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Development of Label-Free Colorimetric Assay for MERS-CoV Using Gold Nanoparticles

Identifieur interne : 000125 ( Pmc/Curation ); précédent : 000124; suivant : 000126

Development of Label-Free Colorimetric Assay for MERS-CoV Using Gold Nanoparticles

Auteurs : Hanbi Kim ; Minseon Park [Corée du Sud] ; Joonki Hwang ; Jin Hwa Kim ; Doo-Ryeon Chung [Corée du Sud] ; Kyu-Sung Lee [Corée du Sud] ; Minhee Kang [Corée du Sud]

Source :

RBID : PMC:7119221

Abstract

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 MgCl2) 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.


Url:
DOI: 10.1021/acssensors.9b00175
PubMed: 31062580
PubMed Central: 7119221

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PMC:7119221

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Doo-Ryeon Chung
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Le document en format XML

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<p>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
<sub>2</sub>
) 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.</p>
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<pmc article-type="research-article" xml:lang="EN">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">ACS Sens</journal-id>
<journal-id journal-id-type="iso-abbrev">ACS Sens</journal-id>
<journal-id journal-id-type="publisher-id">se</journal-id>
<journal-id journal-id-type="coden">ascefj</journal-id>
<journal-title-group>
<journal-title>ACS Sensors</journal-title>
</journal-title-group>
<issn pub-type="epub">2379-3694</issn>
<publisher>
<publisher-name>American Chemical Society</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">31062580</article-id>
<article-id pub-id-type="pmc">7119221</article-id>
<article-id pub-id-type="doi">10.1021/acssensors.9b00175</article-id>
<article-categories>
<subj-group>
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Development of Label-Free Colorimetric Assay for MERS-CoV Using Gold Nanoparticles</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" id="ath1">
<name>
<surname>Kim</surname>
<given-names>Hanbi</given-names>
</name>
<xref rid="aff1a" ref-type="aff"></xref>
<xref rid="notes3" ref-type="notes"></xref>
</contrib>
<contrib contrib-type="author" id="ath2">
<name>
<surname>Park</surname>
<given-names>Minseon</given-names>
</name>
<xref rid="aff1a" ref-type="aff"></xref>
<xref rid="aff2" ref-type="aff"></xref>
<xref rid="notes3" ref-type="notes"></xref>
</contrib>
<contrib contrib-type="author" id="ath3">
<name>
<surname>Hwang</surname>
<given-names>Joonki</given-names>
</name>
<xref rid="aff1a" ref-type="aff"></xref>
<xref rid="notes2" ref-type="notes"></xref>
</contrib>
<contrib contrib-type="author" id="ath4">
<name>
<surname>Kim</surname>
<given-names>Jin Hwa</given-names>
</name>
<xref rid="aff1a" ref-type="aff"></xref>
</contrib>
<contrib contrib-type="author" id="ath5">
<name>
<surname>Chung</surname>
<given-names>Doo-Ryeon</given-names>
</name>
<xref rid="aff1a" ref-type="aff">§</xref>
<xref rid="aff4" ref-type="aff"></xref>
<xref rid="aff5a" ref-type="aff"></xref>
</contrib>
<contrib contrib-type="author" corresp="yes" id="ath6">
<name>
<surname>Lee</surname>
<given-names>Kyu-sung</given-names>
</name>
<xref rid="cor1" ref-type="other">*</xref>
<xref rid="aff1a" ref-type="aff"></xref>
<xref rid="aff2" ref-type="aff"></xref>
<xref rid="aff5a" ref-type="aff">#</xref>
</contrib>
<contrib contrib-type="author" corresp="yes" id="ath7">
<name>
<surname>Kang</surname>
<given-names>Minhee</given-names>
</name>
<xref rid="cor2" ref-type="other">*</xref>
<xref rid="aff1a" ref-type="aff"></xref>
<xref rid="aff2" ref-type="aff"></xref>
</contrib>
<aff id="aff1a">
<sup></sup>
Smart Healthcare & Device Research Center and
<sup>§</sup>
Center for Infection Prevention and Control,
<institution>Samsung Medical Center</institution>
, Seoul,
<country>Korea</country>
</aff>
<aff id="aff2">
<label></label>
Department of Medical Device Management and Research, SAIHST (Samsung Advanced Institute for Health Sciences & Technology),
<institution>Sungkyunkwan University</institution>
, Seoul,
<country>Korea</country>
</aff>
<aff id="aff4">
<label></label>
<institution>Asia Pacific Foundation for Infectious Diseases (APFID)</institution>
, Seoul,
<country>Korea</country>
</aff>
<aff id="aff5a">
<sup></sup>
Division of Infectious Diseases, Department of Internal Medicine and
<sup>#</sup>
Department of Urology,
<institution>Samsung Medical Center, Sungkyunkwan University School of Medicine</institution>
, Seoul,
<country>Korea</country>
</aff>
</contrib-group>
<author-notes>
<corresp id="cor1">
<label>*</label>
E-mail:
<email>minikang@skku.edu</email>
.</corresp>
<corresp id="cor2">
<label>*</label>
E-mail:
<email>minhee.kang@samsung.com</email>
.</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>07</day>
<month>05</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="ppub">
<day>24</day>
<month>05</month>
<year>2019</year>
</pub-date>
<volume>4</volume>
<issue>5</issue>
<fpage>1306</fpage>
<lpage>1312</lpage>
<history>
<date date-type="received">
<day>23</day>
<month>01</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>07</day>
<month>05</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2019 American Chemical Society</copyright-statement>
<copyright-year>2019</copyright-year>
<copyright-holder>American Chemical Society</copyright-holder>
<license license-type="open-access">
<license-p>This article is made available via the PMC Open Access Subset for unrestricted RESEARCH re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p>
</license>
</permissions>
<abstract>
<p content-type="toc-graphic">
<graphic xlink:href="se9b00175_0005" id="ab-tgr1"></graphic>
</p>
<p>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
<sub>2</sub>
) 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.</p>
</abstract>
<kwd-group>
<kwd>colorimetric assay</kwd>
<kwd>Middle East respiratory syndrome coronavirus (MERS-CoV)</kwd>
<kwd>molecular diagnosis</kwd>
<kwd>gold nanoparticle</kwd>
<kwd>label-free detection</kwd>
</kwd-group>
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</front>
</pmc>
</record>

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