Unanticipated parallels in architecture and mechanism between ATP-gated P2X receptors and acid sensing ion channels

Isabelle Baconguis, Motoyuki Hattori, Eric Gouaux

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

ATP-gated P2X receptors and acid-sensing ion channels are cation-selective, trimeric ligand-gated ion channels unrelated in amino acid sequence. Nevertheless, initial crystal structures of the P2X4 receptor and acid-sensing ion channel 1a in resting/closed and in non conductive/desensitized conformations, respectively, revealed common elements of architecture. Recent structures of both channels have revealed the ion channels in open conformations. Here we focus on common elements of architecture, conformational change and ion permeation, emphasizing general principles of structure and mechanism in P2X receptors and in acid-sensing ion channels and showing how these two sequence-disparate families of ligand-gated ion channel harbor unexpected similarities when viewed through a structural lens.

Original languageEnglish (US)
Pages (from-to)277-284
Number of pages8
JournalCurrent Opinion in Structural Biology
Volume23
Issue number2
DOIs
StatePublished - Apr 2013

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Acid Sensing Ion Channels
Ligand-Gated Ion Channels
Adenosine Triphosphate
Purinergic P2X4 Receptors
Ion Channels
Lenses
Cations
Amino Acid Sequence
Ions

ASJC Scopus subject areas

  • Molecular Biology
  • Structural Biology

Cite this

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