Related ArticlesConformational equilibrium shift underlies altered K+ channel gating as revealed by NMR.
Nat Commun. 2020 10 14;11(1):5168
Authors: Iwahashi Y, Toyama Y, Imai S, Itoh H, Osawa M, Inoue M, Shimada I
Abstract
The potassium ion (K+) channel plays a fundamental role in controlling K+ permeation across the cell membrane and regulating cellular excitabilities. Mutations in the transmembrane pore reportedly affect the gating transitions of K+ channels, and are associated with the onset of neural disorders. However, due to the lack of structural and dynamic insights into the functions of K+ channels, the structural mechanism by which these mutations cause K+ channel dysfunctions remains elusive. Here, we used nuclear magnetic resonance spectroscopy to investigate the structural mechanism underlying the decreased K+-permeation caused by disease-related mutations, using the prokaryotic K+ channel KcsA. We demonstrated that the conformational equilibrium in the transmembrane region is shifted toward the non-conductive state with the closed intracellular K+-gate in the disease-related mutant. We also demonstrated that this equilibrium shift is attributable to the additional steric contacts in the open-conductive structure, which are evoked by the increased side-chain bulkiness of the residues lining the transmembrane helix. Our results suggest that the alteration in the conformational equilibrium of the intracellular K+-gate is one of the fundamental mechanisms underlying the dysfunctions of K+ channels caused by disease-related mutations.
[ASAP] Gating Mechanism of Aquaporin Z in Synthetic Bilayers and Native Membranes Revealed by Solid-State NMR Spectroscopy
Gating Mechanism of Aquaporin Z in Synthetic Bilayers and Native Membranes Revealed by Solid-State NMR Spectroscopy
Yongxiang Zhao, Huayong Xie, Lili Wang, Yang Shen, Wei Chen, Benteng Song, Zhengfeng Zhang, Anmin Zheng, Qingsong Lin, Riqiang Fu, Jufang Wang, Jun Yang
https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.8b03446/20180611/images/medium/ja-2018-03446h_0009.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.8b03446
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA...
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[NMR paper] Gating Mechanism of Aquaporin Z in Synthetic Bilayers and Native Membranes Revealed by Solid-state NMR Spectroscopy.
Gating Mechanism of Aquaporin Z in Synthetic Bilayers and Native Membranes Revealed by Solid-state NMR Spectroscopy.
Related Articles Gating Mechanism of Aquaporin Z in Synthetic Bilayers and Native Membranes Revealed by Solid-state NMR Spectroscopy.
J Am Chem Soc. 2018 May 25;:
Authors: Zhao Y, Xie H, Wang L, Shen Y, Chen W, Song B, Zhang Z, Zheng A, Lin Q, Fu R, Wang J, Yang J
Abstract
Aquaporin Z (AqpZ) is an integral membrane protein that facilitates transport of water across E. coli cells with a high rate. Previously, R189,...
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05-29-2018 06:45 PM
[NMR paper] Interplay Between Membrane Curvature and Protein Conformational Equilibrium Investigated by Solid-State NMR.
Interplay Between Membrane Curvature and Protein Conformational Equilibrium Investigated by Solid-State NMR.
Interplay Between Membrane Curvature and Protein Conformational Equilibrium Investigated by Solid-State NMR.
J Struct Biol. 2018 Feb 28;:
Authors: Liao SY, Lee M, Hong M
Abstract
Many membrane proteins sense and induce membrane curvature for function, but structural information about how proteins modulate their structures to cause membrane curvature is sparse. We review our recent solid-state NMR studies of two virus...
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Interplay Between Membrane Curvature and Protein Conformational Equilibrium Investigated by Solid-State NMR
Interplay Between Membrane Curvature and Protein Conformational Equilibrium Investigated by Solid-State NMR
Publication date: Available online 1 March 2018
Source:Journal of Structural Biology</br>
Author(s): Shu Y. Liao, Myungwoon Lee, Mei Hong</br>
Many membrane proteins sense and induce membrane curvature for function, but structural information about how proteins modulate their structures to cause membrane curvature is sparse. We review our recent solid-state NMR studies of two virus membrane proteins whose conformational equilibrium is tightly coupled to...
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03-01-2018 09:20 PM
[NMR paper] Characterization of conformational dynamics of bistable RNA by equilibrium and non-equilibrium NMR.
Characterization of conformational dynamics of bistable RNA by equilibrium and non-equilibrium NMR.
Characterization of conformational dynamics of bistable RNA by equilibrium and non-equilibrium NMR.
Curr Protoc Nucleic Acid Chem. 2014;55:11.13.1-11.13.16
Authors: Fürtig B, Reining A, Sochor F, Oberhauser EM, Heckel A, Schwalbe H
Abstract
Unlike proteins, a given RNA sequence can adopt more than a single conformation. The two (or more) conformations are long-lived and have similar stabilities, but interconvert only slowly. Such...
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01-30-2015 12:15 PM
[NMR paper] pH-Dependent Conformation, Dynamics, and Aromatic Interaction of*the*Gating Tryptophan Residue of the Influenza M2 Proton Channel from*Solid-State NMR.
pH-Dependent Conformation, Dynamics, and Aromatic Interaction of*the*Gating Tryptophan Residue of the Influenza M2 Proton Channel from*Solid-State NMR.
Related Articles pH-Dependent Conformation, Dynamics, and Aromatic Interaction of*the*Gating Tryptophan Residue of the Influenza M2 Proton Channel from*Solid-State NMR.
Biophys J. 2013 Apr 16;104(8):1698-708
Authors: Williams JK, Zhang Y, Schmidt-Rohr K, Hong M
Abstract
The M2 protein of the influenza virus conducts protons into the virion under external acidic pH. The proton selectivity of...
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04-23-2013 08:37 PM
[NMR paper] Determination of conformational equilibrium of peptides in solution by NMR spectrosco
Determination of conformational equilibrium of peptides in solution by NMR spectroscopy and theoretical conformational analysis: application to the calibration of mean-field solvation models.
Related Articles Determination of conformational equilibrium of peptides in solution by NMR spectroscopy and theoretical conformational analysis: application to the calibration of mean-field solvation models.
Biopolymers. 2001;60(2):79-95
Authors: Groth M, Malicka J, Rodziewicz- Motowid?o S, Czaplewski C, Klaudel L, Wiczk W, Liwo A
Peptides occur in...
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[NMR paper] A conformational equilibrium in a protein fragment caused by two consecutive capping
A conformational equilibrium in a protein fragment caused by two consecutive capping boxes: 1H-, 13C-NMR, and mutational analysis.
Related Articles A conformational equilibrium in a protein fragment caused by two consecutive capping boxes: 1H-, 13C-NMR, and mutational analysis.
Protein Sci. 1998 Jul;7(7):1506-15
Authors: Guerois R, Cordier-Ochsenbein F, Baleux F, Huynh-Dinh T, Neumann JM, Sanson A
The conformational properties of an 18 residues peptide spanning the entire sequence, L1KTPA5QFDAD10ELRAA15MKG, of the first helix (A-helix) of...