Ning Keni, Tang Xiaoyan, Li Zhe, Zhong Liting, Zhou Yingchen, Wang Jiaen, Huang Wanyi, Zhang Han, Ke Jiajun, Luan Tiangang, Chen Shuo-Bin, Zhai Junqiu
School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
School of Pharmaceutical Sciences, Guangdong Provincial Key Laboratory of New Drug Design and Evaluation, Sun Yat-Sen University, Guangzhou, 510006, China.
Adv Sci (Weinh). 2025 Feb;12(8):e2413368. doi: 10.1002/advs.202413368. Epub 2024 Dec 31.
DNA helicases play a pivotal role in maintaining genome integrity by unwinding the DNA double helix and are often considered promising targets for drug development. However, assessing specific DNA helicase activity in living cells remains challenging. Herein, the first anchor-embedded duplex (ATED) probe, 17GC, is constructed to uniquely monitor the unwinding activity of Werner syndrome helicase (WRN), a clinical anticancer target. This probe integrates biophysical screening and molecular simulation approaches. The 17GC probe consists of two components: the first one is a bubble structure as an anchor for recruiting WRN in cells, and the second one is GC-rich double helices on both ends of the bubble, which allow high sensitivity in detecting WRN activity. In vitro evaluations demonstrate that 17GC is highly sensitive and specific to WRN (LOD = 33.5 pm) compared to a wide range of other enzymes, including helicases and nucleases. Cellular evaluation reveals that the ATED probe exhibits remarkable performance in monitoring WRN helicase activity and assessing the inhibitory efficiency of clinical WRN inhibitors in various cell types. This study introduces a novel approach for designing specific and sensitive probes for DNA helicases in cells, which holds promise for biological characterization and drug development.
DNA解旋酶通过解开DNA双螺旋在维持基因组完整性方面发挥着关键作用,并且常常被认为是药物开发的有前景的靶点。然而,在活细胞中评估特定DNA解旋酶的活性仍然具有挑战性。在此,构建了首个锚定嵌入双链体(ATED)探针17GC,以独特地监测作为临床抗癌靶点的沃纳综合征解旋酶(WRN)的解旋活性。该探针整合了生物物理筛选和分子模拟方法。17GC探针由两个部分组成:第一个是作为在细胞中招募WRN的锚的气泡结构,第二个是气泡两端富含GC的双螺旋,这使得在检测WRN活性时具有高灵敏度。体外评估表明,与包括解旋酶和核酸酶在内的多种其他酶相比,17GC对WRN具有高度敏感性和特异性(检测限 = 33.5皮摩尔)。细胞评估显示,ATED探针在监测WRN解旋酶活性和评估临床WRN抑制剂在各种细胞类型中的抑制效率方面表现出色。本研究介绍了一种为细胞中的DNA解旋酶设计特异性和灵敏性探针的新方法,这为生物学表征和药物开发带来了希望。