1. Academic Validation
  2. FGF14 Peptide Derivative Differentially Regulates Nav1.2 and Nav1.6 Function

FGF14 Peptide Derivative Differentially Regulates Nav1.2 and Nav1.6 Function

  • Life (Basel). 2025 Aug 25;15(9):1345. doi: 10.3390/life15091345.
Parsa Arman 1 Zahra Haghighijoo 1 Carmen A Lupascu 2 Aditya K Singh 1 Nana A Goode 1 Timothy J Baumgartner 1 Jully Singh 1 Yu Xue 1 Pingyuan Wang 1 Haiying Chen 1 Dinler A Antunes 3 Marijn Lijffijt 4 Jia Zhou 1 Michele Migliore 2 Fernanda Laezza 1 4
Affiliations

Affiliations

  • 1 Department of Pharmacology & Toxicology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, USA.
  • 2 Institute of Biophysics, National Research Council, 90146 Palermo, Italy.
  • 3 Department of Biology and Biochemistry, University of Houston, Houston, TX 77004, USA.
  • 4 IonTX Inc., Friendswood, TX 77546, USA.
Abstract

Voltage-gated Na+ channels (Nav) are the molecular determinants of action potential initiation and propagation. Among the nine voltage-gated Na+ channel isoforms (Nav1.1-Nav1.9), Nav1.2 and Nav1.6 are of particular interest because of their developmental expression profile throughout the central nervous system (CNS) and their association with channelopathies. Although the α-subunit coded by each of the nine isoforms can sufficiently confer transient Na+ currents (INa), in vivo these channels are modulated by auxiliary proteins like intracellular Fibroblast Growth Factor (iFGFs) through protein-protein interaction (PPI), and probes developed from iFGF/Nav PPI complexes have been shown to precisely modulate Nav channels. Previous studies identified ZL0177, a peptidomimetic derived from a short peptide sequence at the FGF14/Nav1.6 PPI interface, as a functional modulator of Nav1.6-mediated INa+. However, the isoform specificity, binding sites, and putative physiological impact of ZL0177 on neuronal excitability remain unexplored. Here, we used automated planar patch-clamp electrophysiology to assess ZL0177's functional activity in cells stably expressing Nav1.2 or Nav1.6. While ZL0177 was found to suppress INa in both Nav1.2- and Nav1.6-expressing cells, ZL0177 elicited functionally divergent effects on channel kinetics that were isoform-specific and supported by differential docking of the compound to AlphaFold structures of the two channel isoforms. Computational modeling predicts that ZL0177 modulates Nav1.2 and Nav1.6 in an isoform-specific manner, eliciting phenotypically divergent effects on action potential discharge. Taken together, these results highlight the potential of PPI derivatives for isoform-specific regulation of Nav channels and the development of therapeutics for channelopathies.

Keywords

FGF14; Nav1.2; Nav1.6; automated planar patch electrophysiology; central nervous system (CNS); drug discovery; protein–protein interaction (PPI); voltage-gated Na+ channel (Nav).

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