Cargando…

A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling

BACKGROUND: Animal opsins are light-sensitive G-protein-coupled receptors (GPCRs) that enable optogenetic control over the major heterotrimeric G-protein signaling pathways in animal cells. As such, opsins have potential applications in both biomedical research and therapy. Selecting the opsin with...

Descripción completa

Detalles Bibliográficos
Autores principales: Ballister, Edward R., Rodgers, Jessica, Martial, Franck, Lucas, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771134/
https://www.ncbi.nlm.nih.gov/pubmed/29338718
http://dx.doi.org/10.1186/s12915-017-0475-2
_version_ 1783293207331733504
author Ballister, Edward R.
Rodgers, Jessica
Martial, Franck
Lucas, Robert J.
author_facet Ballister, Edward R.
Rodgers, Jessica
Martial, Franck
Lucas, Robert J.
author_sort Ballister, Edward R.
collection PubMed
description BACKGROUND: Animal opsins are light-sensitive G-protein-coupled receptors (GPCRs) that enable optogenetic control over the major heterotrimeric G-protein signaling pathways in animal cells. As such, opsins have potential applications in both biomedical research and therapy. Selecting the opsin with the best balance of activity and selectivity for a given application requires knowing their ability to couple to a full range of relevant Gα subunits. We present the GsX assay, a set of tools based on chimeric Gs subunits that transduce coupling of opsins to diverse G proteins into increases in cAMP levels,  measured with a real-time reporter in living cells. We use this assay to compare coupling to Gi/o/t across a panel of natural and chimeric opsins selected for potential application in gene therapy for retinal degeneration. RESULTS: Of the opsins tested, wild-type human rod opsin had the highest activity for chimeric Gs proxies for Gi and Gt (Gsi and Gst) and was matched in Go proxy (Gso) activity only by a human rod opsin/scallop opsin chimera. Rod opsin drove roughly equivalent responses via Gsi, Gso, and Gst, while cone opsins showed much lower activities with Gso than Gsi or Gst, and a human rod opsin/amphioxus opsin chimera demonstrated higher activity with Gso than with Gsi or Gst. We failed to detect activity for opsin chimeras bearing three intracellular fragments of mGluR6, and observed unexpectedly complex response profiles for scallop and amphioxus opsins thought to be specialized for Go. CONCLUSIONS: These results identify rod opsin as the most potent non-selective Gi/o/t-coupled opsin, long-wave sensitive cone opsin as the best for selectively activating Gi/t over Go, and a rod opsin/amphioxus opsin chimera as the best choice for selectively activating Go over Gi/t. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0475-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5771134
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-57711342018-01-25 A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling Ballister, Edward R. Rodgers, Jessica Martial, Franck Lucas, Robert J. BMC Biol Research Article BACKGROUND: Animal opsins are light-sensitive G-protein-coupled receptors (GPCRs) that enable optogenetic control over the major heterotrimeric G-protein signaling pathways in animal cells. As such, opsins have potential applications in both biomedical research and therapy. Selecting the opsin with the best balance of activity and selectivity for a given application requires knowing their ability to couple to a full range of relevant Gα subunits. We present the GsX assay, a set of tools based on chimeric Gs subunits that transduce coupling of opsins to diverse G proteins into increases in cAMP levels,  measured with a real-time reporter in living cells. We use this assay to compare coupling to Gi/o/t across a panel of natural and chimeric opsins selected for potential application in gene therapy for retinal degeneration. RESULTS: Of the opsins tested, wild-type human rod opsin had the highest activity for chimeric Gs proxies for Gi and Gt (Gsi and Gst) and was matched in Go proxy (Gso) activity only by a human rod opsin/scallop opsin chimera. Rod opsin drove roughly equivalent responses via Gsi, Gso, and Gst, while cone opsins showed much lower activities with Gso than Gsi or Gst, and a human rod opsin/amphioxus opsin chimera demonstrated higher activity with Gso than with Gsi or Gst. We failed to detect activity for opsin chimeras bearing three intracellular fragments of mGluR6, and observed unexpectedly complex response profiles for scallop and amphioxus opsins thought to be specialized for Go. CONCLUSIONS: These results identify rod opsin as the most potent non-selective Gi/o/t-coupled opsin, long-wave sensitive cone opsin as the best for selectively activating Gi/t over Go, and a rod opsin/amphioxus opsin chimera as the best choice for selectively activating Go over Gi/t. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0475-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-16 /pmc/articles/PMC5771134/ /pubmed/29338718 http://dx.doi.org/10.1186/s12915-017-0475-2 Text en © Rodgers et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ballister, Edward R.
Rodgers, Jessica
Martial, Franck
Lucas, Robert J.
A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling
title A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling
title_full A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling
title_fullStr A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling
title_full_unstemmed A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling
title_short A live cell assay of GPCR coupling allows identification of optogenetic tools for controlling Go and Gi signaling
title_sort live cell assay of gpcr coupling allows identification of optogenetic tools for controlling go and gi signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771134/
https://www.ncbi.nlm.nih.gov/pubmed/29338718
http://dx.doi.org/10.1186/s12915-017-0475-2
work_keys_str_mv AT ballisteredwardr alivecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT rodgersjessica alivecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT martialfranck alivecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT lucasrobertj alivecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT ballisteredwardr livecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT rodgersjessica livecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT martialfranck livecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling
AT lucasrobertj livecellassayofgpcrcouplingallowsidentificationofoptogenetictoolsforcontrollinggoandgisignaling