{"title":"用于无标记光敏比色检测microRNA的两端自引诱导级联扩增系统。","authors":"Wenjuan Yi, Yujie Chen, Caiyun Gao, Qiufang Qin and Heping Qin","doi":"10.1039/D5AY00532A","DOIUrl":null,"url":null,"abstract":"<p >MicroRNAs (miRNAs) are pivotal regulators in disease progression and have emerged as significant biomarkers for the early detection, therapeutic intervention, and management of ovarian cancer. The integration of highly sensitive and reliable miRNA detection techniques with ultrasound imaging has the potential to significantly improve the diagnostic accuracy of cancers. In this study, we developed a novel colorimetric approach for the sensitive and reliable detection of miRNAs. This method combines self-priming-mediated DNA polymerization with target recycling and a SYBR Green I (SG)-induced colorimetric response. The sensor operates through a three-stage mechanism: (i) target recognition initiates the formation of a self-priming structure; (ii) an exponential isothermal amplification process, driven by DNA polymerase, facilitates signal amplification; and (iii) a photo-catalyzed color change enables label-free signal generation. Using miRNA-21 as a model target, this approach allows for precise miRNA-21 detection without the need for primers, while the SG-based photo-catalyzed color reaction minimizes background signal interference. The sensor demonstrates the ability to distinguish single-base mismatches in homologous sequences and maintains robust performance in complex biological environments. Furthermore, the sensor has been successfully applied to accurately quantify miRNA-21 levels from constructed samples, highlighting its substantial potential for clinical diagnostics and disease monitoring applications.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":" 24","pages":" 5027-5033"},"PeriodicalIF":2.6000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two-end self-priming induced cascade amplification system for label-free photosensitization colorimetric detection of microRNA†\",\"authors\":\"Wenjuan Yi, Yujie Chen, Caiyun Gao, Qiufang Qin and Heping Qin\",\"doi\":\"10.1039/D5AY00532A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >MicroRNAs (miRNAs) are pivotal regulators in disease progression and have emerged as significant biomarkers for the early detection, therapeutic intervention, and management of ovarian cancer. The integration of highly sensitive and reliable miRNA detection techniques with ultrasound imaging has the potential to significantly improve the diagnostic accuracy of cancers. In this study, we developed a novel colorimetric approach for the sensitive and reliable detection of miRNAs. This method combines self-priming-mediated DNA polymerization with target recycling and a SYBR Green I (SG)-induced colorimetric response. The sensor operates through a three-stage mechanism: (i) target recognition initiates the formation of a self-priming structure; (ii) an exponential isothermal amplification process, driven by DNA polymerase, facilitates signal amplification; and (iii) a photo-catalyzed color change enables label-free signal generation. Using miRNA-21 as a model target, this approach allows for precise miRNA-21 detection without the need for primers, while the SG-based photo-catalyzed color reaction minimizes background signal interference. The sensor demonstrates the ability to distinguish single-base mismatches in homologous sequences and maintains robust performance in complex biological environments. 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引用次数: 0
摘要
MicroRNAs (miRNAs)是疾病进展的关键调节因子,已成为卵巢癌早期检测、治疗干预和管理的重要生物标志物。高灵敏度和可靠的miRNA检测技术与超声成像的结合有可能显著提高癌症的诊断准确性。在这项研究中,我们开发了一种新的比色法来灵敏可靠地检测mirna。该方法结合了自引物介导的DNA聚合和靶循环以及SYBR Green I (SG)诱导的比色响应。传感器通过三阶段机制工作:(i)目标识别启动自启动结构的形成;(ii)由DNA聚合酶驱动的指数等温扩增过程有利于信号扩增;(iii)光催化的颜色变化使无标签信号产生成为可能。使用miRNA-21作为模型靶标,这种方法可以在不需要引物的情况下精确检测miRNA-21,而基于sgg的光催化颜色反应可以最大限度地减少背景信号干扰。该传感器能够区分同源序列中的单碱基错配,并在复杂的生物环境中保持稳健的性能。此外,该传感器已成功应用于准确定量构建样品中的miRNA-21水平,突出了其在临床诊断和疾病监测应用中的巨大潜力。
Two-end self-priming induced cascade amplification system for label-free photosensitization colorimetric detection of microRNA†
MicroRNAs (miRNAs) are pivotal regulators in disease progression and have emerged as significant biomarkers for the early detection, therapeutic intervention, and management of ovarian cancer. The integration of highly sensitive and reliable miRNA detection techniques with ultrasound imaging has the potential to significantly improve the diagnostic accuracy of cancers. In this study, we developed a novel colorimetric approach for the sensitive and reliable detection of miRNAs. This method combines self-priming-mediated DNA polymerization with target recycling and a SYBR Green I (SG)-induced colorimetric response. The sensor operates through a three-stage mechanism: (i) target recognition initiates the formation of a self-priming structure; (ii) an exponential isothermal amplification process, driven by DNA polymerase, facilitates signal amplification; and (iii) a photo-catalyzed color change enables label-free signal generation. Using miRNA-21 as a model target, this approach allows for precise miRNA-21 detection without the need for primers, while the SG-based photo-catalyzed color reaction minimizes background signal interference. The sensor demonstrates the ability to distinguish single-base mismatches in homologous sequences and maintains robust performance in complex biological environments. Furthermore, the sensor has been successfully applied to accurately quantify miRNA-21 levels from constructed samples, highlighting its substantial potential for clinical diagnostics and disease monitoring applications.