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Optically activated, customizable, excitable cells
Genetically encoded fluorescent biosensors are powerful tools for studying complex signaling in the nervous system, and now both Ca(2+) and voltage sensors are available to study the signaling behavior of entire neural circuits. There is a pressing need for improved sensors, but improving them is ch...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773186/ https://www.ncbi.nlm.nih.gov/pubmed/33378334 http://dx.doi.org/10.1371/journal.pone.0229051 |
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author | Thomas, Merrilee Hughes, Thomas E. |
author_facet | Thomas, Merrilee Hughes, Thomas E. |
author_sort | Thomas, Merrilee |
collection | PubMed |
description | Genetically encoded fluorescent biosensors are powerful tools for studying complex signaling in the nervous system, and now both Ca(2+) and voltage sensors are available to study the signaling behavior of entire neural circuits. There is a pressing need for improved sensors, but improving them is challenging because testing them involves a low throughput, labor-intensive processes. Our goal was to create synthetic, excitable cells that can be activated with brief pulses of blue light and serve as a medium throughput platform for screening the next generation of sensors. In this live cell system, blue light activates an adenylyl cyclase enzyme (bPAC) that increases intracellular cAMP (Stierl M et al. 2011). In turn, the cAMP opens a cAMP-gated ion channel. This produces slow, whole-cell Ca(2+) transients and voltage changes. To increase the speed of these transients, we add the inwardly rectifying potassium channel Kir2.1, the bacterial voltage-gated sodium channel NAVROSD, and Connexin-43. The result is a highly reproducible, medium-throughput, live cell system that can be used to screen voltage and Ca(2+) sensors. |
format | Online Article Text |
id | pubmed-7773186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77731862021-01-08 Optically activated, customizable, excitable cells Thomas, Merrilee Hughes, Thomas E. PLoS One Research Article Genetically encoded fluorescent biosensors are powerful tools for studying complex signaling in the nervous system, and now both Ca(2+) and voltage sensors are available to study the signaling behavior of entire neural circuits. There is a pressing need for improved sensors, but improving them is challenging because testing them involves a low throughput, labor-intensive processes. Our goal was to create synthetic, excitable cells that can be activated with brief pulses of blue light and serve as a medium throughput platform for screening the next generation of sensors. In this live cell system, blue light activates an adenylyl cyclase enzyme (bPAC) that increases intracellular cAMP (Stierl M et al. 2011). In turn, the cAMP opens a cAMP-gated ion channel. This produces slow, whole-cell Ca(2+) transients and voltage changes. To increase the speed of these transients, we add the inwardly rectifying potassium channel Kir2.1, the bacterial voltage-gated sodium channel NAVROSD, and Connexin-43. The result is a highly reproducible, medium-throughput, live cell system that can be used to screen voltage and Ca(2+) sensors. Public Library of Science 2020-12-30 /pmc/articles/PMC7773186/ /pubmed/33378334 http://dx.doi.org/10.1371/journal.pone.0229051 Text en © 2020 Thomas, Hughes http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Thomas, Merrilee Hughes, Thomas E. Optically activated, customizable, excitable cells |
title | Optically activated, customizable, excitable cells |
title_full | Optically activated, customizable, excitable cells |
title_fullStr | Optically activated, customizable, excitable cells |
title_full_unstemmed | Optically activated, customizable, excitable cells |
title_short | Optically activated, customizable, excitable cells |
title_sort | optically activated, customizable, excitable cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773186/ https://www.ncbi.nlm.nih.gov/pubmed/33378334 http://dx.doi.org/10.1371/journal.pone.0229051 |
work_keys_str_mv | AT thomasmerrilee opticallyactivatedcustomizableexcitablecells AT hughesthomase opticallyactivatedcustomizableexcitablecells |