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Determinants of ion selectivity in ASIC1a- and ASIC2a-containing acid-sensing ion channels

journal contribution
posted on 2024-11-02, 11:48 authored by Timothy Lynagh, Emelie Flood, Celine Boiteux, Zeshan Sheikh, Toby AllenToby Allen, Stephan Pless
Trimeric acid-sensing ion channels (ASICs) contribute to neuronal signaling by converting extracellular acidification into excitatory sodium currents. Previous work with homomeric ASIC1a implicates conserved leucine (L7') and consecutive glycine-alanine-serine (GAS belt) residues near the middle, and conserved negatively charged (E18') residues at the bottom of the pore in ion permeation and/or selectivity. However, a conserved mechanism of ion selectivity throughout the ASIC family has not been established. We therefore explored the molecular determinants of ion selectivity in heteromeric ASIC1a/ASIC2a and homomeric ASIC2a channels using site-directed mutagenesis, electrophysiology, and molecular dynamics free energy simulations. Similar to ASIC1a, E18' residues create an energetic preference for sodium ions at the lower end of the pore in ASIC2a-containing channels. However, and in contrast to ASIC1a homomers, ion permeation through ASIC2a-containing channels is not determined by L7' side chains in the upper part of the channel. This may be, in part, due to ASIC2a-specific negatively charged residues (E59 and E62) that lower the energy of ions in the upper pore, thus making the GAS belt more important for selectivity. This is confirmed by experiments showing that the L7'A mutation has no effect in ASIC2a, in contrast to ASIC1a, where it eliminated selectivity. ASIC2a triple mutants eliminating both L7' and upper charges did not lead to large changes in selectivity, suggesting a different role for L7' in ASIC2a compared with ASIC1a channels. In contrast, we observed measurable changes in ion selectivity in ASIC2a-containing channels with GAS belt mutations. Our results suggest that ion conduction and selectivity in the upper part of the ASIC pore may differ between subtypes, whereas the essential role of E18' in ion selectivity is conserved. Furthermore, we demonstrate that heteromeric channels containing mutations in only one of two ASIC subty

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Related Materials

  1. 1.
    DOI - Is published in 10.1085/jgp.201812297
  2. 2.
    ISSN - Is published in 15407748

Journal

The Journal of general physiology

Volume

152

Number

e201812297

Issue

2

Start page

1

End page

12

Total pages

12

Publisher

Rockefeller University Press

Place published

United States

Language

English

Copyright

© 2020 Lynagh et al.

Former Identifier

2006097351

Esploro creation date

2023-04-28

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