Published November 22, 2017 | Version v1
Journal article Open

The gating cycle of a K+ channel at atomic resolution

  • 1. Texas Tech University Health Sciences Center
  • 2. University of Chicago

Description

C-type inactivation in potassium channels helps fine-tune long-term channel activity through conformational changes at the selectivity filter. Here, through the use of cross-linked constitutively open constructs, we determined the structures of KcsA's mutants that stabilize the selectivity filter in its conductive (E71A, at 2.25 Å) and deep C-type inactivated (Y82A at 2.4 Å) conformations. These structural snapshots represent KcsA's transient open-conductive (O/O) and the stable open deep C-type inactivated states (O/I), respectively. The present structures provide an unprecedented view of the selectivity filter backbone in its collapsed deep C-type inactivated conformation, highlighting the close interactions with structural waters and the local allosteric interactions that couple activation and inactivation gating. Together with the structures associated with the closed-inactivated state (C/I) and in the well-known closed conductive state (C/O), this work recapitulates, at atomic resolution, the key conformational changes of a potassium channel pore domain as it progresses along its gating cycle.

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Additional details

Identifiers

DOI
10.7554/eLife.28032
Other
oai:uchicago.tind.io:9867

Funding

National Institute of General Medical Sciences
U54 GM087519
Welch Foundation
BI-1757
National Institute of General Medical Sciences
1RO1GM097159-01A1

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Biochemistry and Molecular Biology