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Cited 4 time in webofscience Cited 4 time in scopus
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Sensitive detection of dengue virus NS1 by highly stable affibody-functionalized gold nanoparticles

Authors
Bang, JinhoPark, HeesunChoi, Won IlSung, DaekyungLee, Jin HyungLee, Kuen YongKim, Sunghyun
Issue Date
Aug-2018
Publisher
ROYAL SOC CHEMISTRY
Citation
NEW JOURNAL OF CHEMISTRY, v.42, no.15, pp.12607 - 12614
Indexed
SCIE
SCOPUS
Journal Title
NEW JOURNAL OF CHEMISTRY
Volume
42
Number
15
Start Page
12607
End Page
12614
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/4682
DOI
10.1039/c8nj02244e
ISSN
1144-0546
Abstract
Infection with dengue virus (DENV) is a serious health issue that causes severe dengue fever and occasionally lethal complications, such as dengue hemorrhagic fever. Therefore, rapid and sensitive DENV detection is important to reduce morbidity and mortality. Here, we screened dengue NS1-specific affibodies and developed highly stable anti-NS1 affibody-functionalized AuNPs to improve the detection sensitivity of the NS1 antigen in ELISA. First, we screened NS1 antigen-specific affibody molecules (Z(Ns1)12, Z(Ns1)16, and Z(Ns1) 46) from an affibody phage Library. The affibodies were then expressed and purified from Escherichia coli. Among them, the Z(Ns1)12 affibody showed the highest equilibrium binding constant (K-d) of 1 mu.M and was sufficiently stable at high temperatures. This affibody was functionalized on AuNPs measuring 20 nm in diameter, which were used as carriers to achieve amplification of the signal in ELISA. The developed anti-NS1 affibody-functionalized AuNPs ((Z(Ns)12)(2) -AuNP) showed good properties, such as easy synthesis, a high number of affibody conjugations on the AuNPs, and excellent stability under harsh conditions with high salt concentrations and temperature. In addition, this nanoparticle-based enhanced ELISA resulted in a 14.2-fold signal amplification performance for dengue NS1 detection in comparison with the affibody-based ELISA. This novel and sensitive method using (Z(Ns)12)(2) -AuNPs may have applications in the detection of DENV in infected patients at an early stage and for the detection of other pathogens in clinical diagnostics.
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