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Molecular determinants of resurgent sodium currents mediated by NavĪ²4 peptide and A-type FHFs.

Authors :
Yucheng Xiao
Yanling Pan
Jingyu Xiao
Cummins, Theodore R.
Source :
Frontiers in Molecular Neuroscience; 2024, p1-14, 14p
Publication Year :
2024

Abstract

Introduction: Resurgent current (INaR) generated by voltage-gated sodium channels (VGSCs) plays an essential role in maintaining high-frequency firing of many neurons and contributes to disease pathophysiology such as epilepsy and painful disorders. Targeting INaR may present a highly promising strategy in the treatment of these diseases. Navß4 and A-type fibroblast growth factor homologous factors (FHFs) have been identified as two classes of important INaR mediators; however, their receptor sites in VGSCs remain unknown, which hinders the development of novel agents to effectively target INaR. Methods: Navß4 and FHF4A can mediate INaR generation through the amino acid segment located in their C-terminus and N-terminus, respectively. We mainly employed site-directed mutagenesis, chimera construction and wholecell patch-clamp recording to explore the receptor sites of Navß4 peptide and FHF4A in Nav1.7 and Nav1.8. Results: We show that the receptor of Navß4-peptide involves four residues, N395, N945, F1737 and Y1744, in Nav1.7 DI-S6, DII-S6, and DIV-S6. We show that A-type FHFs generating INaR depends on the segment located at the very beginning, not at the distal end, of the FHF4 N-terminus domain. We show that the receptor site of A-type FHFs also resides in VGSC inner pore region. We further show that an asparagine at DIIS6, N891 in Nav1.8, is a major determinant of INaR generated by A-type FHFs in VGSCs. Discussion: Cryo-EM structures reveal that the side chains of the critical residues project into the VGSC channel pore. Our findings provide additional evidence that Navß4 peptide and A-type FHFs function as open-channel pore blockers and highlight channel inner pore region as a hotspot for development of novel agents targeting INaR. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16625099
Database :
Complementary Index
Journal :
Frontiers in Molecular Neuroscience
Publication Type :
Academic Journal
Accession number :
180354058
Full Text :
https://doi.org/10.3389/fnmol.2024.1433981