Dual-signal amplification strategy for ultrasensitive chemiluminescence detection of PDGF-BB in capillary electrophoresis
Many efforts have been made toward the achievement of high sensitivity in capillary electrophoresis coupled with chemiluminescence detection (CE‐CL). This work describes a novel dual‐signal amplification strategy for highly specific and ultrasensitive CL detection of human platelet‐derived growth fa...
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Veröffentlicht in: | Biomedical chromatography 2015-12, Vol.29 (12), p.1866-1870 |
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creator | Cao, Jun-Tao Wang, Hui Ren, Shu-Wei Chen, Yong-Hong Liu, Yan-Ming |
description | Many efforts have been made toward the achievement of high sensitivity in capillary electrophoresis coupled with chemiluminescence detection (CE‐CL). This work describes a novel dual‐signal amplification strategy for highly specific and ultrasensitive CL detection of human platelet‐derived growth factor–BB (PDGF–BB) using both aptamer and horseradish peroxidase (HRP) modified gold nanoparticles (HRP–AuNPs–aptamer) as nanoprobes in CE. Both AuNPs and HRP in the nanoprobes could amplify the CL signals in the luminol–H2O2 CL system, owing to the excellent catalytic behavior of AuNPs and HRP in the CL system. Meanwhile, the high affinity of aptamer modified on the AuNPs allows detection with high specificity. As proof‐of‐concept, the proposed method was employed to quantify the concentration of PDGF–BB from 0.50 to 250 fm with a detection limit of 0.21 fm. The applicability of the assay was further demonstrated in the analysis of PDGF–BB in human serum samples with acceptable accuracy and reliability. The result of this study exhibits distinct advantages, such as high sensitivity, good specificity, simplicity, and very small sample consumption. The good performances of the proposed strategy provide a powerful avenue for ultrasensitive detection of rare proteins in biological sample, showing great promise in biochemical analysis. Copyright © 2015 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/bmc.3508 |
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This work describes a novel dual‐signal amplification strategy for highly specific and ultrasensitive CL detection of human platelet‐derived growth factor–BB (PDGF–BB) using both aptamer and horseradish peroxidase (HRP) modified gold nanoparticles (HRP–AuNPs–aptamer) as nanoprobes in CE. Both AuNPs and HRP in the nanoprobes could amplify the CL signals in the luminol–H2O2 CL system, owing to the excellent catalytic behavior of AuNPs and HRP in the CL system. Meanwhile, the high affinity of aptamer modified on the AuNPs allows detection with high specificity. As proof‐of‐concept, the proposed method was employed to quantify the concentration of PDGF–BB from 0.50 to 250 fm with a detection limit of 0.21 fm. The applicability of the assay was further demonstrated in the analysis of PDGF–BB in human serum samples with acceptable accuracy and reliability. The result of this study exhibits distinct advantages, such as high sensitivity, good specificity, simplicity, and very small sample consumption. The good performances of the proposed strategy provide a powerful avenue for ultrasensitive detection of rare proteins in biological sample, showing great promise in biochemical analysis. Copyright © 2015 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.3508</identifier><identifier>PMID: 26031509</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>capillary electrophoresis ; chemiluminescence ; Diabetic Nephropathies - blood ; dual signal amplification ; Electrophoresis, Capillary - methods ; Gold - chemistry ; Horseradish Peroxidase - chemistry ; Horseradish Peroxidase - metabolism ; HRP-AuNPs-aptamer ; Humans ; Limit of Detection ; Linear Models ; Luminescent Measurements - methods ; Luminol - chemistry ; Metal Nanoparticles - chemistry ; PDGF-BB ; Proto-Oncogene Proteins c-sis - analysis ; Proto-Oncogene Proteins c-sis - blood ; Proto-Oncogene Proteins c-sis - chemistry ; Reproducibility of Results ; Signal Processing, Computer-Assisted</subject><ispartof>Biomedical chromatography, 2015-12, Vol.29 (12), p.1866-1870</ispartof><rights>Copyright © 2015 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4298-1dd8e8ec3816e62c80379c86f4eb120dd704e9209caf801e92674aff9bbbf7a83</citedby><cites>FETCH-LOGICAL-c4298-1dd8e8ec3816e62c80379c86f4eb120dd704e9209caf801e92674aff9bbbf7a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbmc.3508$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.3508$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26031509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Jun-Tao</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Ren, Shu-Wei</creatorcontrib><creatorcontrib>Chen, Yong-Hong</creatorcontrib><creatorcontrib>Liu, Yan-Ming</creatorcontrib><title>Dual-signal amplification strategy for ultrasensitive chemiluminescence detection of PDGF-BB in capillary electrophoresis</title><title>Biomedical chromatography</title><addtitle>Biomed. Chromatogr</addtitle><description>Many efforts have been made toward the achievement of high sensitivity in capillary electrophoresis coupled with chemiluminescence detection (CE‐CL). This work describes a novel dual‐signal amplification strategy for highly specific and ultrasensitive CL detection of human platelet‐derived growth factor–BB (PDGF–BB) using both aptamer and horseradish peroxidase (HRP) modified gold nanoparticles (HRP–AuNPs–aptamer) as nanoprobes in CE. Both AuNPs and HRP in the nanoprobes could amplify the CL signals in the luminol–H2O2 CL system, owing to the excellent catalytic behavior of AuNPs and HRP in the CL system. Meanwhile, the high affinity of aptamer modified on the AuNPs allows detection with high specificity. As proof‐of‐concept, the proposed method was employed to quantify the concentration of PDGF–BB from 0.50 to 250 fm with a detection limit of 0.21 fm. The applicability of the assay was further demonstrated in the analysis of PDGF–BB in human serum samples with acceptable accuracy and reliability. The result of this study exhibits distinct advantages, such as high sensitivity, good specificity, simplicity, and very small sample consumption. The good performances of the proposed strategy provide a powerful avenue for ultrasensitive detection of rare proteins in biological sample, showing great promise in biochemical analysis. Copyright © 2015 John Wiley & Sons, Ltd.</description><subject>capillary electrophoresis</subject><subject>chemiluminescence</subject><subject>Diabetic Nephropathies - blood</subject><subject>dual signal amplification</subject><subject>Electrophoresis, Capillary - methods</subject><subject>Gold - chemistry</subject><subject>Horseradish Peroxidase - chemistry</subject><subject>Horseradish Peroxidase - metabolism</subject><subject>HRP-AuNPs-aptamer</subject><subject>Humans</subject><subject>Limit of Detection</subject><subject>Linear Models</subject><subject>Luminescent Measurements - methods</subject><subject>Luminol - chemistry</subject><subject>Metal Nanoparticles - chemistry</subject><subject>PDGF-BB</subject><subject>Proto-Oncogene Proteins c-sis - analysis</subject><subject>Proto-Oncogene Proteins c-sis - blood</subject><subject>Proto-Oncogene Proteins c-sis - chemistry</subject><subject>Reproducibility of Results</subject><subject>Signal Processing, Computer-Assisted</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1vEzEQhi0EomlB4hcgH7lsGdvJ2j6SlAaktnAocLS83nFr8H5g70Lz73FpWvXS03ikx6_eeQh5w-CYAfD3TeeOxQrUM7JgoHUFCthzsgBe60ooqQ_IYc4_AUDXXL4kB7wGwVagF2R3MttY5XDV20htN8bgg7NTGHqap2QnvNpRPyQ6x7Jl7HOYwh-k7hq7EOcu9Jgd9g5pixO6__8GT7-ebE-r9ZqGnjo7hhht2lGMBUjDeD0kzCG_Ii-8jRlf7-cR-Xb68XLzqTr7sv28-XBWuSXXqmJtq1ChE4rVWHOnQEjtVO2X2DAObSthiZqDdtaXq8uzlkvrvW6axkurxBF5d5c7puH3jHkyXSidS6cehzkbJrnUWkD9CHVpyDmhN2MKXeluGJhb0aaINreiC_p2nzo3HbYP4L3ZAlR3wN8QcfdkkFmfb_aBez7kCW8eeJt-mVoKuTI_LrbmQkn1netLA-Ifp1OYbg</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Cao, Jun-Tao</creator><creator>Wang, Hui</creator><creator>Ren, Shu-Wei</creator><creator>Chen, Yong-Hong</creator><creator>Liu, Yan-Ming</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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></search><sort><creationdate>201512</creationdate><title>Dual-signal amplification strategy for ultrasensitive chemiluminescence detection of PDGF-BB in capillary electrophoresis</title><author>Cao, Jun-Tao ; Wang, Hui ; Ren, Shu-Wei ; Chen, Yong-Hong ; Liu, Yan-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4298-1dd8e8ec3816e62c80379c86f4eb120dd704e9209caf801e92674aff9bbbf7a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>capillary electrophoresis</topic><topic>chemiluminescence</topic><topic>Diabetic Nephropathies - blood</topic><topic>dual signal amplification</topic><topic>Electrophoresis, Capillary - methods</topic><topic>Gold - chemistry</topic><topic>Horseradish Peroxidase - chemistry</topic><topic>Horseradish Peroxidase - metabolism</topic><topic>HRP-AuNPs-aptamer</topic><topic>Humans</topic><topic>Limit of Detection</topic><topic>Linear Models</topic><topic>Luminescent Measurements - methods</topic><topic>Luminol - chemistry</topic><topic>Metal Nanoparticles - chemistry</topic><topic>PDGF-BB</topic><topic>Proto-Oncogene Proteins c-sis - analysis</topic><topic>Proto-Oncogene Proteins c-sis - blood</topic><topic>Proto-Oncogene Proteins c-sis - chemistry</topic><topic>Reproducibility of Results</topic><topic>Signal Processing, Computer-Assisted</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Jun-Tao</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Ren, Shu-Wei</creatorcontrib><creatorcontrib>Chen, Yong-Hong</creatorcontrib><creatorcontrib>Liu, Yan-Ming</creatorcontrib><collection>Istex</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><jtitle>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Jun-Tao</au><au>Wang, Hui</au><au>Ren, Shu-Wei</au><au>Chen, Yong-Hong</au><au>Liu, Yan-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dual-signal amplification strategy for ultrasensitive chemiluminescence detection of PDGF-BB in capillary electrophoresis</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed. Chromatogr</addtitle><date>2015-12</date><risdate>2015</risdate><volume>29</volume><issue>12</issue><spage>1866</spage><epage>1870</epage><pages>1866-1870</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>Many efforts have been made toward the achievement of high sensitivity in capillary electrophoresis coupled with chemiluminescence detection (CE‐CL). This work describes a novel dual‐signal amplification strategy for highly specific and ultrasensitive CL detection of human platelet‐derived growth factor–BB (PDGF–BB) using both aptamer and horseradish peroxidase (HRP) modified gold nanoparticles (HRP–AuNPs–aptamer) as nanoprobes in CE. Both AuNPs and HRP in the nanoprobes could amplify the CL signals in the luminol–H2O2 CL system, owing to the excellent catalytic behavior of AuNPs and HRP in the CL system. Meanwhile, the high affinity of aptamer modified on the AuNPs allows detection with high specificity. As proof‐of‐concept, the proposed method was employed to quantify the concentration of PDGF–BB from 0.50 to 250 fm with a detection limit of 0.21 fm. The applicability of the assay was further demonstrated in the analysis of PDGF–BB in human serum samples with acceptable accuracy and reliability. The result of this study exhibits distinct advantages, such as high sensitivity, good specificity, simplicity, and very small sample consumption. The good performances of the proposed strategy provide a powerful avenue for ultrasensitive detection of rare proteins in biological sample, showing great promise in biochemical analysis. Copyright © 2015 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26031509</pmid><doi>10.1002/bmc.3508</doi><tpages>5</tpages></addata></record> |
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subjects | capillary electrophoresis chemiluminescence Diabetic Nephropathies - blood dual signal amplification Electrophoresis, Capillary - methods Gold - chemistry Horseradish Peroxidase - chemistry Horseradish Peroxidase - metabolism HRP-AuNPs-aptamer Humans Limit of Detection Linear Models Luminescent Measurements - methods Luminol - chemistry Metal Nanoparticles - chemistry PDGF-BB Proto-Oncogene Proteins c-sis - analysis Proto-Oncogene Proteins c-sis - blood Proto-Oncogene Proteins c-sis - chemistry Reproducibility of Results Signal Processing, Computer-Assisted |
title | Dual-signal amplification strategy for ultrasensitive chemiluminescence detection of PDGF-BB in capillary electrophoresis |
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