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Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics

Here, we firstly introduce a detection system consisting of upconversion nanoparticles (UCNPs) and Au nanorods (AuNRs) for an ultrasensitive, rapid, quantitative and on-site detection of SARS-CoV-2 spike (S) protein based on Förster resonance energy transfer (FRET) effect. Briefly, the UCNPs capture...

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Autores principales: Li, Lihua, Song, Menglin, Lao, Xinyue, Pang, Sin-Yi, Liu, Yuan, Wong, Man-Chung, Ma, Yingjin, Yang, Mo, Hao, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575549/
https://www.ncbi.nlm.nih.gov/pubmed/36275835
http://dx.doi.org/10.1016/j.matdes.2022.111263
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author Li, Lihua
Song, Menglin
Lao, Xinyue
Pang, Sin-Yi
Liu, Yuan
Wong, Man-Chung
Ma, Yingjin
Yang, Mo
Hao, Jianhua
author_facet Li, Lihua
Song, Menglin
Lao, Xinyue
Pang, Sin-Yi
Liu, Yuan
Wong, Man-Chung
Ma, Yingjin
Yang, Mo
Hao, Jianhua
author_sort Li, Lihua
collection PubMed
description Here, we firstly introduce a detection system consisting of upconversion nanoparticles (UCNPs) and Au nanorods (AuNRs) for an ultrasensitive, rapid, quantitative and on-site detection of SARS-CoV-2 spike (S) protein based on Förster resonance energy transfer (FRET) effect. Briefly, the UCNPs capture the S protein of lysed SARS-CoV-2 in the swabs and subsequently they are bound with the anti-S antibodies modified AuNRs, resulting in significant nonradiative transitions from UCNPs (donors) to AuNRs (acceptors) at 480 nm and 800 nm, respectively. Notably, the specific recognition and quantitation of S protein can be realized in minutes at 800 nm because of the low autofluorescence and high Yb-Tm energy transfer in upconversion process. Inspiringly, the limit of detection (LOD) of the S protein can reach down to 1.06 fg mL(−1), while the recognition of nucleocapsid protein is also comparable with a commercial test kit in a shorter time (only 5 min). The established strategy is technically superior to those reported point-of-care biosensors in terms of detection time, cost, and sensitivity, which paves a new avenue for future on-site rapid viral screening and point-of-care diagnostics.
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spelling pubmed-95755492022-10-17 Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics Li, Lihua Song, Menglin Lao, Xinyue Pang, Sin-Yi Liu, Yuan Wong, Man-Chung Ma, Yingjin Yang, Mo Hao, Jianhua Mater Des Article Here, we firstly introduce a detection system consisting of upconversion nanoparticles (UCNPs) and Au nanorods (AuNRs) for an ultrasensitive, rapid, quantitative and on-site detection of SARS-CoV-2 spike (S) protein based on Förster resonance energy transfer (FRET) effect. Briefly, the UCNPs capture the S protein of lysed SARS-CoV-2 in the swabs and subsequently they are bound with the anti-S antibodies modified AuNRs, resulting in significant nonradiative transitions from UCNPs (donors) to AuNRs (acceptors) at 480 nm and 800 nm, respectively. Notably, the specific recognition and quantitation of S protein can be realized in minutes at 800 nm because of the low autofluorescence and high Yb-Tm energy transfer in upconversion process. Inspiringly, the limit of detection (LOD) of the S protein can reach down to 1.06 fg mL(−1), while the recognition of nucleocapsid protein is also comparable with a commercial test kit in a shorter time (only 5 min). The established strategy is technically superior to those reported point-of-care biosensors in terms of detection time, cost, and sensitivity, which paves a new avenue for future on-site rapid viral screening and point-of-care diagnostics. The Author(s). Published by Elsevier Ltd. 2022-11 2022-10-17 /pmc/articles/PMC9575549/ /pubmed/36275835 http://dx.doi.org/10.1016/j.matdes.2022.111263 Text en © 2022 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights 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 free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Li, Lihua
Song, Menglin
Lao, Xinyue
Pang, Sin-Yi
Liu, Yuan
Wong, Man-Chung
Ma, Yingjin
Yang, Mo
Hao, Jianhua
Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics
title Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics
title_full Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics
title_fullStr Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics
title_full_unstemmed Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics
title_short Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics
title_sort rapid and ultrasensitive detection of sars-cov-2 spike protein based on upconversion luminescence biosensor for covid-19 point-of-care diagnostics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575549/
https://www.ncbi.nlm.nih.gov/pubmed/36275835
http://dx.doi.org/10.1016/j.matdes.2022.111263
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