Ultrasensitive quantitation of MicroRNAs via magnetic beads-based chemiluminesent assay

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level, and their aberrant expression occurs during the development of malignant diseases. Recently, miRNAs have been proposed as potential prognostic and predictive biomarkers for early diagnosis....

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Veröffentlicht in:Science China. Chemistry 2016-08, Vol.59 (8), p.1051-1058
Hauptverfasser: Zhou, Bingcong, Yang, Haowen, Deng, Yan, Liu, Ming, Liu, Bin, He, Nongyue, Li, Zhiyang
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container_issue 8
container_start_page 1051
container_title Science China. Chemistry
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creator Zhou, Bingcong
Yang, Haowen
Deng, Yan
Liu, Ming
Liu, Bin
He, Nongyue
Li, Zhiyang
description MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level, and their aberrant expression occurs during the development of malignant diseases. Recently, miRNAs have been proposed as potential prognostic and predictive biomarkers for early diagnosis. However, a major obstacle in rapid miRNA analysis from real samples is the lack of ultrasensitive and quantitative techniques. In this regard, the use of chemiluminescence (CL) system offers a highly sensitive strategy for detecting miRNAs. In this article, an ultrasensitive approach has been established for the quantification ofmiRNAs, using magnetic beads (MBs) and alkaline phosphatase (AP)-based CL system. This technique depends on sandwich hybridization among MBs-labeled capture probes, target miRNAs and biotin-labeled reporter probes, conjugation of streptavidin-alkaline phosphatase (SA-AP) to biotin-labeled reporter probes, and CL detection of AP-linked targets. Detection of miR-21 with this technique demonstrated a high selectivity and an ultralow limit of detection (LOD) of 60 fM with an extraordinarily wide range of six orders of magnitudes. The quantitation could be achieved by direct detecting target miRNA in serum samples within a total time of 1.5 h and did not require reverse transcription and polymerase chain reaction (PCR) amplification. Therefore, this developed method shows great potential for early cancer diagnosis based on miRNAs as biomarkers.
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Recently, miRNAs have been proposed as potential prognostic and predictive biomarkers for early diagnosis. However, a major obstacle in rapid miRNA analysis from real samples is the lack of ultrasensitive and quantitative techniques. In this regard, the use of chemiluminescence (CL) system offers a highly sensitive strategy for detecting miRNAs. In this article, an ultrasensitive approach has been established for the quantification ofmiRNAs, using magnetic beads (MBs) and alkaline phosphatase (AP)-based CL system. This technique depends on sandwich hybridization among MBs-labeled capture probes, target miRNAs and biotin-labeled reporter probes, conjugation of streptavidin-alkaline phosphatase (SA-AP) to biotin-labeled reporter probes, and CL detection of AP-linked targets. Detection of miR-21 with this technique demonstrated a high selectivity and an ultralow limit of detection (LOD) of 60 fM with an extraordinarily wide range of six orders of magnitudes. The quantitation could be achieved by direct detecting target miRNA in serum samples within a total time of 1.5 h and did not require reverse transcription and polymerase chain reaction (PCR) amplification. Therefore, this developed method shows great potential for early cancer diagnosis based on miRNAs as biomarkers.</abstract><cop>Beijing</cop><pub>Science China Press</pub><doi>10.1007/s11426-015-0504-0</doi><tpages>8</tpages></addata></record>
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subjects Alkaline phosphatase
Biomarkers
Biotin
Chemiluminescence
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Conjugation
Diagnosis
Gene expression
microRNA
MicroRNAs
miRNAs
Phosphatase
Polymerase chain reaction
Target detection
化学发光法
生物标志物
生物素标记
磁珠
超灵敏
逆转录聚合酶链反应
title Ultrasensitive quantitation of MicroRNAs via magnetic beads-based chemiluminesent assay
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