PCR-Free Colorimetric DNA Hybridization Detection Using a 3D DNA Nanostructured Reporter Probe
A “sandwich-like” biosensor was developed on the basis of the magnetic bead platform for sensitive detection of breast cancer 1 (BRCA1) DNA. In the present study, a tetrahedron-structured reporter probe (TSRP) was designed, in which 3 vertices of the tetrahedron were labeled with digoxin (Dig), and...
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Veröffentlicht in: | ACS applied materials & interfaces 2017-11, Vol.9 (44), p.38281-38287 |
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container_title | ACS applied materials & interfaces |
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creator | Yang, Xue Wen, Yanli Wang, Lele Zhou, Chaoqun Li, Qian Xu, Li Li, Lanying Shi, Jiye Lal, Ratnesh Ren, Shuzhen Li, Jiang Jia, Nengqin Liu, Gang |
description | A “sandwich-like” biosensor was developed on the basis of the magnetic bead platform for sensitive detection of breast cancer 1 (BRCA1) DNA. In the present study, a tetrahedron-structured reporter probe (TSRP) was designed, in which 3 vertices of the tetrahedron were labeled with digoxin (Dig), and the other one was labeled with a detection probe. TSRP here provided accurate enzyme loading and well-organized spatial arrangement for optimized signal amplification. The detection limit of this biosensor was as low as 10 fM, which is at least 4 orders of magnitude lower than that of the single DNA probe (100 pM), and the signal gain was 2 times higher than the analysis using three one-dimensional (1D) reporter probes. We could distinguish DNA sequences with only 1 base mismatch, and the performance of our TSRP biosensor was proven to be equally good in both PCR products and real fetal calf serum (FCS) sample as in buffer. We believe this work provided a novel avenue for the development of signal amplification strategies. |
doi_str_mv | 10.1021/acsami.7b11994 |
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In the present study, a tetrahedron-structured reporter probe (TSRP) was designed, in which 3 vertices of the tetrahedron were labeled with digoxin (Dig), and the other one was labeled with a detection probe. TSRP here provided accurate enzyme loading and well-organized spatial arrangement for optimized signal amplification. The detection limit of this biosensor was as low as 10 fM, which is at least 4 orders of magnitude lower than that of the single DNA probe (100 pM), and the signal gain was 2 times higher than the analysis using three one-dimensional (1D) reporter probes. We could distinguish DNA sequences with only 1 base mismatch, and the performance of our TSRP biosensor was proven to be equally good in both PCR products and real fetal calf serum (FCS) sample as in buffer. We believe this work provided a novel avenue for the development of signal amplification strategies.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.7b11994</identifier><identifier>PMID: 29022698</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Biosensing Techniques ; Colorimetry ; DNA Probes - chemistry ; Nanostructures ; Nucleic Acid Hybridization ; Polymerase Chain Reaction</subject><ispartof>ACS applied materials & interfaces, 2017-11, Vol.9 (44), p.38281-38287</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a330t-515ce56e718d588929a8bb3be3dd33c9b7476cf6725d0b37790e5c4d13ce77e83</citedby><cites>FETCH-LOGICAL-a330t-515ce56e718d588929a8bb3be3dd33c9b7476cf6725d0b37790e5c4d13ce77e83</cites><orcidid>0000-0003-2372-6624 ; 0000-0003-3779-7212 ; 0000-0003-1086-0998 ; 0000-0003-0761-8877</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.7b11994$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.7b11994$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29022698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Xue</creatorcontrib><creatorcontrib>Wen, Yanli</creatorcontrib><creatorcontrib>Wang, Lele</creatorcontrib><creatorcontrib>Zhou, Chaoqun</creatorcontrib><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Xu, Li</creatorcontrib><creatorcontrib>Li, Lanying</creatorcontrib><creatorcontrib>Shi, Jiye</creatorcontrib><creatorcontrib>Lal, Ratnesh</creatorcontrib><creatorcontrib>Ren, Shuzhen</creatorcontrib><creatorcontrib>Li, Jiang</creatorcontrib><creatorcontrib>Jia, Nengqin</creatorcontrib><creatorcontrib>Liu, Gang</creatorcontrib><title>PCR-Free Colorimetric DNA Hybridization Detection Using a 3D DNA Nanostructured Reporter Probe</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>A “sandwich-like” biosensor was developed on the basis of the magnetic bead platform for sensitive detection of breast cancer 1 (BRCA1) DNA. In the present study, a tetrahedron-structured reporter probe (TSRP) was designed, in which 3 vertices of the tetrahedron were labeled with digoxin (Dig), and the other one was labeled with a detection probe. TSRP here provided accurate enzyme loading and well-organized spatial arrangement for optimized signal amplification. The detection limit of this biosensor was as low as 10 fM, which is at least 4 orders of magnitude lower than that of the single DNA probe (100 pM), and the signal gain was 2 times higher than the analysis using three one-dimensional (1D) reporter probes. We could distinguish DNA sequences with only 1 base mismatch, and the performance of our TSRP biosensor was proven to be equally good in both PCR products and real fetal calf serum (FCS) sample as in buffer. 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Mater. Interfaces</addtitle><date>2017-11-08</date><risdate>2017</risdate><volume>9</volume><issue>44</issue><spage>38281</spage><epage>38287</epage><pages>38281-38287</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>A “sandwich-like” biosensor was developed on the basis of the magnetic bead platform for sensitive detection of breast cancer 1 (BRCA1) DNA. In the present study, a tetrahedron-structured reporter probe (TSRP) was designed, in which 3 vertices of the tetrahedron were labeled with digoxin (Dig), and the other one was labeled with a detection probe. TSRP here provided accurate enzyme loading and well-organized spatial arrangement for optimized signal amplification. The detection limit of this biosensor was as low as 10 fM, which is at least 4 orders of magnitude lower than that of the single DNA probe (100 pM), and the signal gain was 2 times higher than the analysis using three one-dimensional (1D) reporter probes. We could distinguish DNA sequences with only 1 base mismatch, and the performance of our TSRP biosensor was proven to be equally good in both PCR products and real fetal calf serum (FCS) sample as in buffer. We believe this work provided a novel avenue for the development of signal amplification strategies.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29022698</pmid><doi>10.1021/acsami.7b11994</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-2372-6624</orcidid><orcidid>https://orcid.org/0000-0003-3779-7212</orcidid><orcidid>https://orcid.org/0000-0003-1086-0998</orcidid><orcidid>https://orcid.org/0000-0003-0761-8877</orcidid></addata></record> |
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subjects | Biosensing Techniques Colorimetry DNA Probes - chemistry Nanostructures Nucleic Acid Hybridization Polymerase Chain Reaction |
title | PCR-Free Colorimetric DNA Hybridization Detection Using a 3D DNA Nanostructured Reporter Probe |
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