Acero Rosemarie Elloisa P, Deckard Charles E, Sczepanski Jonathan T
Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843, United States.
ACS Sens. 2025 Aug 22;10(8):5655-5663. doi: 10.1021/acssensors.5c00730. Epub 2025 Aug 4.
Base excision repair (BER) is a biologically and biomedically important cellular pathway responsible for repairing common DNA lesions. As a central member of the BER pathway, apurinic/apyrimidinic endonuclease 1 (APE1) is important in DNA repair and has been identified as a diagnostic and predictive biomarker for several diseases, motivating the development of analytical methods. However, the current repertoire of APE1 probes, the majority of which are derived from nucleic acids, are poorly suited for use in living cells and organisms, putting many promising biomedical applications of APE1 out of reach. Here, we exploit the bio-orthogonal properties of mirror-image l-DNA, together with a novel chimeric d/l-DNA molecular beacon architecture, to develop a highly versatile probe for intracellular BER, which we apply to the detection of APE1. The chimeric probe is simple to use, biostable, fast, and permits both real-time and light-controlled monitoring of APE1 activity in the nucleus of living cells, making it well suited for diverse intracellular applications. For example, we show that the probe can rapidly distinguish cells based on different APE1 expression levels and can monitor dynamic APE1 activity at single-cell resolution. Moreover, the generality of the probe design allowed for the development of a multiplexed assay for simultaneous imaging of APE1 and DNA glycosylase activities in living cells, which we used to reveal new insights into the efficacy of several prominent APE1 inhibitors. Overall, the chimeric d/l-DNA beacon probe presented in this work will be highly useful for researchers studying BER and provides a versatile toolkit for the development of improved BER-targeted therapies.
碱基切除修复(BER)是一种在生物学和生物医学上都很重要的细胞途径,负责修复常见的DNA损伤。作为BER途径的核心成员,脱嘌呤/脱嘧啶内切酶1(APE1)在DNA修复中很重要,并且已被确定为几种疾病的诊断和预测生物标志物,这推动了分析方法的发展。然而,目前的APE1探针库,其中大多数来自核酸,不太适合在活细胞和生物体中使用,使得APE1的许多有前景的生物医学应用无法实现。在这里,我们利用镜像l-DNA的生物正交特性,结合一种新型的嵌合d/l-DNA分子信标结构,开发了一种用于细胞内BER的高度通用的探针,并将其应用于APE1的检测。这种嵌合探针使用简单、生物稳定、快速,能够对活细胞核中的APE1活性进行实时和光控监测,非常适合多种细胞内应用。例如,我们表明该探针可以根据不同的APE1表达水平快速区分细胞,并能够在单细胞分辨率下监测动态的APE1活性。此外,探针设计的通用性使得能够开发一种多重检测方法,用于同时成像活细胞中的APE1和DNA糖基化酶活性,我们用它来揭示几种著名的APE1抑制剂疗效的新见解。总体而言,本文介绍的嵌合d/l-DNA信标探针将对研究BER的研究人员非常有用,并为开发改进的靶向BER的疗法提供了一个通用的工具包。