# How Sodium and Calcium Ions Pass Through Batrachotoxin-Bound Sodium Channel

**Authors:** Boris S. Zhorov

PMC · DOI: 10.3390/toxins17100520 · Toxins · 2025-10-21

## TL;DR

This study explains how batrachotoxin changes the way sodium and calcium ions move through sodium channels, increasing calcium permeation.

## Contribution

The study reveals a novel mechanism of ion permeation in batrachotoxin-bound sodium channels using computational modeling.

## Key findings

- Deprotonated nitrogen in the toxin and DEKA lysine allows ion passage through the channel.
- Electrostatic interactions with BTX-B stabilize the 'dunked' lysine conformation, reducing calcium attraction.
- The DEKA lysine alternates between protonated and deprotonated states during ion permeation.

## Abstract

Steroidal sodium channel agonist batrachotoxin (BTX), one of the most potent animal toxins, dramatically increases calcium permeation and alters other channel characteristics. In a cryoEM structure of rat sodium channel Nav1.5 with two BTX-B molecules, one toxin binds between repeats III and IV and exposes to the pore lumen two oxygen atoms and protonatable nitrogen. The mechanism of ion permeation and selectivity in BTX-bound channel is unclear. Here Monte Carlo energy-minimized profiles of sodium and calcium ions pulled through the pore were computed in models with various protonated states of the DEKA lysine and BTX-B. The only model where the ions readily passed by the DEKA lysine and BTX-B involved their deprotonated nitrogens. In this model, electronegative atoms of BTX-B attracted a permeant cation that stabilized the “dunked” lysine through electrostatic interactions and nearby water molecules. This would retard reprotonation of the lysine and its “uplifting” to the DEKA carboxylates, which otherwise attracts calcium. The results suggest how sodium and calcium ions pass through BTX-bound sodium channel and why BTX increases calcium permeation. The study supports an earlier hypothesis that during the sodium ion permeation cycle, the DEKA lysine alternates between uplifted and dunked conformations in the protonated and deprotonated states, respectively, while the sodium-displaced proton and the sodium ion nullify the net electrical charge at the DEKA region.

## Linked entities

- **Genes:** SCN5A (sodium voltage-gated channel alpha subunit 5) [NCBI Gene 6331]
- **Chemicals:** batrachotoxin (PubChem CID 6324647), calcium ions (PubChem CID 271)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Scn5a (sodium voltage-gated channel alpha subunit 5) [NCBI Gene 25665] {aka Nav1.5, RATRSKM2X, RSKM2X, SCAL, Scn2x, rSkM2}
- **Chemicals:** water (MESH:D014867), oxygen (MESH:D010100), Sodium (MESH:D012964), DEKA (-), lysine (MESH:D008239), nitrogen (MESH:D009584), Calcium (MESH:D002118)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12567824/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12567824/full.md

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Source: https://tomesphere.com/paper/PMC12567824