{"title":"基于聚集诱导发射的新型荧光探针选择性识别g -四重体","authors":"Jiahui Zhang, Yu Chen, Yidan Sun, Xinru Li, Haichao Liu, Xiuzhong Wang","doi":"10.1002/bio.70218","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>G-quadruplex (G4) is four-stranded noncanonical secondary DNA structures, which have been identified as potential targets for therapeutic intervention. It is crucial to detect G4 and search for ligands that target G4 with high selectivity in complex biological matrices. The fluorescence signals and circular dichroism spectrum changes were explored for the interaction between jatrorrhizine chloride (Jat), a naturally aggregation-induced emission (AIE) molecule, and various DNA secondary structures. The fluorescence emission intensity was dramatically enhanced after Jat binding to G4 (AA22 as model analyte) compared with other configuration of DNAs, such as single-strand DNA (ssDNA), duplex DNA (dsDNA), hairpin DNA, and i-motif DNA were firstly reported. This means that Jat can serve as a fluorescence probe for the specific recognition of G4 DNA from other DNAs. A label-free AIE-based DNA biosensor to demonstrate the feasibility of detecting DNA polymerase activity and the screening of polymerization-targeted drugs was developed in this paper. The limit of the detection for DNA polymerase activity was 0.007 U·mL<sup>−1</sup>. The results proved that the sensing system has high sensitivity and reproducibility for detection of DNA polymerase activity and can be used for screening DNA polymerase inhibitors based on specific recognition of G4 DNA. In all, it has potential for practical application in chemical and biomedical fields.</p>\n </div>","PeriodicalId":49902,"journal":{"name":"Luminescence","volume":"40 6","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Novel Fluorescent Probe for Selective Recognition of G-Quadruplex Based on Aggregation Induced Emission\",\"authors\":\"Jiahui Zhang, Yu Chen, Yidan Sun, Xinru Li, Haichao Liu, Xiuzhong Wang\",\"doi\":\"10.1002/bio.70218\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>G-quadruplex (G4) is four-stranded noncanonical secondary DNA structures, which have been identified as potential targets for therapeutic intervention. It is crucial to detect G4 and search for ligands that target G4 with high selectivity in complex biological matrices. The fluorescence signals and circular dichroism spectrum changes were explored for the interaction between jatrorrhizine chloride (Jat), a naturally aggregation-induced emission (AIE) molecule, and various DNA secondary structures. The fluorescence emission intensity was dramatically enhanced after Jat binding to G4 (AA22 as model analyte) compared with other configuration of DNAs, such as single-strand DNA (ssDNA), duplex DNA (dsDNA), hairpin DNA, and i-motif DNA were firstly reported. This means that Jat can serve as a fluorescence probe for the specific recognition of G4 DNA from other DNAs. A label-free AIE-based DNA biosensor to demonstrate the feasibility of detecting DNA polymerase activity and the screening of polymerization-targeted drugs was developed in this paper. The limit of the detection for DNA polymerase activity was 0.007 U·mL<sup>−1</sup>. The results proved that the sensing system has high sensitivity and reproducibility for detection of DNA polymerase activity and can be used for screening DNA polymerase inhibitors based on specific recognition of G4 DNA. In all, it has potential for practical application in chemical and biomedical fields.</p>\\n </div>\",\"PeriodicalId\":49902,\"journal\":{\"name\":\"Luminescence\",\"volume\":\"40 6\",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Luminescence\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/bio.70218\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Luminescence","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bio.70218","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
摘要
g -四重体(G4)是四链非规范二级DNA结构,已被确定为治疗干预的潜在靶点。在复杂的生物基质中检测G4并寻找高选择性靶向G4的配体至关重要。研究了天然聚集诱导发射(AIE)分子Jat与多种DNA二级结构相互作用的荧光信号和圆二色光谱变化。与单链DNA (ssDNA)、双链DNA (dsDNA)、发夹DNA和i-motif DNA等其他构型DNA相比,Jat与G4 (AA22为模型分析物)结合后荧光发射强度显著增强。这意味着Jat可以作为荧光探针特异性识别G4 DNA来自其他DNA。本文开发了一种基于ai的无标记DNA生物传感器,以证明检测DNA聚合酶活性和筛选聚合靶向药物的可行性。DNA聚合酶活性的检测限为0.007 U·mL−1。结果表明,该传感系统对DNA聚合酶活性检测具有较高的灵敏度和重复性,可用于基于G4 DNA特异性识别的DNA聚合酶抑制剂筛选。总之,它在化学和生物医学领域具有实际应用的潜力。
Novel Fluorescent Probe for Selective Recognition of G-Quadruplex Based on Aggregation Induced Emission
G-quadruplex (G4) is four-stranded noncanonical secondary DNA structures, which have been identified as potential targets for therapeutic intervention. It is crucial to detect G4 and search for ligands that target G4 with high selectivity in complex biological matrices. The fluorescence signals and circular dichroism spectrum changes were explored for the interaction between jatrorrhizine chloride (Jat), a naturally aggregation-induced emission (AIE) molecule, and various DNA secondary structures. The fluorescence emission intensity was dramatically enhanced after Jat binding to G4 (AA22 as model analyte) compared with other configuration of DNAs, such as single-strand DNA (ssDNA), duplex DNA (dsDNA), hairpin DNA, and i-motif DNA were firstly reported. This means that Jat can serve as a fluorescence probe for the specific recognition of G4 DNA from other DNAs. A label-free AIE-based DNA biosensor to demonstrate the feasibility of detecting DNA polymerase activity and the screening of polymerization-targeted drugs was developed in this paper. The limit of the detection for DNA polymerase activity was 0.007 U·mL−1. The results proved that the sensing system has high sensitivity and reproducibility for detection of DNA polymerase activity and can be used for screening DNA polymerase inhibitors based on specific recognition of G4 DNA. In all, it has potential for practical application in chemical and biomedical fields.
期刊介绍:
Luminescence provides a forum for the publication of original scientific papers, short communications, technical notes and reviews on fundamental and applied aspects of all forms of luminescence, including bioluminescence, chemiluminescence, electrochemiluminescence, sonoluminescence, triboluminescence, fluorescence, time-resolved fluorescence and phosphorescence. Luminescence publishes papers on assays and analytical methods, instrumentation, mechanistic and synthetic studies, basic biology and chemistry.
Luminescence also publishes details of forthcoming meetings, information on new products, and book reviews. A special feature of the Journal is surveys of the recent literature on selected topics in luminescence.