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基于单个等离子体微珠的无扩增和混合读取分析多重 microRNAs。

Amplification-Free and Mix-and-Read Analysis of Multiplexed MicroRNAs on a Single Plasmonic Microbead.

机构信息

Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Xi'an, Shaanxi Province 710119, P. R. China.

Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, Xi'an, Shaanxi Province 710119, P. R. China.

出版信息

Nano Lett. 2021 Aug 11;21(15):6718-6724. doi: 10.1021/acs.nanolett.1c02473. Epub 2021 Jul 29.

DOI:10.1021/acs.nanolett.1c02473
PMID:34324345
Abstract

In this work, a single microbead covered with a plasmonic layer is employed as the microreactor for the multiplexed miRNA analysis without nucleic acid amplification. On the plasmonic layer, the S9.6 antibody is adopted as the universal module for binding DNA/miRNA duplexes regardless of the sequence. Meanwhile, there is also a SERS reporter gold nanoparticle (GNP) pool, in which each group of GNPs is labeled with both a Raman coding molecule and a DNA probe for recognizing a given miRNA of interest. The target miRNAs will lead to the specific capture of the corresponding SERS reporter GNPs onto the plasmonic layer, which will enormously enhance the target miRNA-induced SERS signals. Finally, the enhanced SERS signals concentrated on the microbead will be mapped out by a confocal Raman microscope. The proposed method achieves the high-precision sensing of sub-pM target miRNA in a simple mix-and-read format and possesses multiplexed assay capability.

摘要

在这项工作中,采用单个覆盖有等离子体层的微珠作为微反应器,无需核酸扩增即可对多重 miRNA 进行分析。在等离子体层上,采用 S9.6 抗体作为通用模块,用于结合 DNA/miRNA 双链,而与序列无关。同时,还有一个 SERS 报告金纳米粒子(GNP)池,其中每组 GNP 都标记有拉曼编码分子和用于识别特定感兴趣 miRNA 的 DNA 探针。靶 miRNA 将导致相应的 SERS 报告 GNP 特异性捕获到等离子体层上,这将极大地增强靶 miRNA 诱导的 SERS 信号。最后,通过共焦 Raman 显微镜对集中在微珠上的增强 SERS 信号进行映射。该方法以简单的混合读取格式实现了对亚皮摩尔靶 miRNA 的高精度传感,并具有多重分析能力。

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