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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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. |
doi_str_mv | 10.1007/s11426-015-0504-0 |
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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.</description><identifier>ISSN: 1674-7291</identifier><identifier>EISSN: 1869-1870</identifier><identifier>DOI: 10.1007/s11426-015-0504-0</identifier><language>eng</language><publisher>Beijing: Science China Press</publisher><subject>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</subject><ispartof>Science China. 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Chemistry</title><addtitle>Sci. China Chem</addtitle><addtitle>SCIENCE CHINA Chemistry</addtitle><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.</description><subject>Alkaline phosphatase</subject><subject>Biomarkers</subject><subject>Biotin</subject><subject>Chemiluminescence</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Conjugation</subject><subject>Diagnosis</subject><subject>Gene expression</subject><subject>microRNA</subject><subject>MicroRNAs</subject><subject>miRNAs</subject><subject>Phosphatase</subject><subject>Polymerase chain reaction</subject><subject>Target detection</subject><subject>化学发光法</subject><subject>生物标志物</subject><subject>生物素标记</subject><subject>磁珠</subject><subject>超灵敏</subject><subject>逆转录聚合酶链反应</subject><issn>1674-7291</issn><issn>1869-1870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kEtLAzEUhQdRsGh_gLug62gek8csS_EFVUEsLkOSybQpbaadZAr996ZM0Z13kxs43zncUxQ3GN1jhMRDxLgkHCLMIGKohOisGGHJK4ilQOd556KEglT4shjHuEJ5KEVEsFHxPV-nTkcXok9-78Cu1yH5pJNvA2gb8OZt136-TyLYew02ehFc8hYYp-sITQZrYJdu49f9xgeXfRLQMerDdXHR6HV049N7VcyfHr-mL3D28fw6ncygpSVNkDtXG4KsldRKI5gmxFBWC2mJIaI5_nDJLW5qi4RoKsGx4LW20lJDS2boVXE3-G67dte7mNSq7buQI1W-V3IksJRZhQdVPibGzjVq2_mN7g4KI3WsUA0VqlyhOlaoUGbIwMSsDQvX_Tn_B92egpZtWOwy95vEecVLximjP0MSf88</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Zhou, Bingcong</creator><creator>Yang, Haowen</creator><creator>Deng, Yan</creator><creator>Liu, Ming</creator><creator>Liu, Bin</creator><creator>He, Nongyue</creator><creator>Li, Zhiyang</creator><general>Science China Press</general><general>Springer Nature B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>M2P</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20160801</creationdate><title>Ultrasensitive quantitation of MicroRNAs via magnetic beads-based chemiluminesent assay</title><author>Zhou, Bingcong ; Yang, Haowen ; Deng, Yan ; Liu, Ming ; Liu, Bin ; He, Nongyue ; Li, Zhiyang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-6eedb20cc83c8b75a22b35d78c2b27f22b3146c1fdc077f976176dac8c3b345b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Alkaline phosphatase</topic><topic>Biomarkers</topic><topic>Biotin</topic><topic>Chemiluminescence</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Conjugation</topic><topic>Diagnosis</topic><topic>Gene expression</topic><topic>microRNA</topic><topic>MicroRNAs</topic><topic>miRNAs</topic><topic>Phosphatase</topic><topic>Polymerase chain reaction</topic><topic>Target detection</topic><topic>化学发光法</topic><topic>生物标志物</topic><topic>生物素标记</topic><topic>磁珠</topic><topic>超灵敏</topic><topic>逆转录聚合酶链反应</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Bingcong</creatorcontrib><creatorcontrib>Yang, Haowen</creatorcontrib><creatorcontrib>Deng, Yan</creatorcontrib><creatorcontrib>Liu, Ming</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>He, Nongyue</creatorcontrib><creatorcontrib>Li, Zhiyang</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Science China. Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Bingcong</au><au>Yang, Haowen</au><au>Deng, Yan</au><au>Liu, Ming</au><au>Liu, Bin</au><au>He, Nongyue</au><au>Li, Zhiyang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrasensitive quantitation of MicroRNAs via magnetic beads-based chemiluminesent assay</atitle><jtitle>Science China. Chemistry</jtitle><stitle>Sci. China Chem</stitle><addtitle>SCIENCE CHINA Chemistry</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>59</volume><issue>8</issue><spage>1051</spage><epage>1058</epage><pages>1051-1058</pages><issn>1674-7291</issn><eissn>1869-1870</eissn><abstract>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.</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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