A structural atlas of druggable sites on Na_v channels

ABSTRACT

Voltage-gated sodium (Na_v) channels govern membrane excitability by initiating and propagating action potentials. Consistent with their physiological significance, dysfunction, or mutations in these channels are associated with various channelopathies. Na_v channels are thereby major targets for various clinical and investigational drugs. In addition, a large number of natural toxins, both small molecules and peptides, can bind to Na_v channels and modulate their functions. Technological breakthrough in cryo-electron microscopy (cryo-EM) has enabled the determination of high-resolution structures of eukaryotic and eventually human Na_v channels, alone or in complex with auxiliary subunits, toxins, and drugs. These studies have not only advanced our comprehension of channel architecture and working mechanisms but also afforded unprecedented clarity to the molecular basis for the binding and mechanism of action (MOA) of prototypical drugs and toxins. In this review, we will provide an overview of the recent advances in structural pharmacology of Na_v channels, encompassing the structural map for ligand binding on Na_v channels. These findings have established a vital groundwork for future drug development.

KEYWORDS:

• Na_v channels
• structural pharmacology
• mode of action (MOA)
• analgesics
• anti-epilepsy drugs (AED)

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

Data sharing is not applicable to this article as no new data were created or analyzed in this study.

Additional information

Funding

This work was funded by the National Natural Science Foundation of China (Project 32330052).