Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration.

Tao Su,Hen Meng,Meng-Long Chen,Bin Tang,Xiao-Rong Liu,Wei-Ping Liao,Li-Hong Liu

doi:10.3389/fnmol.2021.797628

Abstract

Objective: An overwhelming majority of the genetic variants associated with genetic disorders are missense. The association between the nature of substitution and the functional alteration, which is critical in determining the pathogenicity of variants, remains largely unknown. With a novel missense variant (E1623A) identified from two epileptic cases, which occurs in the extracellular S3-S4 loop of Nav1.1, we studied functional changes of all latent mutations at residue E1623, aiming to understand the relationship between substitution nature and functional alteration.Methods: Six latent mutants with amino acid substitutions at E1623 were generated, followed by measurements of their electrophysiological alterations. Different computational analyses were used to parameterize the residue alterations.Results: Structural modeling indicated that the E1623 was located in the peripheral region far from the central pore, and contributed to the tight turn of the S3-S4 loop. The E1623 residue exhibited low functional tolerance to the substitutions with the most remarkable loss-of-function found in E1623A, including reduced current density, less steady-state availability of activation and inactivation, and slower recovery from fast inactivation. Correlation analysis between electrophysiological parameters and the parameterized physicochemical properties of different residues suggested that hydrophilicity of side-chain at E1623 might be a crucial contributor for voltage-dependent kinetics. However, none of the established algorithms on the physicochemical variations of residues could well predict changes in the channel conductance property indicated by peak current density.Significance: The results established the important role of the extracellular S3-S4 loop in Nav1.1 channel gating and proposed a possible effect of local conformational loop flexibility on channel conductance and kinetics. Site-specific knowledge of protein will be a fundamental task for future bioinformatics.

Highlights

The distinct function of a protein depends on the well-organized composition of the amino acids and intricate folding of the molecule
An SCN1A variant c.4868A>C/p.E1623A was identified from two cases of epilepsy, including a case with de novo variant and a familial case with three individuals affected (Figures 1A–C)
The variant occurs in exon 26 of SCN1A and leads to the substitution of glutamic acid by alanine at E1623 that locates in the extracellular loop linking S3-S4 in DIV of Nav1.1 (Figures 1D,E)

Summary

Introduction

The distinct function of a protein depends on the well-organized composition of the amino acids and intricate folding of the molecule. In contrast to destructive mutations that result in remarkably damaging effects on protein composition, the functional consequence of missense mutations is far more unpredictable. Our previous study demonstrated that the molecular sub-regional location of the variant plays a critical in determining the damaging effect of the mutations (Tang et al, 2020). The pathogenicity or functional impact of a missense mutation depends on its location and potentially on the nature of amino acid substituted, such as molecular mass, polarity, and acidity. The association between the nature of substitution and the functional alteration, which remains largely unknown, is a critical aspect in exploring the molecular mechanism underlying the pathogenicity of variants

Methods

Results

Conclusion