Article
Computational Design of High-Affinity Blockers for Sodium Channel NaV1.2 from μ-Conotoxin KIIIA.
Marine drugs - 21 Feb 2022
Meng Guangsi, Kuyucak Serdar
Abstract excerpt
The voltage-gated sodium channel subtype 1.2 (NaV1.2) is instrumental in the initiation of action potentials in the nervous system, making it a natural drug target for neurological diseases. Therefore, there is much pharmacological interest in finding blockers of NaV1.2 and improving their affinity and selectivity properties. An extensive family of peptide toxins from cone snails (conotoxins) block NaV channels,...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
