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A simeprevir-inducible molecular switch for the control of cell and gene therapies
Chemical inducer of dimerization (CID) modules can be used effectively as molecular switches to control biological processes, and thus there is significant interest within the synthetic biology community in identifying novel CID systems. To date, CID modules have been used primarily in engineering c...
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/PMC10682029/ https://www.ncbi.nlm.nih.gov/pubmed/38012128 http://dx.doi.org/10.1038/s41467-023-43484-9 |
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author | Chin, Stacey E. Schindler, Christina Vinall, Lisa Dodd, Roger B. Bamber, Lisa Legg, Sandrine Sigurdardottir, Anna Rees, D. Gareth Malcolm, Tim I. M. Spratley, Samantha J. Granéli, Cecilia Sumner, Jonathan Tigue, Natalie J. |
author_facet | Chin, Stacey E. Schindler, Christina Vinall, Lisa Dodd, Roger B. Bamber, Lisa Legg, Sandrine Sigurdardottir, Anna Rees, D. Gareth Malcolm, Tim I. M. Spratley, Samantha J. Granéli, Cecilia Sumner, Jonathan Tigue, Natalie J. |
author_sort | Chin, Stacey E. |
collection | PubMed |
description | Chemical inducer of dimerization (CID) modules can be used effectively as molecular switches to control biological processes, and thus there is significant interest within the synthetic biology community in identifying novel CID systems. To date, CID modules have been used primarily in engineering cells for in vitro applications. To broaden their utility to the clinical setting, including the potential to control cell and gene therapies, the identification of novel CID modules should consider factors such as the safety and pharmacokinetic profile of the small molecule inducer, and the orthogonality and immunogenicity of the protein components. Here we describe a CID module based on the orally available, approved, small molecule simeprevir and its target, the NS3/4A protease from hepatitis C virus. We demonstrate the utility of this CID module as a molecular switch to control biological processes such as gene expression and apoptosis in vitro, and show that the CID system can be used to rapidly induce apoptosis in tumor cells in a xenograft mouse model, leading to complete tumor regression. |
format | Online Article Text |
id | pubmed-10682029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106820292023-11-30 A simeprevir-inducible molecular switch for the control of cell and gene therapies Chin, Stacey E. Schindler, Christina Vinall, Lisa Dodd, Roger B. Bamber, Lisa Legg, Sandrine Sigurdardottir, Anna Rees, D. Gareth Malcolm, Tim I. M. Spratley, Samantha J. Granéli, Cecilia Sumner, Jonathan Tigue, Natalie J. Nat Commun Article Chemical inducer of dimerization (CID) modules can be used effectively as molecular switches to control biological processes, and thus there is significant interest within the synthetic biology community in identifying novel CID systems. To date, CID modules have been used primarily in engineering cells for in vitro applications. To broaden their utility to the clinical setting, including the potential to control cell and gene therapies, the identification of novel CID modules should consider factors such as the safety and pharmacokinetic profile of the small molecule inducer, and the orthogonality and immunogenicity of the protein components. Here we describe a CID module based on the orally available, approved, small molecule simeprevir and its target, the NS3/4A protease from hepatitis C virus. We demonstrate the utility of this CID module as a molecular switch to control biological processes such as gene expression and apoptosis in vitro, and show that the CID system can be used to rapidly induce apoptosis in tumor cells in a xenograft mouse model, leading to complete tumor regression. Nature Publishing Group UK 2023-11-27 /pmc/articles/PMC10682029/ /pubmed/38012128 http://dx.doi.org/10.1038/s41467-023-43484-9 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chin, Stacey E. Schindler, Christina Vinall, Lisa Dodd, Roger B. Bamber, Lisa Legg, Sandrine Sigurdardottir, Anna Rees, D. Gareth Malcolm, Tim I. M. Spratley, Samantha J. Granéli, Cecilia Sumner, Jonathan Tigue, Natalie J. A simeprevir-inducible molecular switch for the control of cell and gene therapies |
title | A simeprevir-inducible molecular switch for the control of cell and gene therapies |
title_full | A simeprevir-inducible molecular switch for the control of cell and gene therapies |
title_fullStr | A simeprevir-inducible molecular switch for the control of cell and gene therapies |
title_full_unstemmed | A simeprevir-inducible molecular switch for the control of cell and gene therapies |
title_short | A simeprevir-inducible molecular switch for the control of cell and gene therapies |
title_sort | simeprevir-inducible molecular switch for the control of cell and gene therapies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682029/ https://www.ncbi.nlm.nih.gov/pubmed/38012128 http://dx.doi.org/10.1038/s41467-023-43484-9 |
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