Publication:
Target Induced-DNA strand displacement reaction using gold nanoparticle labeling for hepatitis E virus detection

dc.contributor.authorTatchanun Ngamdeeen_US
dc.contributor.authorLee Su Yinen_US
dc.contributor.authorSompong Vongpunsawaden_US
dc.contributor.authorYong Poovorawanen_US
dc.contributor.authorWerasak Surareungchaien_US
dc.contributor.authorBenchaporn Lertanantawongen_US
dc.contributor.otherAsian Institute of Medicine, Science & Technologyen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherKing Mongkut s University of Technology Thonburien_US
dc.date.accessioned2020-10-05T03:55:01Z
dc.date.available2020-10-05T03:55:01Z
dc.date.issued2020-10-16en_US
dc.description.abstract© 2020 Elsevier B.V. DNA strand displacement is an attractive, enzyme-free target hybridization strategy for nano-biosensing. The target DNA induces a strand displacement reaction by replacing the pre-hybridized strand that is labeled with gold nanoparticles (AuNPs). Thus, the amount of displaced-AuNP-labeled strand is proportional to the amount of target DNA in the sample. The use of a magnetogenosensing technique to isolate the target DNA allows for a simple, one-pot detection approach, which minimizes possible carry-over contamination and pipetting errors. We sought a proof-of-concept for this technology in its ability to detect DNA-equivalent of hepatitis E virus (HEV), which causes acute viral hepatitis for which rapid and simple diagnostic methods remain limited. Signal detection was done via visual observation, spectrophotometry, and electrochemistry. The sensor demonstrated good sensitivity with detection limits of 10 pM (visual), 10 pM (spectrophotometry) and 1 fM (electrochemical). This sensor also exhibited high specificity for real target amplicons and could discriminate between perfect and mismatched sequences. Lyophilized biosensor reagents stored at 4 °C, 25 °C, and outdoor ambient temperature, were stable for up to 90, 50, and 40 days, respectively. The integration of magnetic separation and target DNA-induced strand displacement reaction in a dry reagent form makes the sensing platform easy-to-use and suitable for field settings.en_US
dc.identifier.citationAnalytica Chimica Acta. Vol.1134, (2020), 10-17en_US
dc.identifier.doi10.1016/j.aca.2020.08.018en_US
dc.identifier.issn18734324en_US
dc.identifier.issn00032670en_US
dc.identifier.other2-s2.0-85089810860en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/58945
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089810860&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectEnvironmental Scienceen_US
dc.titleTarget Induced-DNA strand displacement reaction using gold nanoparticle labeling for hepatitis E virus detectionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089810860&origin=inwarden_US

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