Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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
_version_ 1783598238112153600
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
work_keys_str_mv AT shaayamark lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT fauserjordan lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT zhurikhinaanastasia lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT conagepoughjasone lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT huyotvincent lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT brennanmartin lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT flowercameront lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT matschejacob lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT khanshahzeb lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT natarajanviswanathan lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT rehmanjalees lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT kotapradeep lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT whiteforestm lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT tsygankovdenis lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity
AT karginovandreiv lightregulatedallostericswitchenablestemporalandsubcellularcontrolofenzymeactivity