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利用阳离子共轭聚合物材料进行多重 microRNAs 的可视化检测。

Visual Detection of Multiplex MicroRNAs Using Cationic Conjugated Polymer Materials.

机构信息

Key Laboratory of Medicinal Chemistry and Molecular Diagnosis, Ministry of Education, Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Environmental Science, Hebei University , Baoding 071002, Hebei, P. R. China.

Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2016 Jan 20;8(2):1520-6. doi: 10.1021/acsami.5b11135. Epub 2016 Jan 6.

Abstract

A simple, visual, and specific method for simultaneous detection of multiplex microRNAs (miRNAs) has been developed by integrating duplex-specific nuclease (DSN)-induced amplification with cationic conjugated polymer (CCP) materials. The probe DNA with a complementary sequence to target miRNA is labeled with fluorescein dye (FAM). Without target miRNA, the single-strand DNA probe cannot be digested by DSN. Upon adding CCPs, efficient fluorescence resonance energy transfer (FRET) from CCP to FAM occurs owing to strong electrostatic interactions between CCP and the DNA probe. In the presence of target miRNA, the DNA probe hybridizes with target miRNA followed by digestion to small nucleotide fragments by DSN; meanwhile, the miRNA is released and subsequently interacts again with the probe, resulting in the cycled digestion of the DNA probe. In this case, weak electrostatic interactions between oligonucleotide fragments and CCP lead to inefficient FRET from CCP to FAM. Thus, by triggering the FRET signal from CCP to FAM, miRNA can be specially detected, and the fluorescence color change based on FRET can be visualized directly with the naked eye under an UV lamp. Furthermore, an energy transfer cascade can be designed using CCP and DNA probes labeled at the 5'-terminus with FAM and Cy3 dyes, and the multistep FRET processes offer the ability of simultaneous detection of multiplex miRNAs.

摘要

一种简单、直观、特异的多重 microRNA(miRNA)同时检测方法,是通过将双链特异性核酸酶(DSN)诱导的扩增与阳离子共轭聚合物(CCP)材料相结合而开发的。与靶 miRNA 互补的探针 DNA 用荧光素染料(FAM)标记。没有靶 miRNA 时,DSN 无法消化单链 DNA 探针。加入 CCP 后,由于 CCP 与 DNA 探针之间的强静电相互作用,会发生有效的荧光共振能量转移(FRET)从 CCP 到 FAM。在存在靶 miRNA 的情况下,DNA 探针与靶 miRNA 杂交,随后被 DSN 切割成小核苷酸片段;同时,miRNA 被释放并再次与探针相互作用,导致 DNA 探针的循环消化。在这种情况下,寡核苷酸片段与 CCP 之间的弱静电相互作用导致从 CCP 到 FAM 的 FRET 效率降低。因此,通过触发从 CCP 到 FAM 的 FRET 信号,可以特异性检测 miRNA,并且可以在 UV 灯下直接用肉眼观察基于 FRET 的荧光颜色变化。此外,可以使用 CCP 和在 5'-末端用 FAM 和 Cy3 染料标记的 DNA 探针设计能量转移级联,并且多步 FRET 过程提供了同时检测多重 miRNA 的能力。

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