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Structure of human Na V 1.6 channel reveals Na + selectivity and pore blockade by 4,9-anhydro-tetrodotoxin.

Yue LiTian YuanBo HuangFeng ZhouChao PengXiaojing LiYunlong QiuBei YangYan ZhaoZhuo HuangDaohua Jiang
Published in: Nature communications (2023)
The sodium channel Na V 1.6 is widely expressed in neurons of the central and peripheral nervous systems, which plays a critical role in regulating neuronal excitability. Dysfunction of Na V 1.6 has been linked to epileptic encephalopathy, intellectual disability and movement disorders. Here we present cryo-EM structures of human Na V 1.6/β1/β2 alone and complexed with a guanidinium neurotoxin 4,9-anhydro-tetrodotoxin (4,9-ah-TTX), revealing molecular mechanism of Na V 1.6 inhibition by the blocker. The apo-form structure reveals two potential Na + binding sites within the selectivity filter, suggesting a possible mechanism for Na + selectivity and conductance. In the 4,9-ah-TTX bound structure, 4,9-ah-TTX binds to a pocket similar to the tetrodotoxin (TTX) binding site, which occupies the Na + binding sites and completely blocks the channel. Molecular dynamics simulation results show that subtle conformational differences in the selectivity filter affect the affinity of TTX analogues. Taken together, our results provide important insights into Na V 1.6 structure, ion conductance, and inhibition.
Keyphrases
  • intellectual disability
  • molecular dynamics simulations
  • endothelial cells
  • autism spectrum disorder
  • high resolution
  • brain injury
  • structural basis
  • induced pluripotent stem cells