Please use this identifier to cite or link to this item: https://doi.org/10.1093/nar/gku655
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dc.titleEngineering self-contained DNA circuit for proximity recognition and localized signal amplification of target biomolecules
dc.contributor.authorAng, Yan Shan
dc.contributor.authorYung, Lin-Yue Lanry
dc.date.accessioned2020-05-29T09:59:09Z
dc.date.available2020-05-29T09:59:09Z
dc.date.issued2014-01-01
dc.identifier.citationAng, Yan Shan, Yung, Lin-Yue Lanry (2014-01-01). Engineering self-contained DNA circuit for proximity recognition and localized signal amplification of target biomolecules. NUCLEIC ACIDS RESEARCH 42 (14) : 9523-9530. ScholarBank@NUS Repository. https://doi.org/10.1093/nar/gku655
dc.identifier.issn03051048
dc.identifier.issn13624962
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/168697
dc.description.abstractBiomolecular interactions have important cellular implications, however, a simple method for the sensing of such proximal events is lacking in the current molecular toolbox. We designed a dynamic DNA circuit capable of recognizing targets in close proximity to initiate a pre-programmed signal transduction process resulting in localized signal amplification. The entire circuitwas engineered to be self-contained, i.e. it can self-assemble onto individual target molecules autonomously and form localized signal withminimal cross-talk. α-thrombin was used as a model protein to evaluate the performance of the individual modules and the overall circuit for proximity interaction under physiologically relevant buffer condition. The circuit achieved good selectivity in presence of nonspecific protein and interfering serum matrix and successfully detected for physiologically relevant α-thrombin concentration (50 nM-5 μM) in a singlemixing step without any further washing. The formation of localized signal at the interaction site can be enhanced kinetically through the control of temperature and probe concentration. This work provides a basic general framework from which other circuit modules can be adapted for the sensing of other biomolecular or cellular interaction of interest. © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research.
dc.language.isoen
dc.publisherOXFORD UNIV PRESS
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiochemistry & Molecular Biology
dc.subjectIN-SITU
dc.typeArticle
dc.date.updated2020-05-27T16:32:06Z
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1093/nar/gku655
dc.description.sourcetitleNUCLEIC ACIDS RESEARCH
dc.description.volume42
dc.description.issue14
dc.description.page9523-9530
dc.published.statePublished
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