Development of Label-Free Colorimetric Assay for MERS-CoV Using Gold Nanoparticles
Author(s) -
Hanbi Kim,
Minseon Park,
Joonki Hwang,
Jin Hwa Kim,
Doo Ryeon Chung,
KyuSung Lee,
Minhee Kang
Publication year - 2019
Publication title -
acs sensors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.055
H-Index - 57
ISSN - 2379-3694
DOI - 10.1021/acssensors.9b00175
Subject(s) - colloidal gold , surface plasmon resonance , absorbance , chemistry , nanoparticle , middle east respiratory syndrome coronavirus , naked eye , nanotechnology , molecule , fluorescence , biophysics , combinatorial chemistry , detection limit , materials science , covid-19 , chromatography , infectious disease (medical specialty) , biology , optics , medicine , physics , disease , pathology , organic chemistry
Worldwide outbreaks of infectious diseases necessitate the development of rapid and accurate diagnostic methods. Colorimetric assays are a representative tool to simply identify the target molecules in specimens through color changes of an indicator (e.g., nanosized metallic particle, and dye molecules). The detection method is used to confirm the presence of biomarkers visually and measure absorbance of the colored compounds at a specific wavelength. In this study, we propose a colorimetric assay based on an extended form of double-stranded DNA (dsDNA) self-assembly shielded gold nanoparticles (AuNPs) under positive electrolyte (e.g., 0.1 M MgCl 2 ) for detection of Middle East respiratory syndrome coronavirus (MERS-CoV). This platform is able to verify the existence of viral molecules through a localized surface plasmon resonance (LSPR) shift and color changes of AuNPs in the UV-vis wavelength range. We designed a pair of thiol-modified probes at either the 5' end or 3' end to organize complementary base pairs with upstream of the E protein gene (upE) and open reading frames (ORF) 1a on MERS-CoV. The dsDNA of the target and probes forms a disulfide-induced long self-assembled complex, which protects AuNPs from salt-induced aggregation and transition of optical properties. This colorimetric assay could discriminate down to 1 pmol/μL of 30 bp MERS-CoV and further be adapted for convenient on-site detection of other infectious diseases, especially in resource-limited settings.
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