# Membrane Depth Measurements of E Protein by 2H ESEEM Spectroscopy in Lipid Bilayers

## TL;DR

This study uses ESEEM spectroscopy to determine how the E protein from SARS-CoV-2 interacts with lipid bilayers at different depths.

## Contribution

The paper provides new membrane depth measurements for the E protein using 2H ESEEM spectroscopy.

## Key findings

- Spin labels on the transmembrane helix of E protein show close contact with lipid acyl chains and solvent.
- The C-terminal domain shows lower lipid acyl chain contact but similar solvent exposure.
- The C-terminal domain is likely in contact with the bilayer surface.

## Abstract

A topological analysis was performed by taking ESEEM measurements of site-specifically labeled E protein from SARS-CoV-2. The intensity of deuterium modulation arising from either deuterated solvent or deuterated lipid acyl chains revealed exposure to solvent or the bilayer hydrophobic region. Spin-labeled lipids and soluble spin labels were used as points of comparison. The data indicate that spin labels placed along the transmembrane helix of the E protein showed close contact with lipid acyl chains, but also substantial contact with solvent, while those placed on the C-terminal domain showed substantial but lower exposure to lipid acyl chains, with comparable solvent exposure. The results support the view that the C-terminal domain is in contact with the bilayer surface.