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Ca V 1.1 voltage-sensing domain III exclusively controls skeletal muscle excitation-contraction coupling.
- Source :
-
Nature communications [Nat Commun] 2024 Aug 28; Vol. 15 (1), pp. 7440. Date of Electronic Publication: 2024 Aug 28. - Publication Year :
- 2024
-
Abstract
- Skeletal muscle contractions are initiated by action potentials, which are sensed by the voltage-gated calcium channel (Ca <subscript>V</subscript> 1.1) and are conformationally coupled to calcium release from intracellular stores. Notably, Ca <subscript>V</subscript> 1.1 contains four separate voltage-sensing domains (VSDs), which activate channel gating and excitation-contraction (EC-) coupling at different voltages and with distinct kinetics. Here we show that a single VSD of Ca <subscript>V</subscript> 1.1 controls skeletal muscle EC-coupling. Whereas mutations in VSDs I, II and IV affect the current properties but not EC-coupling, only mutations in VSD III alter the voltage-dependence of depolarization-induced calcium release. Molecular dynamics simulations reveal comprehensive, non-canonical state transitions of VSD III in response to membrane depolarization. Identifying the voltage sensor that activates EC-coupling and detecting its unique conformational changes opens the door to unraveling the downstream events linking VSD III motion to the opening of the calcium release channel, and thus resolving the signal transduction mechanism of skeletal muscle EC-coupling.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Action Potentials physiology
HEK293 Cells
Ion Channel Gating
Muscle Contraction physiology
Mutation
Calcium metabolism
Calcium Channels, L-Type metabolism
Calcium Channels, L-Type genetics
Calcium Channels, L-Type chemistry
Excitation Contraction Coupling
Molecular Dynamics Simulation
Muscle, Skeletal metabolism
Protein Domains
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 15
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 39198449
- Full Text :
- https://doi.org/10.1038/s41467-024-51809-5