Jing Jiang, Guohai Lin, Hengxin Yu, Liqun Chen, Huo Xu
{"title":"用于高保真microRNA成像和临床液体活检的自组装DNA纳米球驱动的无约束自循环放大器。","authors":"Jing Jiang, Guohai Lin, Hengxin Yu, Liqun Chen, Huo Xu","doi":"10.1016/j.talanta.2026.130416","DOIUrl":null,"url":null,"abstract":"<p><p>The development of predictable and thermodynamically stable DNA nanomachines remains challenging for the monitoring of intracellular microRNAs (miRNAs) in complex biological matrices. In this study, a fluorescent biosensor utilizing a confined-free synergistic configuration is presented for the precise detection of miR-21. To mitigate the thermodynamic limitations of homogeneous catalytic hairpin assembly (CHA), a process in which unconstrained molecular diffusion induces background leakage, the amplification components were spatially partitioned. The sensing platform incorporates a rigid DNA nanosphere (NP), assembled via the annealing of three palindromic sequences, which serves as a sterically hindered scaffold to strictly confine hairpin probe 1 (HP1). Target miR-21 initiates the opening of the anchored HP1, subsequently recruiting freely diffusible auxiliary probes (HP2 and HP3) to form a localized Y-shaped complex. This reaction generates a surrogate miR-21 sequence that detaches and unlocks adjacent HP1 probes, establishing an inter-particle chemical communication network. By integrating nanoscale spatial confinement with this propagated catalytic cascade, the proposed confined-free self-circulating amplifier (CF-SCA) suppresses background leakage while maintaining rapid mass transfer, yielding a limit of detection of 100 pM. Additionally, the dense 3D nanoscaffold provides nuclease resistance. Following liposome-mediated cellular delivery, the confined-free mechanism counteracts macromolecular crowding, facilitating in situ dynamic imaging of miR-21 in living cancer cells. Evaluated through the stratification of clinical serum samples from multiple cancer cohorts, the CF-SCA nanoplatform offers an enzyme-free tool for clinical diagnostics and liquid biopsy applications.</p>","PeriodicalId":435,"journal":{"name":"Talanta","volume":"312 Pt A","pages":"130416"},"PeriodicalIF":6.7000,"publicationDate":"2027-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-assembled DNA nanosphere-powered confined-free self-circulating amplifier for high-fidelity microRNA imaging and clinical liquid biopsy.\",\"authors\":\"Jing Jiang, Guohai Lin, Hengxin Yu, Liqun Chen, Huo Xu\",\"doi\":\"10.1016/j.talanta.2026.130416\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The development of predictable and thermodynamically stable DNA nanomachines remains challenging for the monitoring of intracellular microRNAs (miRNAs) in complex biological matrices. In this study, a fluorescent biosensor utilizing a confined-free synergistic configuration is presented for the precise detection of miR-21. To mitigate the thermodynamic limitations of homogeneous catalytic hairpin assembly (CHA), a process in which unconstrained molecular diffusion induces background leakage, the amplification components were spatially partitioned. The sensing platform incorporates a rigid DNA nanosphere (NP), assembled via the annealing of three palindromic sequences, which serves as a sterically hindered scaffold to strictly confine hairpin probe 1 (HP1). Target miR-21 initiates the opening of the anchored HP1, subsequently recruiting freely diffusible auxiliary probes (HP2 and HP3) to form a localized Y-shaped complex. This reaction generates a surrogate miR-21 sequence that detaches and unlocks adjacent HP1 probes, establishing an inter-particle chemical communication network. By integrating nanoscale spatial confinement with this propagated catalytic cascade, the proposed confined-free self-circulating amplifier (CF-SCA) suppresses background leakage while maintaining rapid mass transfer, yielding a limit of detection of 100 pM. Additionally, the dense 3D nanoscaffold provides nuclease resistance. Following liposome-mediated cellular delivery, the confined-free mechanism counteracts macromolecular crowding, facilitating in situ dynamic imaging of miR-21 in living cancer cells. Evaluated through the stratification of clinical serum samples from multiple cancer cohorts, the CF-SCA nanoplatform offers an enzyme-free tool for clinical diagnostics and liquid biopsy applications.</p>\",\"PeriodicalId\":435,\"journal\":{\"name\":\"Talanta\",\"volume\":\"312 Pt A\",\"pages\":\"130416\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2027-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Talanta\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1016/j.talanta.2026.130416\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/8/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Talanta","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.talanta.2026.130416","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Self-assembled DNA nanosphere-powered confined-free self-circulating amplifier for high-fidelity microRNA imaging and clinical liquid biopsy.
The development of predictable and thermodynamically stable DNA nanomachines remains challenging for the monitoring of intracellular microRNAs (miRNAs) in complex biological matrices. In this study, a fluorescent biosensor utilizing a confined-free synergistic configuration is presented for the precise detection of miR-21. To mitigate the thermodynamic limitations of homogeneous catalytic hairpin assembly (CHA), a process in which unconstrained molecular diffusion induces background leakage, the amplification components were spatially partitioned. The sensing platform incorporates a rigid DNA nanosphere (NP), assembled via the annealing of three palindromic sequences, which serves as a sterically hindered scaffold to strictly confine hairpin probe 1 (HP1). Target miR-21 initiates the opening of the anchored HP1, subsequently recruiting freely diffusible auxiliary probes (HP2 and HP3) to form a localized Y-shaped complex. This reaction generates a surrogate miR-21 sequence that detaches and unlocks adjacent HP1 probes, establishing an inter-particle chemical communication network. By integrating nanoscale spatial confinement with this propagated catalytic cascade, the proposed confined-free self-circulating amplifier (CF-SCA) suppresses background leakage while maintaining rapid mass transfer, yielding a limit of detection of 100 pM. Additionally, the dense 3D nanoscaffold provides nuclease resistance. Following liposome-mediated cellular delivery, the confined-free mechanism counteracts macromolecular crowding, facilitating in situ dynamic imaging of miR-21 in living cancer cells. Evaluated through the stratification of clinical serum samples from multiple cancer cohorts, the CF-SCA nanoplatform offers an enzyme-free tool for clinical diagnostics and liquid biopsy applications.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.