Thermoplasmonic-Assisted Cyclic Cleavage Amplification for Self-Validating Plasmonic Detection of SARS-CoV-2
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Date
2021-04-27
Publication Type
Journal Article
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yes
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Abstract
The coronavirus disease 2019 (COVID-19) has penetrated every populated patch of the globe and sows destruction in our daily life. Reliable and sensitive virus sensing systems are therefore of vital importance for timely infection detection and transmission prevention. Here we present a thermoplasmonic-assisted dual-mode transducing (TP-DMT) concept, where an amplification-free-based direct viral RNA detection and an amplification-based cyclic fluorescence probe cleavage (CFPC) detection collaborated to provide a sensitive and self-validating plasmonic nanoplatform for quantifying trace amounts of SARS-CoV-2 within 30 min. In the CFPC detection, endonuclease IV recognized the synthetic abasic site and cleaved the fluorescent probes in the hybridized duplex. The nanoscale thermoplasmonic heating dehybridized the shortened fluorescent probes and facilitated the cyclical binding–cleavage–dissociation (BCD) process, which could deliver a highly sensitive amplification-based response. This TP-DMT approach was successfully validated by testing clinical COVID-19 patient samples, which indicated its potential applications in fast clinical infection screening and real-time environmental monitoring.
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published
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Book title
Journal / series
Volume
15 (4)
Pages / Article No.
7536 - 7546
Publisher
American Chemical Society
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Date collected
Date created
Subject
Thermoplasmonics; SARS-CoV-2; COVID-19; Plasmonics; Biosensor; Cyclic cleavage amplification
Organisational unit
03887 - Wang, Jing / Wang, Jing
Notes
Funding
198258 - Development of a real-time biosensing system of SARS-CoV-2 to improve healthcare workers safety during COVID 19 pandemics (SNF)