# Structure-function analysis of the lithium-ion selectivity of the voltage-gated sodium channel

**Authors:** Yuki K. Maeda, Kentaro Kojima, Tomoe Y. Nakamura, Toru Nakatsu, Katsumasa Irie

PMC · DOI: 10.1085/jgp.202513855 · The Journal of General Physiology · 2026-02-19

## TL;DR

This paper identifies the molecular basis for lithium ion selectivity in sodium channels, which could lead to new treatments for neurological disorders.

## Contribution

The study introduces the first prokaryotic sodium channel mutant with higher lithium selectivity than sodium.

## Key findings

- A prokaryotic Nav mutant conducts Li+ twice as efficiently as Na+.
- Electrophysiological and crystallographic analyses reveal atomic determinants for Li+ permeation.
- Strong electrostatic interactions and fewer hydration water exchanges enhance Li+ selectivity.

## Abstract

Navs exhibit high Li+ selectivity similar to Na+. We present the first prokaryotic Nav mutant that conducts Li+ with approximately twice the efficiency of Na+. Electrophysiological and crystallographic analyses suggest atomic determinants that facilitate Li+ permeation through the ion pore.

Voltage-gated sodium channels (Navs) selectively conduct Na+ to generate action potentials. Na+ permeates Navs with significantly higher efficiency than many other cations, but Li+ can also permeate Navs to an extent comparable with Na+. Li+ in the blood is known to enter cells via Navs and to have a beneficial effect on various neuropathies. However, the molecular basis of the high Li+ selectivity of Navs was unclear. In this study, using a prokaryotic Nav, we successfully created the first Nav mutant to be more selective for Li+ than for Na+. Electrophysiological and crystallographic analyses suggested the critical determinants of high Li+ selectivity: the strong electrostatic interaction between the ion pathway and hydrated ions, and the smaller number of hydration water exchanges within the ion pathway. Additionally, the extensive interactions around the ion pathway were shown to support monovalent cation selectivity. New drug directions based on the molecular basis for Li+ permeation may target various neurological disorders and could clarify the broader biological effects of lithium.

## Linked entities

- **Chemicals:** Li+ (PubChem CID 28486), Na+ (PubChem CID 923)

## Full-text entities

- **Genes:** CAV2 (caveolin 2) [NCBI Gene 858] {aka CAV}, BCL2A1 (BCL2 related protein A1) [NCBI Gene 597] {aka ACC-1, ACC-2, ACC1, ACC2, BCL2L5, BFL1}, SCN1A (sodium voltage-gated channel alpha subunit 1) [NCBI Gene 6323] {aka DEE6, DEE6A, DEE6B, DRVT, EIEE6, FEB3}, SCN5A (sodium voltage-gated channel alpha subunit 5) [NCBI Gene 6331] {aka CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD}, SCN10A (sodium voltage-gated channel alpha subunit 10) [NCBI Gene 6336] {aka FEPS2, Nav1.8, PN3, SNS}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, KLHDC2 (kelch domain containing 2) [NCBI Gene 23588] {aka HCLP-1, HCLP1, LCP}, SCN3A (sodium voltage-gated channel alpha subunit 3) [NCBI Gene 6328] {aka DEE62, EIEE62, FFEVF4, NAC3, Nav1.3}
- **Diseases:** neurological disorders (MESH:D009461), fetal diseases (MESH:D005315), Alzheimer's disease (MESH:D000544), neurological, immune, and cardiovascular disorders (MESH:D020274), mitochondrial dysfunction (MESH:D028361), neuropathies (MESH:D009422), bipolar disorder (MESH:D001714), depressive (MESH:D003866), toxicity (MESH:D064420)
- **Chemicals:** asparagine (MESH:D001216), NaOH (MESH:D012972), CaCl2 (MESH:D002122), Li (MESH:D008094), Cation (MESH:D002412), NaF (MESH:D012969), imidazole (MESH:C029899), water (MESH:D014867), cadmium nitrate (MESH:C035196), PNa (MESH:D020135), magnesium nitrate (MESH:C018330), carbon (MESH:D002244), DDM (MESH:C117975), n-dodecyl-beta-D-maltoside (MESH:C040358), HIS (MESH:D006639), oxygen (MESH:D010100), PLi (MESH:C044850), NaCl (MESH:D012965), glucose (MESH:D005947), DMSO (MESH:D004121), Ca (MESH:D002118), polyethylene glycol monomethyl ether (MESH:C028210), LiCl (MESH:D018021), hydrogen (MESH:D006859), LiOH (MESH:C028467), Cs (MESH:D002586), EGTA (MESH:D004533), Cobalt (MESH:D003035), glutamine (MESH:D005973), Ser (MESH:D012694), aspartate (MESH:D001224), rhamnose (MESH:D012210), K (MESH:D011188), Na+ (MESH:D012964), HEPES (MESH:D006531), 1,2-dimyristoyl-sn-glycero-3-phosphorylcholine (-), calcium nitrate (MESH:C059948)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** S178ANK/TA, Q172N, S178A, S178T, glycine to serine, T206A, N49K, S178G, Gln172, Met181, Ser178, S178TNK/TA, M181A
- **Cell lines:** SF-9 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_RG56), insect — Trichoplusia ni (Cabbage looper), Spontaneously immortalized cell line (CVCL_C190)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12919392/full.md

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12919392/full.md

## References

76 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919392/full.md

---
Source: https://tomesphere.com/paper/PMC12919392