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一种针对 NAD 依赖性酶抑制剂的聚焦 DNA 编码化学库的发现。

A Focused DNA-Encoded Chemical Library for the Discovery of Inhibitors of NAD-Dependent Enzymes.

机构信息

Department of Medicinal Chemistry , University of Utah , 30 S 2000 E , Salt Lake City , Utah 84112 , United States.

Department of Internal Medicine , University of Utah , 500 Foothill Drive , Salt Lake City , Utah 84148 , United States.

出版信息

J Am Chem Soc. 2019 Apr 3;141(13):5169-5181. doi: 10.1021/jacs.8b08039. Epub 2019 Mar 19.

Abstract

DNA-encoded chemical libraries are increasingly used in pharmaceutical research because they enable the rapid discovery of synthetic protein ligands. Here we explored whether target-class focused DNA-encoded chemical libraries can be cost-effective tools to achieve robust screening productivity for a series of proteins. The study revealed that a DNA-encoded library designed for NAD-binding pockets (NADEL) effectively sampled the chemical binder space of enzymes with ADP-ribosyltransferase activity. The extracted information directed the synthesis of inhibitors for several enzymes including PARP15 and SIRT6. The high dissimilarity of NADEL screening fingerprints for different proteins translated into inhibitors that showed selectivity for their target. The discovery of patterns of enriched structures for six out of eight tested proteins is remarkable for a library of 58 302 DNA-tagged structures and illustrates the prospect of focused DNA-encoded libraries as economic alternatives to large library platforms.

摘要

DNA 编码化学库在药物研究中越来越多地被使用,因为它们能够快速发现合成蛋白配体。在这里,我们探索了针对目标类别的 DNA 编码化学库是否可以成为实现一系列蛋白质强大筛选生产力的具有成本效益的工具。研究表明,为 NAD 结合口袋(NADEL)设计的 DNA 编码文库能够有效地对具有 ADP-核糖基转移酶活性的酶的化学结合物空间进行采样。提取的信息指导了几种酶抑制剂的合成,包括 PARP15 和 SIRT6。不同蛋白质的 NADEL 筛选指纹之间的高度不相似性转化为对其靶标具有选择性的抑制剂。对于一个包含 58302 个 DNA 标记结构的文库来说,对八种测试蛋白质中的六种进行富集结构模式的发现是显著的,这说明了聚焦 DNA 编码文库作为大型文库平台的经济替代方案的前景。

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