Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-018-05733-0
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dc.titleVisual and modular detection of pathogen nucleic acids with enzyme–DNA molecular complexes
dc.contributor.authorHo, N.R.Y
dc.contributor.authorLim, G.S
dc.contributor.authorSundah, N.R
dc.contributor.authorLim, D
dc.contributor.authorLoh, T.P
dc.contributor.authorShao, H
dc.date.accessioned2020-09-04T01:46:18Z
dc.date.available2020-09-04T01:46:18Z
dc.date.issued2018
dc.identifier.citationHo, N.R.Y, Lim, G.S, Sundah, N.R, Lim, D, Loh, T.P, Shao, H (2018). Visual and modular detection of pathogen nucleic acids with enzyme–DNA molecular complexes. Nature Communications 9 (1) : 3238. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-018-05733-0
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174207
dc.description.abstractRapid, visual detection of pathogen nucleic acids has broad applications in infection management. Here we present a modular detection platform, termed enzyme-assisted nanocomplexes for visual identification of nucleic acids (enVision). The system consists of an integrated circuit of enzyme–DNA nanostructures, which function as independent recognition and signaling elements, for direct and versatile detection of pathogen nucleic acids from infected cells. The built-in enzymatic cascades produce a rapid color readout for the naked eye; the assay is thus fast (<2 h), sensitive (<10 amol), and readily quantified with smartphones. When implemented on a configurable microfluidic platform, the technology demonstrates superior programmability to perform versatile computations, for detecting diverse pathogen targets and their virus–host genome integration loci. We further design the enVision platform for molecular-typing of infections in patient endocervical samples. The technology not only improves the clinical inter-subtype differentiation, but also expands the intra-subtype coverage to identify previously undetectable infections. © 2018, The Author(s).
dc.publisherNature Publishing Group
dc.sourceUnpaywall 20200831
dc.subjectDNA
dc.subjectenzyme
dc.subjectgenomic DNA
dc.subjectnucleic acid
dc.subjectvirus DNA
dc.subjectvirus RNA
dc.subjectDNA
dc.subjecthorseradish peroxidase
dc.subjectnanomaterial
dc.subjectnucleic acid
dc.subjectcell
dc.subjectdetection method
dc.subjectDNA
dc.subjectenzyme
dc.subjectgenome
dc.subjectmolecular analysis
dc.subjectnanoparticle
dc.subjectnucleic acid
dc.subjectpathogen
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectDNA conformation
dc.subjectDNA structure
dc.subjectenzyme activity
dc.subjectfalse positive result
dc.subjectfemale
dc.subjectgene locus
dc.subjecthuman
dc.subjecthuman cell
dc.subjectHuman papillomavirus type 16
dc.subjectHuman papillomavirus type 18
dc.subjectlimit of detection
dc.subjectmicrofluidics
dc.subjectmolecular recognition
dc.subjectmolecular typing
dc.subjectnonhuman
dc.subjectnucleic acid analysis
dc.subjectpolymerase chain reaction
dc.subjectsignal detection
dc.subjectvirus genome
dc.subjectbioassay
dc.subjectchemistry
dc.subjectgenetics
dc.subjectisolation and purification
dc.subjectmetabolism
dc.subjectPapillomaviridae
dc.subjectBiological Assay
dc.subjectDNA
dc.subjectHorseradish Peroxidase
dc.subjectHumans
dc.subjectNanostructures
dc.subjectNucleic Acids
dc.subjectPapillomaviridae
dc.typeArticle
dc.contributor.departmentBIOMED INST FOR GLOBAL HEALTH RES & TECH
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.description.doi10.1038/s41467-018-05733-0
dc.description.sourcetitleNature Communications
dc.description.volume9
dc.description.issue1
dc.description.page3238
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