| Literature DB >> 26985288 |
Natalia Milosevich1, Michael C Gignac1, James McFarlane1, Chakravarthi Simhadri1, Shanti Horvath1, Kevin D Daze1, Caitlin S Croft1, Aman Dheri1, Taylor T H Quon1, Sarah F Douglas1, Jeremy E Wulff1, Irina Paci1, Fraser Hof1.
Abstract
The polycomb paralogs CBX2, CBX4, CBX6, CBX7, and CBX8 are epigenetic readers that rely on "aromatic cage" motifs to engage their partners' methyllysine side chains. Each CBX carries out distinct functions, yet each includes a highly similar methyllysine-reading chromodomain as a key element. CBX7 is the only chromodomain that has yet been targeted by chemical inhibition. We report a small set of peptidomimetic agents in which a simple chemical modification switches the ligands from one with promiscuity across all polycomb paralogs to one that provides selective inhibition of CBX6. The structural basis for this selectivity, which involves occupancy of a small hydrophobic pocket adjacent to the aromatic cage, was confirmed through molecular dynamics simulations. Our results demonstrate the increases in affinity and selectivity generated by ligands that engage extended regions of chromodomain binding surfaces.Entities:
Keywords: CBX6; Epigenetics; Polycomb Group proteins; methyllysine reader proteins; peptidomimetics
Year: 2015 PMID: 26985288 PMCID: PMC4753544 DOI: 10.1021/acsmedchemlett.5b00378
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345