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Proximity extension of circular DNA aptamers with real-time protein detection
Multivalent circular aptamers or ‘captamers’ have recently been introduced through the merger of aptameric recognition functions with the basic principles of DNA nanotechnology. Aptamers have strong utility as protein-binding motifs for diagnostic applications, where their ease of discovery, thermal...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1074748/ https://www.ncbi.nlm.nih.gov/pubmed/15817563 http://dx.doi.org/10.1093/nar/gni063 |
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author | Di Giusto, Daniel A. Wlassoff, Wjatschesslaw A. Gooding, J. Justin Messerle, Barbara A. King, Garry C. |
author_facet | Di Giusto, Daniel A. Wlassoff, Wjatschesslaw A. Gooding, J. Justin Messerle, Barbara A. King, Garry C. |
author_sort | Di Giusto, Daniel A. |
collection | PubMed |
description | Multivalent circular aptamers or ‘captamers’ have recently been introduced through the merger of aptameric recognition functions with the basic principles of DNA nanotechnology. Aptamers have strong utility as protein-binding motifs for diagnostic applications, where their ease of discovery, thermal stability and low cost make them ideal components for incorporation into targeted protein assays. Here we report upon a property specific to circular DNA aptamers: their intrinsic compatibility with a highly sensitive protein detection method termed the ‘proximity extension’ assay. The circular DNA architecture facilitates the integration of multiple functional elements into a single molecule: aptameric target recognition, nucleic acid hybridization specificity and rolling circle amplification. Successful exploitation of these properties is demonstrated for the molecular analysis of thrombin, with the assay delivering a detection limit nearly three orders of magnitude below the dissociation constants of the two contributing aptamer–thrombin interactions. Real-time signal amplification and detection under isothermal conditions points towards potential clinical applications, with both fluorescent and bioelectronic methods of detection achieved. This application elaborates the pleiotropic properties of circular DNA aptamers beyond the stability, potency and multitargeting characteristics described earlier. |
format | Text |
id | pubmed-1074748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-10747482005-04-08 Proximity extension of circular DNA aptamers with real-time protein detection Di Giusto, Daniel A. Wlassoff, Wjatschesslaw A. Gooding, J. Justin Messerle, Barbara A. King, Garry C. Nucleic Acids Res Methods Online Multivalent circular aptamers or ‘captamers’ have recently been introduced through the merger of aptameric recognition functions with the basic principles of DNA nanotechnology. Aptamers have strong utility as protein-binding motifs for diagnostic applications, where their ease of discovery, thermal stability and low cost make them ideal components for incorporation into targeted protein assays. Here we report upon a property specific to circular DNA aptamers: their intrinsic compatibility with a highly sensitive protein detection method termed the ‘proximity extension’ assay. The circular DNA architecture facilitates the integration of multiple functional elements into a single molecule: aptameric target recognition, nucleic acid hybridization specificity and rolling circle amplification. Successful exploitation of these properties is demonstrated for the molecular analysis of thrombin, with the assay delivering a detection limit nearly three orders of magnitude below the dissociation constants of the two contributing aptamer–thrombin interactions. Real-time signal amplification and detection under isothermal conditions points towards potential clinical applications, with both fluorescent and bioelectronic methods of detection achieved. This application elaborates the pleiotropic properties of circular DNA aptamers beyond the stability, potency and multitargeting characteristics described earlier. Oxford University Press 2005 2005-04-07 /pmc/articles/PMC1074748/ /pubmed/15817563 http://dx.doi.org/10.1093/nar/gni063 Text en © The Author 2005. Published by Oxford University Press. All rights reserved |
spellingShingle | Methods Online Di Giusto, Daniel A. Wlassoff, Wjatschesslaw A. Gooding, J. Justin Messerle, Barbara A. King, Garry C. Proximity extension of circular DNA aptamers with real-time protein detection |
title | Proximity extension of circular DNA aptamers with real-time protein detection |
title_full | Proximity extension of circular DNA aptamers with real-time protein detection |
title_fullStr | Proximity extension of circular DNA aptamers with real-time protein detection |
title_full_unstemmed | Proximity extension of circular DNA aptamers with real-time protein detection |
title_short | Proximity extension of circular DNA aptamers with real-time protein detection |
title_sort | proximity extension of circular dna aptamers with real-time protein detection |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1074748/ https://www.ncbi.nlm.nih.gov/pubmed/15817563 http://dx.doi.org/10.1093/nar/gni063 |
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