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通过锚定嵌入DNA探针特异性监测DNA解旋酶功能

Specific Monitoring the DNA Helicase Function via Anchor-Embedded DNA Probe.

作者信息

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

机构信息

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.

出版信息

Adv Sci (Weinh). 2025 Feb;12(8):e2413368. doi: 10.1002/advs.202413368. Epub 2024 Dec 31.

DOI:10.1002/advs.202413368
PMID:39737862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11848566/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/8c6fb81b2cf7/ADVS-12-2413368-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/464882df8032/ADVS-12-2413368-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/d5bcd91bf9ae/ADVS-12-2413368-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/3639fb07050e/ADVS-12-2413368-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/d5d7a5efd506/ADVS-12-2413368-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/ae873fa4b9b0/ADVS-12-2413368-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/bce95ccde5d0/ADVS-12-2413368-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/52ca328d05ad/ADVS-12-2413368-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/8c6fb81b2cf7/ADVS-12-2413368-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/464882df8032/ADVS-12-2413368-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/d5bcd91bf9ae/ADVS-12-2413368-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/3639fb07050e/ADVS-12-2413368-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/d5d7a5efd506/ADVS-12-2413368-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/ae873fa4b9b0/ADVS-12-2413368-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/bce95ccde5d0/ADVS-12-2413368-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/52ca328d05ad/ADVS-12-2413368-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11848566/8c6fb81b2cf7/ADVS-12-2413368-g009.jpg

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本文引用的文献

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Bacteriophage λ exonuclease and a 5'-phosphorylated DNA guide allow PAM-independent targeting of double-stranded nucleic acids.噬菌体λ核酸外切酶和5'-磷酸化DNA向导可实现对双链核酸的PAM非依赖性靶向。
Nat Biotechnol. 2024 Sep 18. doi: 10.1038/s41587-024-02388-9.
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Discovery of WRN inhibitor HRO761 with synthetic lethality in MSI cancers.WRN 抑制剂 HRO761 在 MSI 癌症中具有合成致死性。
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Chemoproteomic discovery of a covalent allosteric inhibitor of WRN helicase.
WRN 解旋酶共价变构抑制剂的化学生物学发现。
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Targeting ATP-binding site of WRN Helicase: Identification of novel inhibitors through pocket analysis and Molecular Dynamics-Enhanced virtual screening.靶向 WRN 解旋酶的 ATP 结合位点:通过口袋分析和分子动力学增强虚拟筛选鉴定新型抑制剂。
Bioorg Med Chem Lett. 2024 May 15;104:129711. doi: 10.1016/j.bmcl.2024.129711. Epub 2024 Mar 21.
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Challenges for the Discovery of Non-Covalent WRN Helicase Inhibitors.WRN 解旋酶非共价抑制剂发现面临的挑战。
ChemMedChem. 2024 Apr 16;19(8):e202300613. doi: 10.1002/cmdc.202300613. Epub 2024 Mar 7.
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Coarse-grained model simulation-guided localized DNA signal amplification probe for miRNA detection.用于miRNA检测的粗粒度模型模拟引导的局部DNA信号放大探针
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Chimeric d/l-DNA Probes of Base Excision Repair Enable Real-Time Monitoring of Thymine DNA Glycosylase Activity in Live Cells.嵌合 d/l-DNA 探针的碱基切除修复使实时监测胸腺嘧啶 DNA 糖基化酶活性在活细胞中。
J Am Chem Soc. 2023 Aug 9;145(31):17066-17074. doi: 10.1021/jacs.3c03010. Epub 2023 Jul 26.
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A review for cell-based screening methods in drug discovery.药物发现中基于细胞的筛选方法综述。
Biophys Rep. 2021 Dec 31;7(6):504-516. doi: 10.52601/bpr.2021.210042.
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