Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/70512
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorShi, JYen_US
dc.creatorLyu, Jen_US
dc.creatorTian, Fen_US
dc.creatorYang, Men_US
dc.date.accessioned2017-12-28T06:17:07Z-
dc.date.available2017-12-28T06:17:07Z-
dc.identifier.issn0956-5663en_US
dc.identifier.urihttp://hdl.handle.net/10397/70512-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2016 Elsevier B.V. All rights reserved.en_US
dc.rights© 2016. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.rightsThe following publication Shi, J., Lyu, J., Tian, F., & Yang, M. (2017). A fluorescence turn-on biosensor based on graphene quantum dots (GQDs) and molybdenum disulfide (MoS2) nanosheets for epithelial cell adhesion molecule (EpCAM) detection. Biosensors and Bioelectronics, 93, 182-188 is available at https://doi.org/10.1016/j.bios.2016.09.012en_US
dc.subjectGraphene quantum dots (GQDs)en_US
dc.subjectMolybdenum disulfide (MoS2)en_US
dc.subjectFluorescence resonance energy transfer (FRET)en_US
dc.subjectEpithelial cell adhesion molecule (EpCAM)en_US
dc.titleA fluorescence turn-on biosensor based on graphene quantum dots (GQDs) and molybdenum disulfide (MoS2) nanosheets for epithelial cell adhesion molecule (EpCAM) detectionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage182en_US
dc.identifier.epage188en_US
dc.identifier.volume93en_US
dc.identifier.doi10.1016/j.bios.2016.09.012en_US
dcterms.abstractThis paper presents a "turn-on" fluorescence biosensor based on graphene quantum dots (GQDs) and molybdenum disulfide (MoS2) nanosheets for rapid and sensitive detection of epithelial cell adhesion molecule (EpCAM). PEGylated GQDs were used as donor molecules, which could not only largely increase emission intensity but also prevent non-specific adsorption of PEGylated GQD on MoS2 surface. The sensing platform was realized by adsorption of PEGylated GQD labelled EpCAM aptamer onto MoS2 surface via van der Waals force. The fluorescence signal of GQD was then quenched by MoS2 nanosheets via fluorescence resonance energy transfer (FRET) mechanism. In the presence of EpCAM protein, the stronger specific affinity interaction between aptamer and EpCAM protein could detach GQD labelled EpCAM aptamer from MoS2 nanosheets, leading to the restoration of fluorescence intensity. By monitoring the change of fluorescence signal, the target EpCAM protein could be detected sensitively and selectively with a linear detection range from 3 nM to 54 nM and limit of detection (LOD) around 450 pM. In addition, this nanobiosensor has been successfully used for EpCAM-expressed breast cancer MCF-7 cell detection.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBiosensors and bioelectronics, 15 July 2017, v. 93, p. 182-188en_US
dcterms.isPartOfBiosensors and bioelectronicsen_US
dcterms.issued2017-07-15-
dc.identifier.isiWOS:000399259000026-
dc.identifier.pmid27614683-
dc.identifier.ros2016000397-
dc.identifier.eissn1873-4235en_US
dc.identifier.rosgroupid2016000396-
dc.description.ros2016-2017 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validatebcrcen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberBME-0197-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHong Kong Research Granst Council; Hong Kong PhD Fellowship Scheme Fund; Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6694676-
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