Structure of the Shaker Kv channel and mechanism of slow C-type inactivation

Author:

Tan Xiao-Feng1ORCID,Bae Chanhyung1,Stix Robyn23ORCID,Fernández-Mariño Ana I.1ORCID,Huffer Kate13ORCID,Chang Tsg-Hui1,Jiang Jiansen4ORCID,Faraldo-Gómez José D.2ORCID,Swartz Kenton J.1ORCID

Affiliation:

1. Molecular Physiology and Biophysics Section, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.

2. Theoretical Molecular Biophysics Laboratory, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

3. Department of Biology, Johns Hopkins University, 3400 N. Charles Street, Baltimore, MD 21218, USA.

4. Laboratory of Membrane Proteins and Structural Biology and Biophysics Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Abstract

Voltage-activated potassium (Kv) channels open upon membrane depolarization and proceed to spontaneously inactivate. Inactivation controls neuronal firing rates and serves as a form of short-term memory and is implicated in various human neurological disorders. Here, we use high-resolution cryo–electron microscopy and computer simulations to determine one of the molecular mechanisms underlying this physiologically crucial process. Structures of the activated Shaker Kv channel and of its W434F mutant in lipid bilayers demonstrate that C-type inactivation entails the dilation of the ion selectivity filter and the repositioning of neighboring residues known to be functionally critical. Microsecond-scale molecular dynamics trajectories confirm that these changes inhibit rapid ion permeation through the channel. This long-sought breakthrough establishes how eukaryotic K + channels self-regulate their functional state through the plasticity of their selectivity filters.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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