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https://doi.org/10.1021/acs.analchem.7b00066
Title: | Exploiting the Anti-Aggregation of Gold Nanostars for Rapid Detection of Hand, Foot, and Mouth Disease Causing Enterovirus 71 Using Surface-Enhanced Raman Spectroscopy | Authors: | Reyes, Miguel Piotrowski, Marek Ang, Swee Kim Chan, Jingqi He, Shuai Chu, Justin Jang Hann Kah, James Chen Yong |
Keywords: | Science & Technology Physical Sciences Chemistry, Analytical Chemistry NANOPARTICLE AGGREGATION SCATTERING SERS PROTEIN CORONA SILVER IMMUNOASSAY EV71 EPIDEMIOLOGY STABILITY MOLECULES SUBSTRATE |
Issue Date: | 16-May-2017 | Publisher: | AMER CHEMICAL SOC | Citation: | Reyes, 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 | 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. | Source Title: | ANALYTICAL CHEMISTRY | URI: | https://scholarbank.nus.edu.sg/handle/10635/173280 | ISSN: | 00032700 15206882 |
DOI: | 10.1021/acs.analchem.7b00066 |
Appears in Collections: | Staff Publications Elements |
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