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基于聚集诱导发光发光体编码微球的miRNA多重检测

Multiplex detection of miRNAs based on aggregation-induced emission luminogen encoded microspheres.

作者信息

Zou Dan, Wu Weijie, Zhang Jingpu, Ma Qiang, Fan Sisi, Cheng Jin, Li Dan, Niu Jiaqi, Qian Xiaoqing, Li Wanwan, Cui Daxiang

机构信息

Institute of Nano Biomedicine and Engineering, Shanghai Engineering Research Center for Intelligent Instrument for Diagnosis and Therapy, Department of Instrument Science & Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China

National Center for Translational Medicine, Collaborative Innovational Center for System Biology, Shanghai Jiao Tong University Shanghai 200240 P. R. China.

出版信息

RSC Adv. 2019 Dec 4;9(68):39976-39985. doi: 10.1039/c9ra07680h. eCollection 2019 Dec 2.

Abstract

Herein, we report a multiplex detection platform based on a suspension array with aggregation-induced emission luminogen (AIEgen) barcodes for simultaneous quantitative measurement of let-7b-5p, miR-16-5p and miR-19b-3p, which are associated with gastric cancer. A detection strategy by using a flow cytometer is proposed, which utilizes AIEgen-encoded microspheres to quantify the target miRNAs, and phycoerythrin as a fluorescence reporter on the detection probes to provide quantitative signals. This multiplex assay shows good specificity for recognizing single base mismatch, and possesses excellent sensitivity with limits of detection (LODs) ranging from 0.43 to 0.76 nM for the three miRNAs. The approach could be extended to the simultaneous detection of more target miRNAs by designing specific detection probes and increasing the number of fluorescence barcodes. We could foresee it holding great potential in future laboratory research and clinical applications due to its flexibility, strong multiplexed ability and good detection performance.

摘要

在此,我们报告了一种基于悬浮阵列的多重检测平台,该平台带有聚集诱导发光发光体(AIEgen)条形码,用于同时定量测量与胃癌相关的let-7b-5p、miR-16-5p和miR-19b-3p。提出了一种使用流式细胞仪的检测策略,该策略利用AIEgen编码的微球对目标miRNA进行定量,并使用藻红蛋白作为检测探针上的荧光报告分子以提供定量信号。这种多重检测方法在识别单碱基错配方面具有良好的特异性,并且对这三种miRNA具有出色的灵敏度,检测限(LOD)范围为0.43至0.76 nM。通过设计特定的检测探针并增加荧光条形码的数量,该方法可扩展到同时检测更多的目标miRNA。我们可以预见,由于其灵活性、强大的多重检测能力和良好的检测性能,它在未来的实验室研究和临床应用中具有巨大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbb4/9076168/b250be963fdf/c9ra07680h-s1.jpg

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