Structural Modeling of Peptide Toxin - Ion Channel Interactions using RosettaDock
Abstract
SUMMARYVoltage-gated ion channels play essential physiological roles in action potential generation and propagation. Peptidic toxins from animal venoms target ion channels and provide useful scaffolds for the rational design of novel channel modulators with enhanced potency and subtype selectivity. Despite recent progress in obtaining experimental structures of peptide toxin - ion channel complexes, structural determination of peptide toxins bound to ion channels in physiologically important states remains challenging. Here we describe an application of RosettaDock approach to structural modeling of peptide toxins interactions with ion channels. We tested this approach on 10 structures of peptide toxinion channel complexes and demonstrated that it can sample near-native structures in all tested cases. Our approach will be useful for improving understanding of the molecular mechanism of natural peptide toxin modulation of ion channel gating and for the structural modeling of novel peptide-based ion channel modulators.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Towards high-resolution modeling of small molecule-ion channel interactions
Brandon J Harris, Phuong T. Nguyen, … Vladimir M. Yarov-Yarovoy·Frontiers in PharmacologyPeer-reviewed·Jun 11, 2024
- Elucidating Molecular Mechanisms of Protoxin-2 State-specific Binding to the Human NaV1.7 Channel
K. Ngo, D. L. Mateos, … I. Vorobyov·bioRxiv·Feb 27, 2023
- Molecular Determinants of μ-Conotoxin KIIIA interaction with the Voltage-Gated Sodium Channel Nav1.7
I. H. Kimball, P. T. Nguyen, … V. Yarov-Yarovoy·bioRxiv·Feb 2, 2023
- Structural basis of inhibition of human NaV1.8 by the tarantula venom peptide Protoxin-I
Bryan Neumann, Stephen McCarthy, Shane Gonen·Nature CommunicationsPeer-reviewed·Feb 7, 2025
- Pore-modulating toxins exploit inherent slow inactivation to block K+ channels
I. Karbat, H. Altman-Gueta, … E. Reuveny·bioRxiv·Mar 13, 2019
- Evaluating the ligands' potency to modulate the fast inactivation of voltage-gated sodium channel.
Beata Niklas, Milena Jankowska, … Wiesław Nowak·International Journal of Biological MacromoleculesPeer-reviewed·Nov 20, 2025