA-Binding Proteins metabolism
Molecular Probes chemistry
Molecular Probes pharmacology
Protein Interaction Maps drug effects
Protein Multimerization drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1554-8937
- Volume :
- 12
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- ACS chemical biology
- Publication Type :
- Academic Journal
- Accession number :
- 29043777
- Full Text :
- https://doi.org/10.1021/acschembio.7b00708