Individual Ion Binding Sites in the K+ Channel Play Distinct Roles in C-type Inactivation and in Recovery from Inactivation

Kimberly Matulef, Alvin W. Annen, Jay C. Nix, Francis Valiyaveetil

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

The selectivity filter of K+ channels contains four ion binding sites (S1-S4) and serves dual functions of discriminating K+ from Na+ and acting as a gate during C-type inactivation. C-type inactivation is modulated by ion binding to the selectivity filter sites, but the underlying mechanism is not known. Here we evaluate how the ion binding sites in the selectivity filter of the KcsA channel participate in C-type inactivation and in recovery from inactivation. We use unnatural amide-to-ester substitutions in the protein backbone to manipulate the S1-S3 sites and a side-chain substitution to perturb the S4 site. We develop an improved semisynthetic approach for generating these amide-to-ester substitutions in the selectivity filter. Our combined electrophysiological and X-ray crystallographic analysis of the selectivity filter mutants show that the ion binding sites play specific roles during inactivation and provide insights into the structural changes at the selectivity filter during C-type inactivation. C-type inactivation in K+ channels results from a conformational change at the ion binding sites. Matulef et al. combine unnatural amide-to-ester substitutions of the protein backbone with structural and functional studies to reveal the specific roles of the individual ion binding sites during inactivation and recovery.

Original languageEnglish (US)
JournalStructure
DOIs
StateAccepted/In press - Dec 29 2015

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Binding Sites
Ions
Amides
Esters
Proteins
X-Rays

ASJC Scopus subject areas

  • Molecular Biology
  • Structural Biology

Cite this

Individual Ion Binding Sites in the K+ Channel Play Distinct Roles in C-type Inactivation and in Recovery from Inactivation. / Matulef, Kimberly; Annen, Alvin W.; Nix, Jay C.; Valiyaveetil, Francis.

In: Structure, 29.12.2015.

Research output: Contribution to journalArticle

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