Faculty, Staff and Student Publications
Language
English
Publication Date
11-24-2025
Journal
Nature Communications
DOI
10.1038/s41467-025-66730-8
PMID
41285859
PMCID
PMC12748987
PubMedCentral® Posted Date
11-24-2025
PubMedCentral® Full Text Version
Post-print
Abstract
Gi/o protein-coupled receptors (GPCRs) inhibit cardiac and neuronal excitability via G protein-activated K+ channels (GIRK), assembled by combinations of GIRK1 - GIRK4 subunits. GIRKs are activated by direct binding of the Gβγ dimer of inhibitory Gi/o proteins. However, key aspects of this textbook signaling pathway remain debated. Recent studies suggested no Gi/o-GIRK pre-coupling and low (>250 µM) Gβγ-GIRK interaction affinity, contradicting earlier sub-µM estimates and implying low signaling efficiency. We show that Gγ prenylation, which mediates Gβγ membrane attachment required for GIRK activation, also contributes to the Gβγ-GIRK interaction, explaining the poor affinity obtained with non-prenylated Gβγ. Using quantitative protein titration and electrophysiology in live Xenopus oocytes, Gβγ affinity for homotetrameric GIRK2 ranges from 4-30 µM. Heterotetrameric GIRK1/2 shows a higher Gβγ apparent affinity due to the Gβγ-docking site (anchor) in GIRK1, which enriches Gβγ at the channel. Biochemical approaches and molecular dynamic simulations reveal that the Gβγ anchor is formed by interacting N-terminal and distal C-terminal domains of the GIRK1 subunits, distinct from the Gβγ-binding “activation” site(s) underlying channel opening. Thus, the affinity of Gβγ-GIRK interaction is within the expected physiological range, while dynamic pre-coupling of Gβγ to GIRK1-containing channels through high-affinity interactions further enhances the GPCR-Gi/o-GIRK signaling efficiency.
Keywords
G Protein-Coupled Inwardly-Rectifying Potassium Channels, Animals, GTP-Binding Protein beta Subunits, GTP-Binding Protein gamma Subunits, Oocytes, Humans, Xenopus laevis, Signal Transduction, Protein Binding, HEK293 Cells, Potassium channels, Ion channel signalling
Published Open-Access
yes
Recommended Citation
Handklo-Jamal, Reem; Raifman, Tal Keren; Shalomov, Boris; et al., "Live-Cell Quantitative Monitoring Reveals Distinct, High-Affinity Gβγ Regulations of GIRK2 and GIRK1/2 Channels" (2025). Faculty, Staff and Student Publications. 5530.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/5530
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