Instantaneous ion configurations in the K + ion channel selectivity filter revealed by 2D IR spectroscopy

Author:

Kratochvil Huong T.1,Carr Joshua K.1,Matulef Kimberly2,Annen Alvin W.2,Li Hui3,Maj Michał1,Ostmeyer Jared3,Serrano Arnaldo L.1,Raghuraman H.3,Moran Sean D.1,Skinner J. L.1,Perozo Eduardo3,Roux Benoît3,Valiyaveetil Francis I.2,Zanni Martin T.1

Affiliation:

1. Department of Chemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.

2. Program in Chemical Biology, Department of Physiology and Pharmacology, Oregon Health and Science University, Portland, OR 97239, USA.

3. Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA.

Abstract

Potassium channels are responsible for the selective permeation of K + ions across cell membranes. K + ions permeate in single file through the selectivity filter, a narrow pore lined by backbone carbonyls that compose four K + binding sites. Here, we report on the two-dimensional infrared (2D IR) spectra of a semisynthetic KcsA channel with site-specific heavy ( 13 C 18 O) isotope labels in the selectivity filter. The ultrafast time resolution of 2D IR spectroscopy provides an instantaneous snapshot of the multi-ion configurations and structural distributions that occur spontaneously in the filter. Two elongated features are resolved, revealing the statistical weighting of two structural conformations. The spectra are reproduced by molecular dynamics simulations of structures with water separating two K + ions in the binding sites, ruling out configurations with ions occupying adjacent sites.

Funder

U.S. National Institutes of Health

University of Wisconsin Foundation

NIH

Membrane Protein Structural Dynamics Consortium

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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