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用于超灵敏检测 microRNA 的单实体电化学生物传感的一对一多对一分析。

One-to-Many Single Entity Electrochemistry Biosensing for Ultrasensitive Detection of microRNA.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences , Wuhan University , Wuhan 430072 , People's Republic of China.

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules and College of Chemistry and Chemical Engineering , Hubei University , Wuhan 430062 , People's Republic of China.

出版信息

Anal Chem. 2020 Jan 7;92(1):853-858. doi: 10.1021/acs.analchem.9b03492. Epub 2019 Dec 9.

Abstract

Single-entity electrochemistry (SEEC), a promising method for biosensing, has an intrinsic limitation on sensitivity since at most one colliding entity can be successfully triggered by one target. Here, we take advantage of one-to-many (1:) signal amplification to develop a new single-entity electrochemistry biosensing (SEECBS), integrating satellite magnetic nanoparticle (MN)-DNA-Pt nanoparticle (NP) conjugates, duplex-specific nuclease (DSN) assisted Pt NPs releasing with stabilization, and effective collision of small sized and nearly naked Pt NPs. Compared with conventional SEECBS, the 1: SEECBS can successfully enrich ∼2 nM Pt NPs by adding 50 aM microRNA (miRNA), in other words, ∼4 × 10 Pt NPs can be triggered by one target. The proposed SEECBS allows the detection of 47 aM miRNA-21, nearly 6 orders of magnitude lower than the previous work, and discrimination of nontarget miRNAs containing even single-nucleotide mismatch. Besides, this method has also been successfully demonstrated for quantification of miRNA in different cell lines. Therefore, the proposed method holds great potential for the application of SEECBS in early diagnosis and prognosis monitoring of cancer.

摘要

单实体电化学(SEEC)作为一种有前途的生物传感方法,由于最多只有一个碰撞实体可以被一个目标成功触发,因此在灵敏度方面存在固有限制。在这里,我们利用一对多(1:)信号放大来开发一种新的单实体电化学生物传感(SEECBS),整合卫星磁性纳米颗粒(MN)-DNA-Pt 纳米颗粒(NP)缀合物、双链特异性核酸酶(DSN)辅助的 Pt NPs 释放与稳定,以及有效碰撞小尺寸和几乎裸露的 Pt NPs。与传统的 SEECBS 相比,1:SEECBS 可以通过添加 50 aM microRNA(miRNA)成功富集约 2 nM Pt NPs,换句话说,一个目标可以触发约 4×10Pt NPs。所提出的 SEECBS 可以检测到 47 aM miRNA-21,比以前的工作低约 6 个数量级,甚至可以区分含有单个核苷酸错配的非靶 miRNA。此外,该方法还成功地用于不同细胞系中 miRNA 的定量。因此,该方法为 SEECBS 在癌症的早期诊断和预后监测中的应用提供了巨大的潜力。

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