Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state

Author:

Taylor Keenan C12,Kang Po Wei3ORCID,Hou Panpan3ORCID,Yang Nien-Du3ORCID,Kuenze Georg24,Smith Jarrod A12,Shi Jingyi3,Huang Hui12,White Kelli McFarland3,Peng Dungeng125,George Alfred L6,Meiler Jens247,McFeeters Robert L8,Cui Jianmin3ORCID,Sanders Charles R129ORCID

Affiliation:

1. Department of Biochemistry, Vanderbilt University, Nashville, United States

2. Center for Structural Biology, Vanderbilt University, Nashville, United States

3. Department of Biomedical Engineering, Center for the Investigation of Membrane Excitability Disorders, and Cardiac Bioelectricity, and Arrhythmia Center, Washington University in St. Louis, St. Louis, United States

4. Departments of Chemistry and Pharmacology, Vanderbilt University, Nashville, United States

5. Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, United States

6. Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, United States

7. Department of Bioinformatics, Vanderbilt University Medical Center, Nashville, United States

8. Department of Chemistry, University of Alabama in Huntsville, Huntsville, United States

9. Department of Medicine, Vanderbilt University Medical Center, Nashville, United States

Abstract

Voltage-gated ion channels feature voltage sensor domains (VSDs) that exist in three distinct conformations during activation: resting, intermediate, and activated. Experimental determination of the structure of a potassium channel VSD in the intermediate state has previously proven elusive. Here, we report and validate the experimental three-dimensional structure of the human KCNQ1 voltage-gated potassium channel VSD in the intermediate state. We also used mutagenesis and electrophysiology in Xenopus laevisoocytes to functionally map the determinants of S4 helix motion during voltage-dependent transition from the intermediate to the activated state. Finally, the physiological relevance of the intermediate state KCNQ1 conductance is demonstrated using voltage-clamp fluorometry. This work illuminates the structure of the VSD intermediate state and demonstrates that intermediate state conductivity contributes to the unusual versatility of KCNQ1, which can function either as the slow delayed rectifier current (IKs) of the cardiac action potential or as a constitutively active epithelial leak current.

Funder

National Institutes of Health

American Heart Association

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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