Atomistic Mechanism of Calcium-Mediated Inward Rectification of the MthK Potassium Channel by Solid-State NMR and MD Simulations

Inward rectification is a fundamental but poorly understood phenomenon in potassium channel physiology. Despite its physiological importance, the exact mechanism has remained elusive. In this work, we uncover a previously unrecognized calcium-mediated gating mechanism in the MthK potassium channel that sheds new light on this essential process. By combining state-of-the-art proton-detected solid-state NMR spectroscopy with atomistic molecular dynamics simulations, we reveal that divalent calcium ions bind below the selectivity filter, physically obstructing the outward flow of potassium ions whereas inward flow is still possible─analogous to a molecular ball check valve. Second, the binding of Ca<sup>2+</sup> to this site leads to stabilization of the selectivity filter and allows us to directly observe ion-ion interactions in the filter. These results offer direct experimental support for the long-debated "direct knock-on" mechanism, in which potassium ions move through the filter, without water cotransport.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-01
DOI
https://doi.org/10.1021/jacs.5c16155
Citations
1
Primary Topic
Ion channel regulation and function
Type
article
Field-Weighted Citation Impact
0.81
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article

Atomistic Mechanism of Calcium-Mediated Inward Rectification of the MthK Potassium Channel by Solid-State NMR and MD Simulations

Carl Öster, Chaowei Shi, Wojciech Kopeć, Ronald de Vries et al.
1 citations
Journal of the American Chemical Society
Ion channel regulation and function
0.81
article

Atomistic Mechanism of Calcium-Mediated Inward Rectification of the MthK Potassium Channel by Solid-State NMR and MD Simulations

Carl Öster, Chaowei Shi, Wojciech Kopeć, Ronald de Vries, Bert L. de Groot, Adam Lange, Sascha Lange, Juan Li, Denis Qoraj
article en
1 citations

Abstract

Inward rectification is a fundamental but poorly understood phenomenon in potassium channel physiology. Despite its physiological importance, the exact mechanism has remained elusive. In this work, we uncover a previously unrecognized calcium-mediated gating mechanism in the MthK potassium channel that sheds new light on this essential process. By combining state-of-the-art proton-detected solid-state NMR spectroscopy with atomistic molecular dynamics simulations, we reveal that divalent calcium ions bind below the selectivity filter, physically obstructing the outward flow of potassium ions whereas inward flow is still possible─analogous to a molecular ball check valve. Second, the binding of Ca<sup>2+</sup> to this site leads to stabilization of the selectivity filter and allows us to directly observe ion-ion interactions in the filter. These results offer direct experimental support for the long-debated "direct knock-on" mechanism, in which potassium ions move through the filter, without water cotransport.

Journal of the American Chemical SocietyVol. 147(49)
University of Science and Technology of China (CN), Queen Mary University of London (GB), Humboldt-Universität zu Berlin (DE), Max Planck Institute for Dynamics and Self-Organization (DE), Leibniz-Forschungsinstitut für Molekulare Pharmakologie (DE), Hefei National Center for Physical Sciences at Nanoscale (CN), Max Planck Institute for Multidisciplinary Sciences (DE), Life University (US)
Openalex Percentile: Top 21%
Ion channel regulation and function
0.81
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