Institute for Molecules and Materials, Radboud University Nijmegen, Heyendaalseweg 135, 6525 AJ, Nijmegen, The Netherlands.
Angew Chem Int Ed Engl. 2023 Apr 24;62(18):e202302796. doi: 10.1002/anie.202302796. Epub 2023 Mar 27.
Terminal deoxynucleotidyl Transferase (TdT) is a template-independent DNA polymerase that plays an essential role in the human adaptive immune system and is upregulated in several types of leukemia. It has therefore gained interest as a leukemia biomarker and potential therapeutic target. Herein, we describe a FRET-quenched fluorogenic probe based on a size-expanded deoxyadenosine that reports directly on TdT enzymatic activity. The probe enables real-time detection of primer extension and de novo synthesis activity of TdT and displays selectivity over other polymerase and phosphatase enzymes. Importantly, TdT activity and its response to treatment with a promiscuous polymerase inhibitor could be monitored in human T-lymphocyte cell extract and Jurkat cells using a simple fluorescence assay. Finally, employing the probe in a high-throughput assay resulted in the identification of a non-nucleoside TdT inhibitor.
末端脱氧核苷酸转移酶(TdT)是一种无模板依赖的 DNA 聚合酶,在人类适应性免疫系统中发挥着重要作用,并且在几种类型的白血病中上调。因此,它作为白血病生物标志物和潜在的治疗靶点引起了人们的兴趣。本文描述了一种基于脱氧腺苷的扩展大小的荧光共振能量转移(FRET)猝灭荧光探针,该探针可直接报告 TdT 酶活性。该探针能够实时检测 TdT 的引物延伸和从头合成活性,并对其他聚合酶和磷酸酶具有选择性。重要的是,使用简单的荧光测定法,可以在人 T 淋巴细胞提取物和 Jurkat 细胞中监测 TdT 活性及其对杂乱无章的聚合酶抑制剂的反应。最后,在高通量测定中使用该探针,鉴定出一种非核苷 TdT 抑制剂。