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A novel thermostable beetle luciferase based cytotoxicity assay
Cytotoxicity assays are essential for the testing and development of novel immunotherapies for the treatment of cancer. We recently described a novel cytotoxicity assay, termed the Matador assay, which was based on marine luciferases and their engineered derivatives. In this study, we describe the d...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113442/ https://www.ncbi.nlm.nih.gov/pubmed/33976304 http://dx.doi.org/10.1038/s41598-021-89404-z |
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author | Choi, Sunju Matta, Hittu Gopalakrishnan, Ramakrishnan Natarajan, Venkatesh Gong, Songjie Jeronimo, Alberto Kuo, Wei-Ying Bravo, Bryant Chaudhary, Preet M. |
author_facet | Choi, Sunju Matta, Hittu Gopalakrishnan, Ramakrishnan Natarajan, Venkatesh Gong, Songjie Jeronimo, Alberto Kuo, Wei-Ying Bravo, Bryant Chaudhary, Preet M. |
author_sort | Choi, Sunju |
collection | PubMed |
description | Cytotoxicity assays are essential for the testing and development of novel immunotherapies for the treatment of cancer. We recently described a novel cytotoxicity assay, termed the Matador assay, which was based on marine luciferases and their engineered derivatives. In this study, we describe the development of a new cytotoxicity assay termed ‘Matador-Glo assay’ which takes advantage of a thermostable variant of Click Beetle Luciferase (Luc146-1H2). Matador-Glo assay utilizes Luc146-1H2 and D-luciferin as the luciferase-substrate pair for luminescence detection. The assay involves ectopic over-expression of Luc146-1H2 in the cytosol of target cells of interest. Upon damage to the membrane integrity, the Luc146-1H2 is either released from the dead and dying cells or its activity is preferentially measured in dead and dying cells. We demonstrate that this assay is simple, fast, specific, sensitive, cost-efficient, and not labor-intensive. We further demonstrate that the Matador-Glo assay can be combined with the marine luciferase-based Matador assay to develop a dual luciferase assay for cell death detection. Finally, we demonstrate that the Luc146-1H2 expressing target cells can also be used for in vivo bioluminescence imaging applications. |
format | Online Article Text |
id | pubmed-8113442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81134422021-05-12 A novel thermostable beetle luciferase based cytotoxicity assay Choi, Sunju Matta, Hittu Gopalakrishnan, Ramakrishnan Natarajan, Venkatesh Gong, Songjie Jeronimo, Alberto Kuo, Wei-Ying Bravo, Bryant Chaudhary, Preet M. Sci Rep Article Cytotoxicity assays are essential for the testing and development of novel immunotherapies for the treatment of cancer. We recently described a novel cytotoxicity assay, termed the Matador assay, which was based on marine luciferases and their engineered derivatives. In this study, we describe the development of a new cytotoxicity assay termed ‘Matador-Glo assay’ which takes advantage of a thermostable variant of Click Beetle Luciferase (Luc146-1H2). Matador-Glo assay utilizes Luc146-1H2 and D-luciferin as the luciferase-substrate pair for luminescence detection. The assay involves ectopic over-expression of Luc146-1H2 in the cytosol of target cells of interest. Upon damage to the membrane integrity, the Luc146-1H2 is either released from the dead and dying cells or its activity is preferentially measured in dead and dying cells. We demonstrate that this assay is simple, fast, specific, sensitive, cost-efficient, and not labor-intensive. We further demonstrate that the Matador-Glo assay can be combined with the marine luciferase-based Matador assay to develop a dual luciferase assay for cell death detection. Finally, we demonstrate that the Luc146-1H2 expressing target cells can also be used for in vivo bioluminescence imaging applications. Nature Publishing Group UK 2021-05-11 /pmc/articles/PMC8113442/ /pubmed/33976304 http://dx.doi.org/10.1038/s41598-021-89404-z Text en © The Author(s) 2021 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 Choi, Sunju Matta, Hittu Gopalakrishnan, Ramakrishnan Natarajan, Venkatesh Gong, Songjie Jeronimo, Alberto Kuo, Wei-Ying Bravo, Bryant Chaudhary, Preet M. A novel thermostable beetle luciferase based cytotoxicity assay |
title | A novel thermostable beetle luciferase based cytotoxicity assay |
title_full | A novel thermostable beetle luciferase based cytotoxicity assay |
title_fullStr | A novel thermostable beetle luciferase based cytotoxicity assay |
title_full_unstemmed | A novel thermostable beetle luciferase based cytotoxicity assay |
title_short | A novel thermostable beetle luciferase based cytotoxicity assay |
title_sort | novel thermostable beetle luciferase based cytotoxicity assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113442/ https://www.ncbi.nlm.nih.gov/pubmed/33976304 http://dx.doi.org/10.1038/s41598-021-89404-z |
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