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一种小分子探针,通过荧光偏振监测与脯氨酰羟化酶结构域 2 的结合。

A small-molecule probe for monitoring binding to prolyl hydroxylase domain 2 by fluorescence polarisation.

机构信息

Laboratory of Drug Design and Discovery, Department of Chemistry, China Pharmaceutical University, Nanjing 211198, China.

出版信息

Chem Commun (Camb). 2020 Nov 25;56(91):14199-14202. doi: 10.1039/d0cc06353c. Epub 2020 Oct 28.

Abstract

Inhibition of the dioxygen sensing hypoxia-inducible factor prolyl hydroxylases has potential therapeutic benefit for treatment of diseases, including anaemia. We describe the discovery of a small-molecule probe useful for monitoring binding to human prolyl hydroxylase domain 2 (PHD2) via fluorescence polarisation. The assay is suitable for high-throughput screening of PHD inhibitors with both weak and strong affinities, as shown by work with clinically used inhibitors and naturally occurring PHD inhibitors.

摘要

抑制双氧传感低氧诱导因子脯氨酰羟化酶对治疗包括贫血在内的疾病具有潜在的治疗益处。我们描述了一种小分子探针的发现,该探针可通过荧光偏振用于监测与人脯氨酰羟化酶结构域 2(PHD2)的结合。该测定法适用于对具有弱和强亲和力的 PHD 抑制剂进行高通量筛选,这一点已通过与临床使用的抑制剂和天然存在的 PHD 抑制剂的工作得到证明。

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