Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.analchem.7b00066
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dc.titleExploiting the Anti-Aggregation of Gold Nanostars for Rapid Detection of Hand, Foot, and Mouth Disease Causing Enterovirus 71 Using Surface-Enhanced Raman Spectroscopy
dc.contributor.authorReyes, Miguel
dc.contributor.authorPiotrowski, Marek
dc.contributor.authorAng, Swee Kim
dc.contributor.authorChan, Jingqi
dc.contributor.authorHe, Shuai
dc.contributor.authorChu, Justin Jang Hann
dc.contributor.authorKah, James Chen Yong
dc.date.accessioned2020-08-21T06:06:23Z
dc.date.available2020-08-21T06:06:23Z
dc.date.issued2017-05-16
dc.identifier.citationReyes, Miguel, Piotrowski, Marek, Ang, Swee Kim, Chan, Jingqi, He, Shuai, Chu, Justin Jang Hann, Kah, James Chen Yong (2017-05-16). Exploiting the Anti-Aggregation of Gold Nanostars for Rapid Detection of Hand, Foot, and Mouth Disease Causing Enterovirus 71 Using Surface-Enhanced Raman Spectroscopy. ANALYTICAL CHEMISTRY 89 (10) : 5373-5381. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.analchem.7b00066
dc.identifier.issn00032700
dc.identifier.issn15206882
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/173280
dc.description.abstract© 2017 American Chemical Society. Enterovirus 71 (EV71) is a major public health threat that requires rapid point-of-care detection. Here, we developed a surface-enhanced Raman spectroscopy (SERS)-based scheme that utilized protein-induced aggregation of colloidal gold nanostars (AuNS) to rapidly detect EV71 without the need for fabricating a solid substrate, Raman labels or complicated sample handling. We used AuNS (hydrodynamic diameter, DH of 105.12 ± 1.13 nm) conjugated to recombinant scavenger receptor class B, member 2 (SCARB2) protein with known affinity to EV71. In the absence of EV71, AuNS-SCARB2 aggregated in biological media and produced four enhanced Raman peaks at 390, 510, 670, and 910 cm-1. In the presence of EV71, the three peaks at 510, 670, and 910 cm-1 disappeared, while the peak at 390 cm-1 diminished in intensity as the virus bound to AuNS-SCARB2 and prevented them from aggregation. These three peaks (510, 670, and 910 cm-1) were potential markers for specific detection of EV71 as their disappearance was not observable with a different dengue virus (DENV) as our control. Furthermore, the Raman measurements from colloidal SERS were more sensitive in probing the aggregation of AuNS-SCARB2 for detecting the presence of EV71 in protein-rich samples compared to UV-vis spectrum measurements. With this facile "anti-aggregation" approach, we were able to detect EV71 in protein-rich biological medium within 15 min with reasonable sensitivity of 107 pfu/mL and minimal sample preparation, making this translatable for point-of-care applications.
dc.language.isoen
dc.publisherAMER CHEMICAL SOC
dc.sourceElements
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectChemistry, Analytical
dc.subjectChemistry
dc.subjectNANOPARTICLE AGGREGATION
dc.subjectSCATTERING SERS
dc.subjectPROTEIN CORONA
dc.subjectSILVER
dc.subjectIMMUNOASSAY
dc.subjectEV71
dc.subjectEPIDEMIOLOGY
dc.subjectSTABILITY
dc.subjectMOLECULES
dc.subjectSUBSTRATE
dc.typeArticle
dc.date.updated2020-06-23T08:00:08Z
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1021/acs.analchem.7b00066
dc.description.sourcetitleANALYTICAL CHEMISTRY
dc.description.volume89
dc.description.issue10
dc.description.page5373-5381
dc.published.statePublished
dc.description.redepositCompleted
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