Computational Design of High-Affinity Blockers for Sodium Channel NaV1.2 from μ-Conotoxin KIIIA

The voltage-gated sodium channel subtype 1.2 (Na(V)1.2) 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 Na(V)1.2 and improving their affinity and selectivity properties. An extensive family of peptide toxins from cone snails (conotoxins) block Na-V channels, thus they provide natural templates for the design of drugs targeting Na-V channels. Unfortunately, progress was hampered due to the absence of any Na-V structures. The recent determination of cryo-EM structures for Na-V channels has finally broken this impasse. Here, we use the Na(V)1.2 structure in complex with mu-conotoxin KIIIA (KIIIA) in computational studies with the aim of improving KIIIA's affinity and blocking capacity for Na(V)1.2. Only three KIIIA amino acid residues are available for mutation (S5, S6, and S13). After performing molecular modeling and simulations on Na(V)1.2-KIIIA complex, we have identified the S5R, S6D, and S13K mutations as the most promising for additional contacts. We estimate these contacts to boost the affinity of KIIIA for Na(V)1.2 from nanomole to picomole domain. Moreover, the KIIIA[S5R, S6D, S13K] analogue makes contacts with all four channel domains, thus enabling the complete blocking of the channel (KIIIA partially blocks as it has contacts with three domains). The proposed KIIIA analogue, once confirmed experimentally, may lead to novel anti-epileptic drugs.

Automated summary

This study aims to improve the affinity and blocking capacity of mu-conotoxin KIIIA for Na(V)1.2 through computational studies. After molecular modeling and simulations on the Na(V)1.2-KIIIA complex, the S5R, S6D, and S13K mutations were identified as the most promising for additional contacts, which could enhance the affinity of KIIIA for Na(V)1.2 and enable complete blocking of the channel.