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Ion-dependent structure, dynamics, and allosteric coupling in a non-selective cation channel.
Lewis, Adam; Kurauskas, Vilius; Tonelli, Marco; Henzler-Wildman, Katherine.
Afiliação
  • Lewis A; Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Kurauskas V; Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Tonelli M; National Magnetic Resonance Facility at Madison (NMRFAM), University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Henzler-Wildman K; Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA. henzlerwildm@wisc.edu.
Nat Commun ; 12(1): 6225, 2021 10 28.
Article em En | MEDLINE | ID: mdl-34711838
ABSTRACT
The selectivity filter (SF) determines which ions are efficiently conducted through ion channel pores. NaK is a non-selective cation channel that conducts Na+ and K+ with equal efficiency. Crystal structures of NaK suggested a rigid SF structure, but later solid-state NMR and MD simulations questioned this interpretation. Here, we use solution NMR to characterize how bound Na+ vs. K+ affects NaK SF structure and dynamics. We find that the extracellular end of the SF is flexible on the ps-ns timescale regardless of bound ion. On a slower timescale, we observe a structural change between the Na+ and K+-bound states, accompanied by increased structural heterogeneity in Na+. We also show direct evidence that the SF structure is communicated to the pore via I88 on the M2 helix. These results support a dynamic SF with multiple conformations involved in non-selective conduction. Our data also demonstrate allosteric coupling between the SF and pore-lining helices in a non-selective cation channel that is analogous to the allosteric coupling previously demonstrated for K+-selective channels, supporting the generality of this model.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Proteínas de Bactérias / Canais de Potássio / Canais de Sódio Idioma: En Revista: Nat Commun Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Proteínas de Bactérias / Canais de Potássio / Canais de Sódio Idioma: En Revista: Nat Commun Ano de publicação: 2021 Tipo de documento: Article