Cell-Based Ligand Discovery for the ENL YEATS Domain

ENL is a transcriptional coactivator that recruits elongation machinery to active cis-regulatory elements upon binding of its YEATS domaina chromatin reader moduleto acylated lysine side chains. Discovery chemistry for the ENL YEATS domain is highly motivated by its significance in acute leukemia...

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Veröffentlicht in:ACS chemical biology 2020-04, Vol.15 (4), p.895-903
Hauptverfasser: Asiaban, Joshua N, Milosevich, Natalia, Chen, Emily, Bishop, Timothy R, Wang, Justin, Zhang, Yuxiang, Ackerman, Christopher J, Hampton, Eric N, Young, Travis S, Hull, Mitchell V, Cravatt, Benjamin F, Erb, Michael A
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Sprache:eng
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Zusammenfassung:ENL is a transcriptional coactivator that recruits elongation machinery to active cis-regulatory elements upon binding of its YEATS domaina chromatin reader moduleto acylated lysine side chains. Discovery chemistry for the ENL YEATS domain is highly motivated by its significance in acute leukemia pathophysiology, but cell-based assays able to support large-scale screening or hit validation efforts do not presently exist. Here, we report on the discovery of a target engagement assay that allows for high-throughput ligand discovery in living cells. This assay is based on the cellular thermal shift assay (CETSA) but does not require exposing cells to elevated temperatures, as small-molecule ligands are able to stabilize the ENL YEATS domain at 37 °C. By eliminating temperature shifts, we developed a simplified target engagement assay that requires just two steps: drug treatment and luminescence detection. To demonstrate its value for higher throughput applications, we miniaturized the assay to a 1536-well format and screened 37 120 small molecules, ultimately identifying an acyl-lysine-competitive ENL/AF9 YEATS domain inhibitor.
ISSN:1554-8929
1554-8937
DOI:10.1021/acschembio.0c00124