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利用链置换引发滚环扩增和荧光共振能量转移检测 microRNAs。

Detection of microRNAs using toehold-initiated rolling circle amplification and fluorescence resonance energy transfer.

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Institute of Biomedical Sciences, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan, 250014, PR China.

Medical Research Center, Shandong Provincial Qianfoshan Hospital, the First Hospital affiliated with Shandong First Medical University, Jinan, 250014, PR China.

出版信息

Talanta. 2020 Jan 15;207:120285. doi: 10.1016/j.talanta.2019.120285. Epub 2019 Aug 24.

Abstract

Detection of microRNAs (miRNAs) in cells improves our understanding of their physiological functions and facilitates exploration of their roles diseases. The toehold-mediated strand displacement reaction initiates rolling circle amplification (RCA) to achieve signal amplification of the specific miRNA; This process is named as toehold-initiated RCA (TIRCA). The product of TIRCA was ligated to two DNA probes, which were modified with 6-carboxyfluorescein and carboxytetramethylrhodamine, respectively. Qualitative detection of miRNAs was successfully achieved by combining the fluorescence aggregation enhancement effect with fluorescence resonance energy transfer generated by the proximity of the two fluorescent dyes. Thus, this approach helps us analyze the roles of miRNAs in human disease more accurately.

摘要

细胞中 microRNAs(miRNAs)的检测有助于我们理解其生理功能,并深入探究它们在疾病中的作用。通过引发滚环扩增(RCA)的链置换反应实现对特定 miRNA 的信号放大;这一过程被命名为引发滚环扩增(TIRCA)。TIRCA 的产物连接到两个 DNA 探针上,这两个探针分别用 6-羧基荧光素和羧基四甲基罗丹明修饰。通过结合两种荧光染料的临近产生的荧光聚集增强效应和荧光共振能量转移,成功实现了 miRNA 的定性检测。因此,这种方法有助于我们更准确地分析 miRNA 在人类疾病中的作用。

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