The Isolated Thumb Domain of Acid‐Sensing Ion Channels Forms a Minimal Folding Unit Enabling Ligand Binding Studies

B Biswa P. Mishra B Ben Cristofori‐Armstrong (Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia) E Elena Budusan (School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia) M Mimi Golder (Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia) N Neville J. Butcher (School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia) J Junyu Liu (National Engineering Research Center of Lower-Carbon Catalysis Technology, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Dalian Institute of Chemical Physics) T Theo Crawford (Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia) Y Yanni K.‐Y. Chin (Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia) A Anneka Pereira Schmidt (Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia) X Xinying Jia (Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia) T Taylor B. Smallwood (School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia) R Richard J. Clark J Jan P. Wurm (Bruker Biospin Ettlingen Germany) L Lachlan D. Rash (School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia) M Mehdi Mobli

Abstract

ABSTRACT Proton‐gated acid‐sensing ion channels (ASICs) are emerging therapeutic targets for ischemia‐related conditions such as stroke and myocardial infarction. Although structural data exist for ASIC1a, key aspects of ligand recognition and modulation remain unresolved. Using multidimensional solution‐state NMR spectroscopy, we show that the principal ligand‐binding region of ASICs, the thumb domain, forms an independently folded unit that at neutral pH adopts a native‐like conformation resembling the resting state of the channel. By integrating high‐resolution biophysical analyses of ligand binding to the isolated thumb domain with electrophysiological measurements on full‐length ASIC1a, we distinguished molecular interactions that determine binding affinity from those governing functional efficacy. This approach revealed that dynorphin A acts as a competitive antagonist of ASIC1a. Furthermore, NMR‐based p K a determination of individual acidic residues demonstrated generally elevated values across the isolated thumb domain, supporting the presence of an extended acid‐sensing network rather than a single dominant pH sensor. These findings establish the isolated thumb domain as a powerful model for dissecting ASIC ligand interactions and pH sensitivity in solution, providing mechanistic insights and enabling structure‐based drug discovery of therapeutic modulators for ASICs and related ion channels.

Article Details

Volume / Issue Vol. 65, Issue 19
Published May 04, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (15)

B

Biswa P. Mishra

B

Ben Cristofori‐Armstrong

Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia

E

Elena Budusan

School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia

M

Mimi Golder

Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia

N

Neville J. Butcher

School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia

J

Junyu Liu

National Engineering Research Center of Lower-Carbon Catalysis Technology, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Dalian Institute of Chemical Physics

T

Theo Crawford

Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia

Y

Yanni K.‐Y. Chin

Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia

A

Anneka Pereira Schmidt

Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia

X

Xinying Jia

Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Queensland Australia

T

Taylor B. Smallwood

School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia

R

Richard J. Clark

J

Jan P. Wurm

Bruker Biospin Ettlingen Germany

L

Lachlan D. Rash

School of Biomedical Sciences The University of Queensland St Lucia Queensland Australia

M

Mehdi Mobli