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Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein
The COVID-19 pandemic has demonstrated the need for exploring different diagnostic and therapeutic modalities to tackle future viral threats. In this vein, we propose the idea of sentinel cells, cellular biosensors capable of detecting viral antigens and responding to them with customizable response...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077567/ https://www.ncbi.nlm.nih.gov/pubmed/33907743 http://dx.doi.org/10.1101/2021.04.20.440678 |
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author | Weinberg, Zara Y. Hilburger, Claire E. Kim, Matthew Cao, Longxing Khalid, Mir Elmes, Sarah Diwanji, Devan Hernandez, Evelyn Lopez, Jocelyne Schaefer, Kaitlin Smith, Amber M. Zhou, Fengbo Kumar, G. Renuka Ott, Melanie Baker, David El-Samad, Hana |
author_facet | Weinberg, Zara Y. Hilburger, Claire E. Kim, Matthew Cao, Longxing Khalid, Mir Elmes, Sarah Diwanji, Devan Hernandez, Evelyn Lopez, Jocelyne Schaefer, Kaitlin Smith, Amber M. Zhou, Fengbo Kumar, G. Renuka Ott, Melanie Baker, David El-Samad, Hana |
author_sort | Weinberg, Zara Y. |
collection | PubMed |
description | The COVID-19 pandemic has demonstrated the need for exploring different diagnostic and therapeutic modalities to tackle future viral threats. In this vein, we propose the idea of sentinel cells, cellular biosensors capable of detecting viral antigens and responding to them with customizable responses. Using SARS-CoV-2 as a test case, we developed a live cell sensor (SARSNotch) using a de novo-designed protein binder against the SARS-CoV-2 Spike protein. SARSNotch is capable of driving custom genetically-encoded payloads in immortalized cell lines or in primary T lymphocytes in response to purified SARS-CoV-2 Spike or in the presence of Spike-expressing cells. Furthermore, SARSNotch is functional in a cellular system used in directed evolution platforms for development of better binders or therapeutics. In keeping with the rapid dissemination of scientific knowledge that has characterized the incredible scientific response to the ongoing pandemic, we extend an open invitation for others to make use of and improve SARSNotch sentinel cells in the hopes of unlocking the potential of the next generation of smart antiviral therapeutics. |
format | Online Article Text |
id | pubmed-8077567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-80775672021-04-28 Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein Weinberg, Zara Y. Hilburger, Claire E. Kim, Matthew Cao, Longxing Khalid, Mir Elmes, Sarah Diwanji, Devan Hernandez, Evelyn Lopez, Jocelyne Schaefer, Kaitlin Smith, Amber M. Zhou, Fengbo Kumar, G. Renuka Ott, Melanie Baker, David El-Samad, Hana bioRxiv Article The COVID-19 pandemic has demonstrated the need for exploring different diagnostic and therapeutic modalities to tackle future viral threats. In this vein, we propose the idea of sentinel cells, cellular biosensors capable of detecting viral antigens and responding to them with customizable responses. Using SARS-CoV-2 as a test case, we developed a live cell sensor (SARSNotch) using a de novo-designed protein binder against the SARS-CoV-2 Spike protein. SARSNotch is capable of driving custom genetically-encoded payloads in immortalized cell lines or in primary T lymphocytes in response to purified SARS-CoV-2 Spike or in the presence of Spike-expressing cells. Furthermore, SARSNotch is functional in a cellular system used in directed evolution platforms for development of better binders or therapeutics. In keeping with the rapid dissemination of scientific knowledge that has characterized the incredible scientific response to the ongoing pandemic, we extend an open invitation for others to make use of and improve SARSNotch sentinel cells in the hopes of unlocking the potential of the next generation of smart antiviral therapeutics. Cold Spring Harbor Laboratory 2021-04-20 /pmc/articles/PMC8077567/ /pubmed/33907743 http://dx.doi.org/10.1101/2021.04.20.440678 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Weinberg, Zara Y. Hilburger, Claire E. Kim, Matthew Cao, Longxing Khalid, Mir Elmes, Sarah Diwanji, Devan Hernandez, Evelyn Lopez, Jocelyne Schaefer, Kaitlin Smith, Amber M. Zhou, Fengbo Kumar, G. Renuka Ott, Melanie Baker, David El-Samad, Hana Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein |
title | Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein |
title_full | Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein |
title_fullStr | Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein |
title_full_unstemmed | Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein |
title_short | Sentinel cells enable genetic detection of SARS-CoV-2 Spike protein |
title_sort | sentinel cells enable genetic detection of sars-cov-2 spike protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077567/ https://www.ncbi.nlm.nih.gov/pubmed/33907743 http://dx.doi.org/10.1101/2021.04.20.440678 |
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