Structural insights in the permeation mechanism of an activated GIRK2 channel

G protein-gated inwardly rectifying potassium (GIRK) channels play a significant role in physiopathology by the regulation of cell excitability. This regulation depends on the K+ ion conduction induced by structural constrictions: the selectivity filters (SFs), helix bundle crossings (HBCs), and G-l...

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Veröffentlicht in:Biochimica et biophysica acta. Biomembranes 2024-01, Vol.1866 (1), p.184231-184231, Article 184231
Hauptverfasser: Li, Dailin, Shi, Dingyuan, Wang, Lei
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Shi, Dingyuan
Wang, Lei
description G protein-gated inwardly rectifying potassium (GIRK) channels play a significant role in physiopathology by the regulation of cell excitability. This regulation depends on the K+ ion conduction induced by structural constrictions: the selectivity filters (SFs), helix bundle crossings (HBCs), and G-loop gates. To explore why no permeation occurred when the constrictions were kept in the open state, a 4-K+-related occupancy mechanism was proposed. Unfortunately, this hypothesis was neither assessed, nor was the energetic characteristics presented. To identify the permeation mechanism on an atomic level, all-atom molecular dynamic (MD) simulations and a coupled quantum mechanics and molecular mechanics (QM/MM) method were used for the GIRK2 mutant R201A. It was found that the R201A had a moderate conductive capability in the presence of PIP2. Furthermore, the 4-K+ group of ions was found to dominate the conduction through the activated HBC gate. This shielding-like mechanism was assessed by the potential energy barrier along the conduction pathway. Mutation studies did further support the assumption that E152 was responsible for the mechanism. Moreover, E152 was most probably facilitating the inflow of ions from the SF to the cavity. On the contrary, N184 had no remarkable effect on this mechanism, except for the conduction efficiency. These findings highlighted the necessity of a multi-ion distribution for the conduction to take place, and indicated that the K+ migration was not only determined by the channel conductive state in the GIRK channel. The here presented multi-ion permeation mechanism may help to provide an effective way to regulate the channelopathies. [Display omitted] •4-K+ group of ions dominates K+ conduction through an activated HBC gate.•4-K+ pattern functions with a shielding-like mechanism.•E152 is responsible for the mechanism and probably facilitating inflow of K+ ions.•Necessity of a multi-ion distribution for K+ conduction is highlighted.
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Mutation studies did further support the assumption that E152 was responsible for the mechanism. Moreover, E152 was most probably facilitating the inflow of ions from the SF to the cavity. On the contrary, N184 had no remarkable effect on this mechanism, except for the conduction efficiency. These findings highlighted the necessity of a multi-ion distribution for the conduction to take place, and indicated that the K+ migration was not only determined by the channel conductive state in the GIRK channel. The here presented multi-ion permeation mechanism may help to provide an effective way to regulate the channelopathies. [Display omitted] •4-K+ group of ions dominates K+ conduction through an activated HBC gate.•4-K+ pattern functions with a shielding-like mechanism.•E152 is responsible for the mechanism and probably facilitating inflow of K+ ions.•Necessity of a multi-ion distribution for K+ conduction is highlighted.</description><identifier>ISSN: 0005-2736</identifier><identifier>EISSN: 1879-2642</identifier><identifier>DOI: 10.1016/j.bbamem.2023.184231</identifier><identifier>PMID: 37739205</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>G Protein-Coupled Inwardly-Rectifying Potassium Channels - chemistry ; G Protein-Coupled Inwardly-Rectifying Potassium Channels - metabolism ; GIRK ; GTP-Binding Proteins - metabolism ; Ions - metabolism ; Molecular Dynamics Simulation ; Mutation ; Permeation mechanism ; QM/MM</subject><ispartof>Biochimica et biophysica acta. 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Biomembranes</title><addtitle>Biochim Biophys Acta Biomembr</addtitle><description>G protein-gated inwardly rectifying potassium (GIRK) channels play a significant role in physiopathology by the regulation of cell excitability. This regulation depends on the K+ ion conduction induced by structural constrictions: the selectivity filters (SFs), helix bundle crossings (HBCs), and G-loop gates. To explore why no permeation occurred when the constrictions were kept in the open state, a 4-K+-related occupancy mechanism was proposed. Unfortunately, this hypothesis was neither assessed, nor was the energetic characteristics presented. To identify the permeation mechanism on an atomic level, all-atom molecular dynamic (MD) simulations and a coupled quantum mechanics and molecular mechanics (QM/MM) method were used for the GIRK2 mutant R201A. It was found that the R201A had a moderate conductive capability in the presence of PIP2. Furthermore, the 4-K+ group of ions was found to dominate the conduction through the activated HBC gate. This shielding-like mechanism was assessed by the potential energy barrier along the conduction pathway. Mutation studies did further support the assumption that E152 was responsible for the mechanism. Moreover, E152 was most probably facilitating the inflow of ions from the SF to the cavity. On the contrary, N184 had no remarkable effect on this mechanism, except for the conduction efficiency. These findings highlighted the necessity of a multi-ion distribution for the conduction to take place, and indicated that the K+ migration was not only determined by the channel conductive state in the GIRK channel. The here presented multi-ion permeation mechanism may help to provide an effective way to regulate the channelopathies. 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Mutation studies did further support the assumption that E152 was responsible for the mechanism. Moreover, E152 was most probably facilitating the inflow of ions from the SF to the cavity. On the contrary, N184 had no remarkable effect on this mechanism, except for the conduction efficiency. These findings highlighted the necessity of a multi-ion distribution for the conduction to take place, and indicated that the K+ migration was not only determined by the channel conductive state in the GIRK channel. The here presented multi-ion permeation mechanism may help to provide an effective way to regulate the channelopathies. [Display omitted] •4-K+ group of ions dominates K+ conduction through an activated HBC gate.•4-K+ pattern functions with a shielding-like mechanism.•E152 is responsible for the mechanism and probably facilitating inflow of K+ ions.•Necessity of a multi-ion distribution for K+ conduction is highlighted.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>37739205</pmid><doi>10.1016/j.bbamem.2023.184231</doi><tpages>1</tpages></addata></record>
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subjects G Protein-Coupled Inwardly-Rectifying Potassium Channels - chemistry
G Protein-Coupled Inwardly-Rectifying Potassium Channels - metabolism
GIRK
GTP-Binding Proteins - metabolism
Ions - metabolism
Molecular Dynamics Simulation
Mutation
Permeation mechanism
QM/MM
title Structural insights in the permeation mechanism of an activated GIRK2 channel
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