Department of Chemistry, Stanford University, Stanford, CA, 94305, USA.
Department of Chemical and Physical Sciences, University of Toronto, Mississauga, ON, L5L 1C6, Canada.
Angew Chem Int Ed Engl. 2018 Sep 24;57(39):12896-12900. doi: 10.1002/anie.201807593. Epub 2018 Sep 3.
The DNA repair enzyme ALKBH2 is implicated in both tumorigenesis as well as resistance to chemotherapy in certain cancers. It is currently under study as a potential diagnostic marker and has been proposed as a therapeutic target. To date, however, there exist no direct methods for measuring the repair activity of ALKBH2 in vitro or in biological samples. Herein, we report a highly specific, fluorogenic probe design based on an oligonucleotide scaffold that reports directly on ALKBH2 activity both in vitro and in cell lysates. Importantly, the probe enables the monitoring of cellular regulation of ALKBH2 activity in response to treatment with the chemotherapy drug temozolomide through a simple fluorescence assay, which has only previously been observed through indirect means such as qPCR and western blots. Furthermore, the probe provides a viable high-throughput assay for drug discovery.
DNA 修复酶 ALKBH2 既与肿瘤发生有关,也与某些癌症的化疗耐药性有关。它目前正在作为一种潜在的诊断标志物进行研究,并被提议作为治疗靶点。然而,目前还没有直接的方法来测量 ALKBH2 在体外或生物样本中的修复活性。在此,我们报告了一种基于寡核苷酸支架的高度特异性荧光探针设计,该设计可直接报告 ALKBH2 在体外和细胞裂解物中的活性。重要的是,该探针通过简单的荧光测定法能够监测化疗药物替莫唑胺处理后细胞对 ALKBH2 活性的调节,而这种监测以前只能通过 qPCR 和 western blot 等间接方法观察到。此外,该探针还为药物发现提供了可行的高通量测定法。