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CaMello-XR enables visualization and optogenetic control of Gq/11 signals and receptor trafficking in GPCR-specific domains.


ABSTRACT: The signal specificity of G protein-coupled receptors (GPCRs) including serotonin receptors (5-HT-R) depends on the trafficking and localization of the GPCR within its subcellular signaling domain. Visualizing traffic-dependent GPCR signals in neurons is difficult, but important to understand the contribution of GPCRs to synaptic plasticity. We engineered CaMello (Ca2+-melanopsin-local-sensor) and CaMello-5HT2A for visualization of traffic-dependent Ca2+ signals in 5-HT2A-R domains. These constructs consist of the light-activated Gq/11 coupled melanopsin, mCherry and GCaMP6m for visualization of Ca2+ signals and receptor trafficking, and the 5-HT2A C-terminus for targeting into 5-HT2A-R domains. We show that the specific localization of the GPCR to its receptor domain drastically alters the dynamics and localization of the intracellular Ca2+ signals in different neuronal populations in vitro and in vivo. The CaMello method may be extended to every GPCR coupling to the Gq/11 pathway to help unravel new receptor-specific functions in respect to synaptic plasticity and GPCR localization.

SUBMITTER: Eickelbeck D 

PROVIDER: S-EPMC6376006 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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CaMello-XR enables visualization and optogenetic control of G<sub>q/11</sub> signals and receptor trafficking in GPCR-specific domains.

Eickelbeck Dennis D   Karapinar Raziye R   Jack Alexander A   Suess Sandra T ST   Barzan Ruxandra R   Azimi Zohre Z   Surdin Tatjana T   Grömmke Michelle M   Mark Melanie D MD   Gerwert Klaus K   Jancke Dirk D   Wahle Petra P   Spoida Katharina K   Herlitze Stefan S  

Communications biology 20190214


The signal specificity of G protein-coupled receptors (GPCRs) including serotonin receptors (5-HT-R) depends on the trafficking and localization of the GPCR within its subcellular signaling domain. Visualizing traffic-dependent GPCR signals in neurons is difficult, but important to understand the contribution of GPCRs to synaptic plasticity. We engineered CaMello (Ca<sup>2+</sup>-melanopsin-local-sensor) and CaMello-5HT<sub>2A</sub> for visualization of traffic-dependent Ca<sup>2+</sup> signals  ...[more]

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