Simultaneous detection of multiple mutations in epidermal growth factor receptor based on fluorescence quenching of quantum dots

► We develop a simultaneous detection method for multiple mutations. ► We detect two common mutations in the epidermal growth factor receptor gene. ► Fluorescence quenching due to aggregation of quantum dots is used for detection. ► This enables a simultaneous detection of mutations in exon 19 and 2...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biosensors & bioelectronics 2012-01, Vol.31 (1), p.558-561
Hauptverfasser: Kang, Taegyeong, Lee, Hosub, Choe, Dongcheol, Joo, Sang-Woo, Lee, So Yeong, Yoon, Kyong-Ah, Lee, Kangtaek
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 561
container_issue 1
container_start_page 558
container_title Biosensors & bioelectronics
container_volume 31
creator Kang, Taegyeong
Lee, Hosub
Choe, Dongcheol
Joo, Sang-Woo
Lee, So Yeong
Yoon, Kyong-Ah
Lee, Kangtaek
description ► We develop a simultaneous detection method for multiple mutations. ► We detect two common mutations in the epidermal growth factor receptor gene. ► Fluorescence quenching due to aggregation of quantum dots is used for detection. ► This enables a simultaneous detection of mutations in exon 19 and 21 of EGFR gene. We have developed a simultaneous detection method for two common mutations in the epidermal growth factor receptor gene based on the fluorescence quenching phenomenon caused by aggregation of CdSe quantum dots. For detection of the in-frame deletion in exon 19 and the L858R point mutation in exon 21, water-soluble CdSe quantum dots with two sizes were functionalized using four different types of probe oligonucleotides. Addition of target oligonucleotides with the deletion mutation in exon 19 into the suspensions caused crosslinking-induced aggregation of green-emitting quantum dots, followed by the fluorescence quenching while that with the L858R point mutation resulted in aggregation of yellow-emitting quantum dots. In addition, targets with both deletion and point mutations caused aggregation of both green- and yellow-emitting quantum dots. This method allows a simultaneous detection of mutations in exon 19 and 21 of EGFR gene in a single experiment. We found that minimum mutant concentration that could be detected by this method was as low as 2% for deletion mutation, and 5% for point mutation. PCR products of EGFR gene were also used to confirm that our method could be used to detect mutation in amplified DNA fragments.
doi_str_mv 10.1016/j.bios.2011.10.025
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_920803583</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0956566311006932</els_id><sourcerecordid>920803583</sourcerecordid><originalsourceid>FETCH-LOGICAL-c417t-fc171364baa1662fbaf92185b01d1aa474d7e3cf3f7dfa2f429e89b33e002fa53</originalsourceid><addsrcrecordid>eNqFkUtv1TAQhS1ERS-FP8ACeYO6yq1fiROJDarKQ6rEAlhbjj1ufZXEqe1QseOnY-teYAerGR19czQzB6FXlOwpod3VYT_6kPaMUFqEPWHtE7SjveSNYLx9inZkaLum7Tp-jp6ndCCESDqQZ-icMSL7Xogd-vnFz9uU9QJhS9hCBpN9WHBwuOp-naA0WVcxYb9gWL2FOOsJ38XwmO-x0yaHiCMYWGsz6gQWFws3bSFCMrAYwA9bKfd-uavOD5te8jZjG3J6gc6cnhK8PNUL9O39zdfrj83t5w-frt_dNkZQmRtnqKS8E6PWtOuYG7UbGO3bkVBLtRZSWAncOO6kdZo5wQboh5FzIIQ53fILdHn0XWMoy6SsZl92m6bj6WpgpCe87fn_Sco5bQWThWRH0sSQUgSn1uhnHX8oSlSNSB1UjUjViKpWIipDr0_22ziD_TPyO5MCvDkBOhk9uagX49NfrqMFZKxwb48clLd99xBVMr4-2_oSRlY2-H_t8QundbKJ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>913315427</pqid></control><display><type>article</type><title>Simultaneous detection of multiple mutations in epidermal growth factor receptor based on fluorescence quenching of quantum dots</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Kang, Taegyeong ; Lee, Hosub ; Choe, Dongcheol ; Joo, Sang-Woo ; Lee, So Yeong ; Yoon, Kyong-Ah ; Lee, Kangtaek</creator><creatorcontrib>Kang, Taegyeong ; Lee, Hosub ; Choe, Dongcheol ; Joo, Sang-Woo ; Lee, So Yeong ; Yoon, Kyong-Ah ; Lee, Kangtaek</creatorcontrib><description>► We develop a simultaneous detection method for multiple mutations. ► We detect two common mutations in the epidermal growth factor receptor gene. ► Fluorescence quenching due to aggregation of quantum dots is used for detection. ► This enables a simultaneous detection of mutations in exon 19 and 21 of EGFR gene. We have developed a simultaneous detection method for two common mutations in the epidermal growth factor receptor gene based on the fluorescence quenching phenomenon caused by aggregation of CdSe quantum dots. For detection of the in-frame deletion in exon 19 and the L858R point mutation in exon 21, water-soluble CdSe quantum dots with two sizes were functionalized using four different types of probe oligonucleotides. Addition of target oligonucleotides with the deletion mutation in exon 19 into the suspensions caused crosslinking-induced aggregation of green-emitting quantum dots, followed by the fluorescence quenching while that with the L858R point mutation resulted in aggregation of yellow-emitting quantum dots. In addition, targets with both deletion and point mutations caused aggregation of both green- and yellow-emitting quantum dots. This method allows a simultaneous detection of mutations in exon 19 and 21 of EGFR gene in a single experiment. We found that minimum mutant concentration that could be detected by this method was as low as 2% for deletion mutation, and 5% for point mutation. PCR products of EGFR gene were also used to confirm that our method could be used to detect mutation in amplified DNA fragments.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2011.10.025</identifier><identifier>PMID: 22078844</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Biological and medical sciences ; Biotechnology ; DNA Mutational Analysis - instrumentation ; DNA Probes - genetics ; Epidermal growth factor receptor ; Equipment Design ; Equipment Failure Analysis ; Fluorescence ; Fundamental and applied biological sciences. Psychology ; Mutation ; Oligonucleotide Array Sequence Analysis - instrumentation ; Quantum Dots ; Quenching ; Receptor, Epidermal Growth Factor - genetics ; Reproducibility of Results ; Sensitivity and Specificity ; Spectrometry, Fluorescence - instrumentation</subject><ispartof>Biosensors &amp; bioelectronics, 2012-01, Vol.31 (1), p.558-561</ispartof><rights>2011 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-fc171364baa1662fbaf92185b01d1aa474d7e3cf3f7dfa2f429e89b33e002fa53</citedby><cites>FETCH-LOGICAL-c417t-fc171364baa1662fbaf92185b01d1aa474d7e3cf3f7dfa2f429e89b33e002fa53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bios.2011.10.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26107822$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22078844$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kang, Taegyeong</creatorcontrib><creatorcontrib>Lee, Hosub</creatorcontrib><creatorcontrib>Choe, Dongcheol</creatorcontrib><creatorcontrib>Joo, Sang-Woo</creatorcontrib><creatorcontrib>Lee, So Yeong</creatorcontrib><creatorcontrib>Yoon, Kyong-Ah</creatorcontrib><creatorcontrib>Lee, Kangtaek</creatorcontrib><title>Simultaneous detection of multiple mutations in epidermal growth factor receptor based on fluorescence quenching of quantum dots</title><title>Biosensors &amp; bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>► We develop a simultaneous detection method for multiple mutations. ► We detect two common mutations in the epidermal growth factor receptor gene. ► Fluorescence quenching due to aggregation of quantum dots is used for detection. ► This enables a simultaneous detection of mutations in exon 19 and 21 of EGFR gene. We have developed a simultaneous detection method for two common mutations in the epidermal growth factor receptor gene based on the fluorescence quenching phenomenon caused by aggregation of CdSe quantum dots. For detection of the in-frame deletion in exon 19 and the L858R point mutation in exon 21, water-soluble CdSe quantum dots with two sizes were functionalized using four different types of probe oligonucleotides. Addition of target oligonucleotides with the deletion mutation in exon 19 into the suspensions caused crosslinking-induced aggregation of green-emitting quantum dots, followed by the fluorescence quenching while that with the L858R point mutation resulted in aggregation of yellow-emitting quantum dots. In addition, targets with both deletion and point mutations caused aggregation of both green- and yellow-emitting quantum dots. This method allows a simultaneous detection of mutations in exon 19 and 21 of EGFR gene in a single experiment. We found that minimum mutant concentration that could be detected by this method was as low as 2% for deletion mutation, and 5% for point mutation. PCR products of EGFR gene were also used to confirm that our method could be used to detect mutation in amplified DNA fragments.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>DNA Mutational Analysis - instrumentation</subject><subject>DNA Probes - genetics</subject><subject>Epidermal growth factor receptor</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Fluorescence</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Mutation</subject><subject>Oligonucleotide Array Sequence Analysis - instrumentation</subject><subject>Quantum Dots</subject><subject>Quenching</subject><subject>Receptor, Epidermal Growth Factor - genetics</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Fluorescence - instrumentation</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1TAQhS1ERS-FP8ACeYO6yq1fiROJDarKQ6rEAlhbjj1ufZXEqe1QseOnY-teYAerGR19czQzB6FXlOwpod3VYT_6kPaMUFqEPWHtE7SjveSNYLx9inZkaLum7Tp-jp6ndCCESDqQZ-icMSL7Xogd-vnFz9uU9QJhS9hCBpN9WHBwuOp-naA0WVcxYb9gWL2FOOsJ38XwmO-x0yaHiCMYWGsz6gQWFws3bSFCMrAYwA9bKfd-uavOD5te8jZjG3J6gc6cnhK8PNUL9O39zdfrj83t5w-frt_dNkZQmRtnqKS8E6PWtOuYG7UbGO3bkVBLtRZSWAncOO6kdZo5wQboh5FzIIQ53fILdHn0XWMoy6SsZl92m6bj6WpgpCe87fn_Sco5bQWThWRH0sSQUgSn1uhnHX8oSlSNSB1UjUjViKpWIipDr0_22ziD_TPyO5MCvDkBOhk9uagX49NfrqMFZKxwb48clLd99xBVMr4-2_oSRlY2-H_t8QundbKJ</recordid><startdate>20120115</startdate><enddate>20120115</enddate><creator>Kang, Taegyeong</creator><creator>Lee, Hosub</creator><creator>Choe, Dongcheol</creator><creator>Joo, Sang-Woo</creator><creator>Lee, So Yeong</creator><creator>Yoon, Kyong-Ah</creator><creator>Lee, Kangtaek</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20120115</creationdate><title>Simultaneous detection of multiple mutations in epidermal growth factor receptor based on fluorescence quenching of quantum dots</title><author>Kang, Taegyeong ; Lee, Hosub ; Choe, Dongcheol ; Joo, Sang-Woo ; Lee, So Yeong ; Yoon, Kyong-Ah ; Lee, Kangtaek</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-fc171364baa1662fbaf92185b01d1aa474d7e3cf3f7dfa2f429e89b33e002fa53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>DNA Mutational Analysis - instrumentation</topic><topic>DNA Probes - genetics</topic><topic>Epidermal growth factor receptor</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Fluorescence</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Mutation</topic><topic>Oligonucleotide Array Sequence Analysis - instrumentation</topic><topic>Quantum Dots</topic><topic>Quenching</topic><topic>Receptor, Epidermal Growth Factor - genetics</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Fluorescence - instrumentation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Taegyeong</creatorcontrib><creatorcontrib>Lee, Hosub</creatorcontrib><creatorcontrib>Choe, Dongcheol</creatorcontrib><creatorcontrib>Joo, Sang-Woo</creatorcontrib><creatorcontrib>Lee, So Yeong</creatorcontrib><creatorcontrib>Yoon, Kyong-Ah</creatorcontrib><creatorcontrib>Lee, Kangtaek</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biosensors &amp; bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Taegyeong</au><au>Lee, Hosub</au><au>Choe, Dongcheol</au><au>Joo, Sang-Woo</au><au>Lee, So Yeong</au><au>Yoon, Kyong-Ah</au><au>Lee, Kangtaek</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous detection of multiple mutations in epidermal growth factor receptor based on fluorescence quenching of quantum dots</atitle><jtitle>Biosensors &amp; bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2012-01-15</date><risdate>2012</risdate><volume>31</volume><issue>1</issue><spage>558</spage><epage>561</epage><pages>558-561</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>► We develop a simultaneous detection method for multiple mutations. ► We detect two common mutations in the epidermal growth factor receptor gene. ► Fluorescence quenching due to aggregation of quantum dots is used for detection. ► This enables a simultaneous detection of mutations in exon 19 and 21 of EGFR gene. We have developed a simultaneous detection method for two common mutations in the epidermal growth factor receptor gene based on the fluorescence quenching phenomenon caused by aggregation of CdSe quantum dots. For detection of the in-frame deletion in exon 19 and the L858R point mutation in exon 21, water-soluble CdSe quantum dots with two sizes were functionalized using four different types of probe oligonucleotides. Addition of target oligonucleotides with the deletion mutation in exon 19 into the suspensions caused crosslinking-induced aggregation of green-emitting quantum dots, followed by the fluorescence quenching while that with the L858R point mutation resulted in aggregation of yellow-emitting quantum dots. In addition, targets with both deletion and point mutations caused aggregation of both green- and yellow-emitting quantum dots. This method allows a simultaneous detection of mutations in exon 19 and 21 of EGFR gene in a single experiment. We found that minimum mutant concentration that could be detected by this method was as low as 2% for deletion mutation, and 5% for point mutation. PCR products of EGFR gene were also used to confirm that our method could be used to detect mutation in amplified DNA fragments.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>22078844</pmid><doi>10.1016/j.bios.2011.10.025</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0956-5663
ispartof Biosensors & bioelectronics, 2012-01, Vol.31 (1), p.558-561
issn 0956-5663
1873-4235
language eng
recordid cdi_proquest_miscellaneous_920803583
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Biological and medical sciences
Biotechnology
DNA Mutational Analysis - instrumentation
DNA Probes - genetics
Epidermal growth factor receptor
Equipment Design
Equipment Failure Analysis
Fluorescence
Fundamental and applied biological sciences. Psychology
Mutation
Oligonucleotide Array Sequence Analysis - instrumentation
Quantum Dots
Quenching
Receptor, Epidermal Growth Factor - genetics
Reproducibility of Results
Sensitivity and Specificity
Spectrometry, Fluorescence - instrumentation
title Simultaneous detection of multiple mutations in epidermal growth factor receptor based on fluorescence quenching of quantum dots
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T21%3A48%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Simultaneous%20detection%20of%20multiple%20mutations%20in%20epidermal%20growth%20factor%20receptor%20based%20on%20fluorescence%20quenching%20of%20quantum%20dots&rft.jtitle=Biosensors%20&%20bioelectronics&rft.au=Kang,%20Taegyeong&rft.date=2012-01-15&rft.volume=31&rft.issue=1&rft.spage=558&rft.epage=561&rft.pages=558-561&rft.issn=0956-5663&rft.eissn=1873-4235&rft_id=info:doi/10.1016/j.bios.2011.10.025&rft_dat=%3Cproquest_cross%3E920803583%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=913315427&rft_id=info:pmid/22078844&rft_els_id=S0956566311006932&rfr_iscdi=true