Milosevich Natalia, Gignac Michael C, McFarlane James, Simhadri Chakravarthi, Horvath Shanti, Daze Kevin D, Croft Caitlin S, Dheri Aman, Quon Taylor T H, Douglas Sarah F, Wulff Jeremy E, Paci Irina, Hof Fraser
Department of Chemistry, University of Victoria , Victoria, V8W 3V6, Canada.
ACS Med Chem Lett. 2015 Dec 7;7(2):139-44. doi: 10.1021/acsmedchemlett.5b00378. eCollection 2016 Feb 11.
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.
多梳旁系同源蛋白CBX2、CBX4、CBX6、CBX7和CBX8是表观遗传阅读器,它们依靠“芳香笼”基序与伴侣的甲基赖氨酸侧链结合。每个CBX都执行独特的功能,但每个都包含一个高度相似的甲基赖氨酸阅读染色质结构域作为关键元件。CBX7是唯一已被化学抑制靶向的染色质结构域。我们报告了一小类拟肽剂,其中一个简单的化学修饰将配体从对所有多梳旁系同源蛋白都具有混杂性的配体转变为对CBX6具有选择性抑制作用的配体。通过分子动力学模拟证实了这种选择性的结构基础,该基础涉及占据芳香笼附近的一个小疏水口袋。我们的结果表明,与染色质结构域结合表面的延伸区域结合的配体可提高亲和力和选择性。