» Articles » PMID: 27796578

Upward Movement of IS4 and IIIS4 is a Rate-limiting Stage in Ca1.2 Activation

Overview
Journal Pflugers Arch
Specialty Physiology
Date 2016 Nov 1
PMID 27796578
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

In order to specify the role of individual S4 segments in Ca1.2 gating, charged residues of segments IS4-IVS4 were replaced by glutamine and the corresponding effects on activation/deactivation of calcium channel currents were analysed. Almost all replacements of charges in IS4 and IIIS4 decreased the slope of the Boltzmann curve of channel activation (activation curve) while charge neutralisations in IIS4 and IVS4 did not significantly affect the slope. S4 mutations caused either left or rightward shifts of the activation curve, and in wild-type channels, these S4 mutations hardly affected current kinetics.In slowly gating pore (S6) mutants (G432W, A780T, G1193T or A1503G), neutralisations in S4 segments significantly accelerated current kinetics. Likewise in wild type, charge replacements in IS4 and IIIS4 of pore mutants reduced the slope of the activation curves while substitutions of charges in IIS4 and IVS4 had less or no impact. We propose a gating model where the structurally different S4 segments leave their resting positions not simultaneously. Upward movement of segments IS4 and (to a lesser extend) IIIS4 appear to be a rate-limiting stage for releasing the pore gates. These segments carry most of the effective charge for channel activation. Our study suggests that S4 segments of Ca1.2 control the closed state in domain specific manner while stabilizing the open state in a non-specific manner.

Citing Articles

Functional Characterization of Four Known Cav2.1 Variants Associated with Neurodevelopmental Disorders.

Folacci M, Estaran S, Menard C, Bertaud A, Rousset M, Roussel J Membranes (Basel). 2023; 13(1).

PMID: 36676903 PMC: 9864995. DOI: 10.3390/membranes13010096.


Role of High Voltage-Gated Ca Channel Subunits in Pancreatic β-Cell Insulin Release. From Structure to Function.

Tuluc P, Theiner T, Jacobo-Piqueras N, Geisler S Cells. 2021; 10(8).

PMID: 34440773 PMC: 8393260. DOI: 10.3390/cells10082004.


Permeabilizing Cell Membranes with Electric Fields.

Aguilar A, Ho M, Chang E, Carlson K, Natarajan A, Marciano T Cancers (Basel). 2021; 13(9).

PMID: 34068775 PMC: 8126200. DOI: 10.3390/cancers13092283.


Ca2.3 channel function and Zn-induced modulation: potential mechanisms and (patho)physiological relevance.

Neumaier F, Schneider T, Albanna W Channels (Austin). 2020; 14(1):362-379.

PMID: 33079629 PMC: 7583514. DOI: 10.1080/19336950.2020.1829842.


Zn2+-induced changes in Cav2.3 channel function: An electrophysiological and modeling study.

Neumaier F, Alpdogan S, Hescheler J, Schneider T J Gen Physiol. 2020; 152(9).

PMID: 32559275 PMC: 7478874. DOI: 10.1085/jgp.202012585.


References
1.
Hamill O, Marty A, Neher E, Sakmann B, Sigworth F . Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981; 391(2):85-100. DOI: 10.1007/BF00656997. View

2.
Wu J, Yan Z, Li Z, Yan C, Lu S, Dong M . Structure of the voltage-gated calcium channel Cav1.1 complex. Science. 2015; 350(6267):aad2395. DOI: 10.1126/science.aad2395. View

3.
Ledwell J, Aldrich R . Mutations in the S4 region isolate the final voltage-dependent cooperative step in potassium channel activation. J Gen Physiol. 1999; 113(3):389-414. PMC: 2222902. DOI: 10.1085/jgp.113.3.389. View

4.
Karmazinova M, Lacinova L . Removal of the outermost arginine in IVS4 segment of the Ca(V)3.1 channel affects amplitude but not voltage dependence of gating current. Gen Physiol Biophys. 2010; 29(4):419-23. DOI: 10.4149/gpb_2010_04_419. View

5.
Payandeh J, Gamal El-Din T, Scheuer T, Zheng N, Catterall W . Crystal structure of a voltage-gated sodium channel in two potentially inactivated states. Nature. 2012; 486(7401):135-9. PMC: 3552482. DOI: 10.1038/nature11077. View