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A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection
Proteases play critical roles in various biological processes, including apoptosis and viral infection. Several protease biosensors have been developed; however, obtaining a reliable signal from a very low level of endogenous protease activity remains a challenge. In this study, we developed a highl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887574/ https://www.ncbi.nlm.nih.gov/pubmed/36720982 http://dx.doi.org/10.1038/s41598-023-28984-4 |
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author | Arakawa, Masashi Yoshida, Akiho Okamura, Shinya Ebina, Hirotaka Morita, Eiji |
author_facet | Arakawa, Masashi Yoshida, Akiho Okamura, Shinya Ebina, Hirotaka Morita, Eiji |
author_sort | Arakawa, Masashi |
collection | PubMed |
description | Proteases play critical roles in various biological processes, including apoptosis and viral infection. Several protease biosensors have been developed; however, obtaining a reliable signal from a very low level of endogenous protease activity remains a challenge. In this study, we developed a highly sensitive protease biosensor, named FlipNanoLuc, based on the Oplophorus gracilirostris NanoLuc luciferase. The flipped β-strand was restored by protease activation and cleavage, resulting in the reconstitution of luciferase and enzymatic activity. By making several modifications, such as introducing NanoBiT technology and CL1-PEST1 degradation tag, the FlipNanoLuc-based protease biosensor system achieved more than 500-fold luminescence increase in the corresponding protease-overexpressing cells. We demonstrated that the FlipNanoLuc-based caspase sensor can be utilized for the detection of staurosporine-induced apoptosis with sixfold increase in luminescence. Furthermore, we also demonstrated that the FlipNanoLuc-based coronavirus 3CL-protease sensor can be used to detect human coronavirus OC43 with tenfold increase in luminescence and severe acute respiratory syndrome-coronavirus-2 infections with 20-fold increase in luminescence by introducing the stem-loop 1 sequence to prevent the virus inducing global translational shutdown. |
format | Online Article Text |
id | pubmed-9887574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98875742023-01-31 A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection Arakawa, Masashi Yoshida, Akiho Okamura, Shinya Ebina, Hirotaka Morita, Eiji Sci Rep Article Proteases play critical roles in various biological processes, including apoptosis and viral infection. Several protease biosensors have been developed; however, obtaining a reliable signal from a very low level of endogenous protease activity remains a challenge. In this study, we developed a highly sensitive protease biosensor, named FlipNanoLuc, based on the Oplophorus gracilirostris NanoLuc luciferase. The flipped β-strand was restored by protease activation and cleavage, resulting in the reconstitution of luciferase and enzymatic activity. By making several modifications, such as introducing NanoBiT technology and CL1-PEST1 degradation tag, the FlipNanoLuc-based protease biosensor system achieved more than 500-fold luminescence increase in the corresponding protease-overexpressing cells. We demonstrated that the FlipNanoLuc-based caspase sensor can be utilized for the detection of staurosporine-induced apoptosis with sixfold increase in luminescence. Furthermore, we also demonstrated that the FlipNanoLuc-based coronavirus 3CL-protease sensor can be used to detect human coronavirus OC43 with tenfold increase in luminescence and severe acute respiratory syndrome-coronavirus-2 infections with 20-fold increase in luminescence by introducing the stem-loop 1 sequence to prevent the virus inducing global translational shutdown. Nature Publishing Group UK 2023-01-31 /pmc/articles/PMC9887574/ /pubmed/36720982 http://dx.doi.org/10.1038/s41598-023-28984-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Arakawa, Masashi Yoshida, Akiho Okamura, Shinya Ebina, Hirotaka Morita, Eiji A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection |
title | A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection |
title_full | A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection |
title_fullStr | A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection |
title_full_unstemmed | A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection |
title_short | A highly sensitive NanoLuc-based protease biosensor for detecting apoptosis and SARS-CoV-2 infection |
title_sort | highly sensitive nanoluc-based protease biosensor for detecting apoptosis and sars-cov-2 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887574/ https://www.ncbi.nlm.nih.gov/pubmed/36720982 http://dx.doi.org/10.1038/s41598-023-28984-4 |
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