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Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity
Engineered allosteric regulation of protein activity provides significant advantages for the development of robust and broadly applicable tools. However, the application of allosteric switches in optogenetics has been scarce and suffers from critical limitations. Here, we report an optogenetic appro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577742/ https://www.ncbi.nlm.nih.gov/pubmed/32965214 http://dx.doi.org/10.7554/eLife.60647 |
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author | Shaaya, Mark Fauser, Jordan Zhurikhina, Anastasia Conage-Pough, Jason E Huyot, Vincent Brennan, Martin Flower, Cameron T Matsche, Jacob Khan, Shahzeb Natarajan, Viswanathan Rehman, Jalees Kota, Pradeep White, Forest M Tsygankov, Denis Karginov, Andrei V |
author_facet | Shaaya, Mark Fauser, Jordan Zhurikhina, Anastasia Conage-Pough, Jason E Huyot, Vincent Brennan, Martin Flower, Cameron T Matsche, Jacob Khan, Shahzeb Natarajan, Viswanathan Rehman, Jalees Kota, Pradeep White, Forest M Tsygankov, Denis Karginov, Andrei V |
author_sort | Shaaya, Mark |
collection | PubMed |
description | Engineered allosteric regulation of protein activity provides significant advantages for the development of robust and broadly applicable tools. However, the application of allosteric switches in optogenetics has been scarce and suffers from critical limitations. Here, we report an optogenetic approach that utilizes an engineered Light-Regulated (LightR) allosteric switch module to achieve tight spatiotemporal control of enzymatic activity. Using the tyrosine kinase Src as a model, we demonstrate efficient regulation of the kinase and identify temporally distinct signaling responses ranging from seconds to minutes. LightR-Src off-kinetics can be tuned by modulating the LightR photoconversion cycle. A fast cycling variant enables the stimulation of transient pulses and local regulation of activity in a selected region of a cell. The design of the LightR module ensures broad applicability of the tool, as we demonstrate by achieving light-mediated regulation of Abl and bRaf kinases as well as Cre recombinase. |
format | Online Article Text |
id | pubmed-7577742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75777422020-10-23 Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity Shaaya, Mark Fauser, Jordan Zhurikhina, Anastasia Conage-Pough, Jason E Huyot, Vincent Brennan, Martin Flower, Cameron T Matsche, Jacob Khan, Shahzeb Natarajan, Viswanathan Rehman, Jalees Kota, Pradeep White, Forest M Tsygankov, Denis Karginov, Andrei V eLife Biochemistry and Chemical Biology Engineered allosteric regulation of protein activity provides significant advantages for the development of robust and broadly applicable tools. However, the application of allosteric switches in optogenetics has been scarce and suffers from critical limitations. Here, we report an optogenetic approach that utilizes an engineered Light-Regulated (LightR) allosteric switch module to achieve tight spatiotemporal control of enzymatic activity. Using the tyrosine kinase Src as a model, we demonstrate efficient regulation of the kinase and identify temporally distinct signaling responses ranging from seconds to minutes. LightR-Src off-kinetics can be tuned by modulating the LightR photoconversion cycle. A fast cycling variant enables the stimulation of transient pulses and local regulation of activity in a selected region of a cell. The design of the LightR module ensures broad applicability of the tool, as we demonstrate by achieving light-mediated regulation of Abl and bRaf kinases as well as Cre recombinase. eLife Sciences Publications, Ltd 2020-09-23 /pmc/articles/PMC7577742/ /pubmed/32965214 http://dx.doi.org/10.7554/eLife.60647 Text en © 2020, Shaaya et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Shaaya, Mark Fauser, Jordan Zhurikhina, Anastasia Conage-Pough, Jason E Huyot, Vincent Brennan, Martin Flower, Cameron T Matsche, Jacob Khan, Shahzeb Natarajan, Viswanathan Rehman, Jalees Kota, Pradeep White, Forest M Tsygankov, Denis Karginov, Andrei V Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
title | Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
title_full | Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
title_fullStr | Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
title_full_unstemmed | Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
title_short | Light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
title_sort | light-regulated allosteric switch enables temporal and subcellular control of enzyme activity |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577742/ https://www.ncbi.nlm.nih.gov/pubmed/32965214 http://dx.doi.org/10.7554/eLife.60647 |
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