Cargando…
Structure-function and rational design of a spider toxin Ssp1a at human voltage-gated sodium channel subtypes
The structure-function and optimization studies of Na(V)-inhibiting spider toxins have focused on developing selective inhibitors for peripheral pain-sensing Na(V)1.7. With several Na(V) subtypes emerging as potential therapeutic targets, structure-function analysis of Na(V)-inhibiting spider toxins...
Autores principales: | Dongol, Yashad, Wilson, David T., Daly, Norelle L., Cardoso, Fernanda C., Lewis, Richard J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682951/ https://www.ncbi.nlm.nih.gov/pubmed/38034993 http://dx.doi.org/10.3389/fphar.2023.1277143 |
Ejemplares similares
-
Voltage-Gated Sodium Channel Modulation by a New Spider Toxin Ssp1a Isolated From an Australian Theraphosid
por: Dongol, Yashad, et al.
Publicado: (2021) -
Spider Knottin Pharmacology at Voltage-Gated Sodium Channels and Their Potential to Modulate Pain Pathways
por: Dongol, Yashad, et al.
Publicado: (2019) -
Molecular basis of the interaction between gating modifier spider toxins and the voltage sensor of voltage-gated ion channels
por: Lau, Carus H. Y., et al.
Publicado: (2016) -
Shellfish Toxins Targeting Voltage-Gated Sodium Channels
por: Zhang, Fan, et al.
Publicado: (2013) -
Marine Toxins That Target Voltage-gated Sodium Channels
por: Al-Sabi, Ahmed, et al.
Publicado: (2006)