Novel signal amplification approach for HRP-based colorimetric genosensors using DNA binding protein tags
The need for sensitive detection of DNA is growing as more specific DNA sequences are being correlated to gene markers for disease diagnosis, food safety and other security related applications. Detection in hybridization-based assays is usually achieved with target-specific ssDNA probes conjugated...
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Veröffentlicht in: | Biosensors & bioelectronics 2015-12, Vol.74, p.1005-1010 |
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description | The need for sensitive detection of DNA is growing as more specific DNA sequences are being correlated to gene markers for disease diagnosis, food safety and other security related applications. Detection in hybridization-based assays is usually achieved with target-specific ssDNA probes conjugated directly to enzyme labels like HRP that provide signal amplification or with nanoparticles functionalized with DNA and multiple HRP molecules. In order to overcome some of the drawbacks presented by these approaches, we developed a unique DNA sensing platform based on an HRP–DNA binding protein tag conjugate and a hybrid ssDNA–dsDNA detection probe. Specifically, in this work we describe the preparation and characterization of an HRP conjugate with scCro DNA binding protein tag and its application for the detection of a model ssDNA target sequence. By using the HRP–scCro conjugate together with a hybrid detection probe containing three scCro‐specific dsDNA binding sites, we demonstrate an improvement by over 3-fold in both sensitivity and limit of detection of high-risk human papillomavirus (HPV16), compared to the standard ssDNA–HRP conjugate. These results show that the HRP–DNA binding protein tag conjugate can be used as an alternative and universal tool for signal enhancement in enzyme-linked assays suitable for integration in point-of-care systems. |
doi_str_mv | 10.1016/j.bios.2015.07.077 |
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Detection in hybridization-based assays is usually achieved with target-specific ssDNA probes conjugated directly to enzyme labels like HRP that provide signal amplification or with nanoparticles functionalized with DNA and multiple HRP molecules. In order to overcome some of the drawbacks presented by these approaches, we developed a unique DNA sensing platform based on an HRP–DNA binding protein tag conjugate and a hybrid ssDNA–dsDNA detection probe. Specifically, in this work we describe the preparation and characterization of an HRP conjugate with scCro DNA binding protein tag and its application for the detection of a model ssDNA target sequence. By using the HRP–scCro conjugate together with a hybrid detection probe containing three scCro‐specific dsDNA binding sites, we demonstrate an improvement by over 3-fold in both sensitivity and limit of detection of high-risk human papillomavirus (HPV16), compared to the standard ssDNA–HRP conjugate. These results show that the HRP–DNA binding protein tag conjugate can be used as an alternative and universal tool for signal enhancement in enzyme-linked assays suitable for integration in point-of-care systems.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2015.07.077</identifier><identifier>PMID: 26264267</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Amplification ; Assaying ; Binding ; Chromosome Mapping - instrumentation ; Colorimetry - instrumentation ; Conjugates ; Deoxyribonucleic acid ; DNA - analysis ; DNA - chemistry ; DNA - genetics ; DNA binding protein ; DNA detection ; DNA-Binding Proteins - chemistry ; ELONA ; Enzyme-linked assay ; Enzyme-Linked Immunosorbent Assay - instrumentation ; Equipment Design ; Equipment Failure Analysis ; Gene sequencing ; Genosensor ; Horseradish Peroxidase - chemistry ; Human papillomavirus ; Human papillomavirus 16 ; Mathematical models ; Point-of-Care Systems ; Proteins ; Sequence Analysis, DNA - instrumentation ; Sequence Analysis, DNA - methods ; Signal amplification</subject><ispartof>Biosensors & bioelectronics, 2015-12, Vol.74, p.1005-1010</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-4c9135c6be97263eb95eefa054e866c7982408ea1be2b8b91b73b3e04ce4d513</citedby><cites>FETCH-LOGICAL-c422t-4c9135c6be97263eb95eefa054e866c7982408ea1be2b8b91b73b3e04ce4d513</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.2015.07.077$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26264267$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aktas, Gülsen Betül</creatorcontrib><creatorcontrib>Skouridou, Vasso</creatorcontrib><creatorcontrib>Masip, Lluis</creatorcontrib><title>Novel signal amplification approach for HRP-based colorimetric genosensors using DNA binding protein tags</title><title>Biosensors & bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>The need for sensitive detection of DNA is growing as more specific DNA sequences are being correlated to gene markers for disease diagnosis, food safety and other security related applications. Detection in hybridization-based assays is usually achieved with target-specific ssDNA probes conjugated directly to enzyme labels like HRP that provide signal amplification or with nanoparticles functionalized with DNA and multiple HRP molecules. In order to overcome some of the drawbacks presented by these approaches, we developed a unique DNA sensing platform based on an HRP–DNA binding protein tag conjugate and a hybrid ssDNA–dsDNA detection probe. Specifically, in this work we describe the preparation and characterization of an HRP conjugate with scCro DNA binding protein tag and its application for the detection of a model ssDNA target sequence. By using the HRP–scCro conjugate together with a hybrid detection probe containing three scCro‐specific dsDNA binding sites, we demonstrate an improvement by over 3-fold in both sensitivity and limit of detection of high-risk human papillomavirus (HPV16), compared to the standard ssDNA–HRP conjugate. These results show that the HRP–DNA binding protein tag conjugate can be used as an alternative and universal tool for signal enhancement in enzyme-linked assays suitable for integration in point-of-care systems.</description><subject>Amplification</subject><subject>Assaying</subject><subject>Binding</subject><subject>Chromosome Mapping - instrumentation</subject><subject>Colorimetry - instrumentation</subject><subject>Conjugates</subject><subject>Deoxyribonucleic acid</subject><subject>DNA - analysis</subject><subject>DNA - chemistry</subject><subject>DNA - genetics</subject><subject>DNA binding protein</subject><subject>DNA detection</subject><subject>DNA-Binding Proteins - chemistry</subject><subject>ELONA</subject><subject>Enzyme-linked assay</subject><subject>Enzyme-Linked Immunosorbent Assay - instrumentation</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Gene sequencing</subject><subject>Genosensor</subject><subject>Horseradish Peroxidase - chemistry</subject><subject>Human papillomavirus</subject><subject>Human papillomavirus 16</subject><subject>Mathematical models</subject><subject>Point-of-Care Systems</subject><subject>Proteins</subject><subject>Sequence Analysis, DNA - instrumentation</subject><subject>Sequence Analysis, DNA - methods</subject><subject>Signal amplification</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV9rFDEUxYModlv9Aj5IHn2ZNcnkzwR8Ka1aoVSRvockc2fNMpusubMFv71ZtvZRChfuffidc-EcQt5xtuaM64_bdUgF14JxtWamjXlBVnwwfSdFr16SFbNKd0rr_oycI24ZY4Zb9pqcCS20FNqsSLorDzBTTJvsZ-p3-zlNKfollUz9fl-Lj7_oVCq9-fmjCx5hpLHMpaYdLDVFuoFcEDKWivSAKW_o9d0lDSmPx7vpF0iZLn6Db8iryc8Ibx_3Bbn_8vn-6qa7_f7129XlbRelEEsno-W9ijqANUL3EKwCmDxTEgato7GDkGwAzwOIMATLg-lDD0xGkKPi_QX5cLJtv38fABe3Sxhhnn2GckDHjZTaGj6IZ6BcqEaq56BMK2OUVQ0VJzTWglhhcvuWlq9_HGfu2JvbumNv7tibY6aNaaL3j_6HsIPxSfKvqAZ8OgHQontIUB3GBDnCmCrExY0l_c__L9lQqaY</recordid><startdate>20151215</startdate><enddate>20151215</enddate><creator>Aktas, Gülsen Betül</creator><creator>Skouridou, Vasso</creator><creator>Masip, Lluis</creator><general>Elsevier B.V</general><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SP</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>20151215</creationdate><title>Novel signal amplification approach for HRP-based colorimetric genosensors using DNA binding protein tags</title><author>Aktas, Gülsen Betül ; Skouridou, Vasso ; Masip, Lluis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-4c9135c6be97263eb95eefa054e866c7982408ea1be2b8b91b73b3e04ce4d513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amplification</topic><topic>Assaying</topic><topic>Binding</topic><topic>Chromosome Mapping - instrumentation</topic><topic>Colorimetry - instrumentation</topic><topic>Conjugates</topic><topic>Deoxyribonucleic acid</topic><topic>DNA - analysis</topic><topic>DNA - chemistry</topic><topic>DNA - genetics</topic><topic>DNA binding protein</topic><topic>DNA detection</topic><topic>DNA-Binding Proteins - chemistry</topic><topic>ELONA</topic><topic>Enzyme-linked assay</topic><topic>Enzyme-Linked Immunosorbent Assay - instrumentation</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Gene sequencing</topic><topic>Genosensor</topic><topic>Horseradish Peroxidase - chemistry</topic><topic>Human papillomavirus</topic><topic>Human papillomavirus 16</topic><topic>Mathematical models</topic><topic>Point-of-Care Systems</topic><topic>Proteins</topic><topic>Sequence Analysis, DNA - instrumentation</topic><topic>Sequence Analysis, DNA - methods</topic><topic>Signal amplification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aktas, Gülsen Betül</creatorcontrib><creatorcontrib>Skouridou, Vasso</creatorcontrib><creatorcontrib>Masip, Lluis</creatorcontrib><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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aktas, Gülsen Betül</au><au>Skouridou, Vasso</au><au>Masip, Lluis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel signal amplification approach for HRP-based colorimetric genosensors using DNA binding protein tags</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2015-12-15</date><risdate>2015</risdate><volume>74</volume><spage>1005</spage><epage>1010</epage><pages>1005-1010</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>The need for sensitive detection of DNA is growing as more specific DNA sequences are being correlated to gene markers for disease diagnosis, food safety and other security related applications. Detection in hybridization-based assays is usually achieved with target-specific ssDNA probes conjugated directly to enzyme labels like HRP that provide signal amplification or with nanoparticles functionalized with DNA and multiple HRP molecules. In order to overcome some of the drawbacks presented by these approaches, we developed a unique DNA sensing platform based on an HRP–DNA binding protein tag conjugate and a hybrid ssDNA–dsDNA detection probe. Specifically, in this work we describe the preparation and characterization of an HRP conjugate with scCro DNA binding protein tag and its application for the detection of a model ssDNA target sequence. By using the HRP–scCro conjugate together with a hybrid detection probe containing three scCro‐specific dsDNA binding sites, we demonstrate an improvement by over 3-fold in both sensitivity and limit of detection of high-risk human papillomavirus (HPV16), compared to the standard ssDNA–HRP conjugate. 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subjects | Amplification Assaying Binding Chromosome Mapping - instrumentation Colorimetry - instrumentation Conjugates Deoxyribonucleic acid DNA - analysis DNA - chemistry DNA - genetics DNA binding protein DNA detection DNA-Binding Proteins - chemistry ELONA Enzyme-linked assay Enzyme-Linked Immunosorbent Assay - instrumentation Equipment Design Equipment Failure Analysis Gene sequencing Genosensor Horseradish Peroxidase - chemistry Human papillomavirus Human papillomavirus 16 Mathematical models Point-of-Care Systems Proteins Sequence Analysis, DNA - instrumentation Sequence Analysis, DNA - methods Signal amplification |
title | Novel signal amplification approach for HRP-based colorimetric genosensors using DNA binding protein tags |
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