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Voltage-dependent G-protein regulation of CaV2.2 (N-type) channels
Linköping University, Department of Biomedical and Clinical Sciences, The Division of Cell and Neurobiology. Linköping University, Faculty of Medicine and Health Sciences. (Pantazis)ORCID iD: 0000-0002-0891-7732
Linköping University, Department of Biomedical and Clinical Sciences, The Division of Cell and Neurobiology. Linköping University, Faculty of Medicine and Health Sciences. (Pantazis)ORCID iD: 0000-0002-6315-8732
Linköping University, Department of Biomedical and Clinical Sciences, The Division of Cell and Neurobiology. Linköping University, Faculty of Medicine and Health Sciences. (Pantazis)ORCID iD: 0000-0001-8049-3869
Department of Anesthesiology and Perioperative Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.. (Olcese)ORCID iD: 0000-0003-4621-3784
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2024 (English)In: Science Advances, E-ISSN 2375-2548, Vol. 10, no 37, article id eadp6665Article in journal (Refereed) Published
Abstract [en]

How G proteins inhibit N-type, voltage-gated, calcium-selective channels (CaV2.2) during presynaptic inhibition is a decades-old question. G proteins Gβγ bind to intracellular CaV2.2 regions, but the inhibition is voltage dependent. Using the hybrid electrophysiological and optical approach voltage-clamp fluorometry, we show that Gβγ acts by selectively inhibiting a subset of the four different CaV2.2 voltage-sensor domains (VSDs I to IV). During regular “willing” gating, VSD-I and -IV activations resemble pore opening, VSD III activation is hyperpolarized, and VSD II appears unresponsive to depolarization. In the presence of Gβγ, CaV2.2 gating is “reluctant”: pore opening and VSD I activation are strongly and proportionally inhibited, VSD IV is modestly inhibited, while VSD III is not. We propose that Gβγ inhibition of VSDs I and IV underlies reluctant CaV2.2 gating and subsequent presynaptic inhibition.

Place, publisher, year, edition, pages
AMER ASSOC ADVANCEMENT SCIENCE , 2024. Vol. 10, no 37, article id eadp6665
National Category
Neurosciences Physiology and Anatomy Biochemistry Molecular Biology Biophysics Structural Biology
Identifiers
URN: urn:nbn:se:liu:diva-207602DOI: 10.1126/sciadv.adp6665ISI: 001310268400005PubMedID: 39259796OAI: oai:DiVA.org:liu-207602DiVA, id: diva2:1897496
Funder
Swedish Research Council, 2019-00988Swedish Research Council, 2022-00574The Swedish Brain Foundation, FO2022-0003The Swedish Brain Foundation, FO2023-0025Knut and Alice Wallenberg FoundationNIH (National Institutes of Health), R35GM131896
Note

Funding Agencies|Lions Forskningsfond Ph.D. program; NIH/NIGMS [R35GM131896]; Linkoeping University Wallenberg Center for Molecular Medicine/the Knut and Alice Wallenberg Foundation; Hjarnfonden (The Swedish Brain Foundation) [FO2022-0003, FO2023-0025]; Vetenskapsradet (The Swedish Research Council) [2019-00988, 2022-00574]

Available from: 2024-09-13 Created: 2024-09-13 Last updated: 2025-04-19

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Nilsson, MichelleWang, KaiqianMínguez-Viñas, TeresaBerglund, StinaPantazis, Antonios

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