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基于细胞的 ENL YEATS 结构域配体发现。

Cell-Based Ligand Discovery for the ENL YEATS Domain.

机构信息

Department of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.

Calibr at Scripps Research, La Jolla, California 92037, United States.

出版信息

ACS Chem Biol. 2020 Apr 17;15(4):895-903. doi: 10.1021/acschembio.0c00124. Epub 2020 Mar 19.

Abstract

ENL is a transcriptional coactivator that recruits elongation machinery to active -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.

摘要

ENL 是一种转录共激活因子,当它的 YEATS 结构域(一种染色质读取模块)与酰化赖氨酸侧链结合时,会招募延伸机制到活性调节元件。ENL YEATS 结构域的发现化学具有高度的动机,因为它在急性白血病发病机制中具有重要意义,但目前还没有能够支持大规模筛选或命中验证工作的基于细胞的测定法。在这里,我们报告了一种靶标结合测定法的发现,该测定法允许在活细胞中进行高通量配体发现。该测定法基于细胞热转移测定法(CETSA),但不需要将细胞暴露在高温下,因为小分子配体能够在 37°C 下稳定 ENL YEATS 结构域。通过消除温度变化,我们开发了一种简化的靶标结合测定法,该测定法只需要两个步骤:药物处理和发光检测。为了证明其在更高通量应用中的价值,我们将测定法小型化到 1536 孔格式,并筛选了 37120 种小分子,最终鉴定出一种酰化赖氨酸竞争性的 ENL/AF9 YEATS 结构域抑制剂。

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