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Temperature-Responsive Liposome-Linked Immunosorbent Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes
[Image: see text] Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the etiological agent of coronavirus disease 2019 (COVID-19), has infected more than 340 million people since the outbreak of the pandemic in 2019, resulting in approximately 55 million deaths. The rapid and eff...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328125/ https://www.ncbi.nlm.nih.gov/pubmed/35915635 http://dx.doi.org/10.1021/acsomega.2c03597 |
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author | Hu, Runkai Hotta, Morihiro Maruyama, Taro Fujisawa, Mizuki Sou, Keitaro Takeoka, Shinji |
author_facet | Hu, Runkai Hotta, Morihiro Maruyama, Taro Fujisawa, Mizuki Sou, Keitaro Takeoka, Shinji |
author_sort | Hu, Runkai |
collection | PubMed |
description | [Image: see text] Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the etiological agent of coronavirus disease 2019 (COVID-19), has infected more than 340 million people since the outbreak of the pandemic in 2019, resulting in approximately 55 million deaths. The rapid and effective diagnosis of COVID-19 patients is vital to prevent the spread of the disease. In a previous study, we reported a novel temperature-responsive liposome-linked immunosorbent assay (TLip-LISA) using biotinylated-TLip that exhibited high detection sensitivity for the prostate-specific antigen. Herein, we used immunoglobulin-TLip (IgG-TLip), in which the antibodies were directly conjugated to the liposomal surface to simplify pretreatment procedures and reduce the detection time for SARS-CoV-2. The results indicated that TLip-LISA could detect the recombinant nucleocapsid protein and the nucleocapsid protein in inactivated virus with 20 min incubation time in total, and the limit of detection was calculated to be 2.2 and 1.0 pg/mL, respectively. Therefore, TLip-LISA has high potential to be used in clinic for rapid diagnosis and disease control. |
format | Online Article Text |
id | pubmed-9328125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93281252022-07-28 Temperature-Responsive Liposome-Linked Immunosorbent Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes Hu, Runkai Hotta, Morihiro Maruyama, Taro Fujisawa, Mizuki Sou, Keitaro Takeoka, Shinji ACS Omega [Image: see text] Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the etiological agent of coronavirus disease 2019 (COVID-19), has infected more than 340 million people since the outbreak of the pandemic in 2019, resulting in approximately 55 million deaths. The rapid and effective diagnosis of COVID-19 patients is vital to prevent the spread of the disease. In a previous study, we reported a novel temperature-responsive liposome-linked immunosorbent assay (TLip-LISA) using biotinylated-TLip that exhibited high detection sensitivity for the prostate-specific antigen. Herein, we used immunoglobulin-TLip (IgG-TLip), in which the antibodies were directly conjugated to the liposomal surface to simplify pretreatment procedures and reduce the detection time for SARS-CoV-2. The results indicated that TLip-LISA could detect the recombinant nucleocapsid protein and the nucleocapsid protein in inactivated virus with 20 min incubation time in total, and the limit of detection was calculated to be 2.2 and 1.0 pg/mL, respectively. Therefore, TLip-LISA has high potential to be used in clinic for rapid diagnosis and disease control. American Chemical Society 2022-07-21 /pmc/articles/PMC9328125/ /pubmed/35915635 http://dx.doi.org/10.1021/acsomega.2c03597 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Hu, Runkai Hotta, Morihiro Maruyama, Taro Fujisawa, Mizuki Sou, Keitaro Takeoka, Shinji Temperature-Responsive Liposome-Linked Immunosorbent Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes |
title | Temperature-Responsive
Liposome-Linked Immunosorbent
Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes |
title_full | Temperature-Responsive
Liposome-Linked Immunosorbent
Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes |
title_fullStr | Temperature-Responsive
Liposome-Linked Immunosorbent
Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes |
title_full_unstemmed | Temperature-Responsive
Liposome-Linked Immunosorbent
Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes |
title_short | Temperature-Responsive
Liposome-Linked Immunosorbent
Assay for the Rapid Detection of SARS-CoV-2 Using Immunoliposomes |
title_sort | temperature-responsive
liposome-linked immunosorbent
assay for the rapid detection of sars-cov-2 using immunoliposomes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328125/ https://www.ncbi.nlm.nih.gov/pubmed/35915635 http://dx.doi.org/10.1021/acsomega.2c03597 |
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