Asymmetric membrane properties through a protein lens

Abstract

Plasma membranes are asymmetric, with each monolayer presenting specific lipid compositions and biophysical properties. Transmembrane domains (TMDs) of single-pass transmembrane proteins (spTMP) have adapted their physico-chemical properties to these asymmetric constraints. In this study we analysed structural features of such TMDs across the tree of life to obtain information about their interaction with asymmetric membrane bilayers and predict species-specific membrane properties. We observed that TMDs in the plasma membranes of all eukaryotic species possess asymmetries in lipid accessible surface area (ASA), hydrophobicity, aromaticity and charge. Bacteria deviate from this trend, with strong differences between bacterial clades. Notably, TMDs in the Golgi and the endoplasmic reticulum of eukaryotic species display inverted profiles for accessible surface area, hydrophobicity and aromaticity compared to their plasma membrane counterparts. To determine how well TMD profiles reflect average membrane properties, we performed molecular dynamics simulations of a spTMP in a asymmetric lipid bilayer whose composition approximates the human plasma membrane. The simulated spTMP was chosen to represent the average TMD properties of the human proteome. We compared the electron density profiles of the simulated asymmetric membrane to the average TMD profiles derived from the human proteome and observed that phospholipid acyl chain density overlapped very well with TMD hydrophobicity, and phosphate groups with TMD charge. The profiles of phospholipid unsaturations in acyl chains overlapped well with the average location of TMD phenylalanines in the cytoplasmic leaflet, while there was additional accumulation of large hydrophobic and aromatic residues in the membrane midplane, which had low acyl chain density. This study reveals complementarity of membrane and TMD properties in asymmetric membranes, suggesting that the properties of TMDs can be used to make predictions about the properties of their solvating membranes.

Supplementary files

Article information

Article type
Paper
Submitted
15 Dec 2024
Accepted
03 Feb 2025
First published
04 Feb 2025

Faraday Discuss., 2024, Accepted Manuscript

Asymmetric membrane properties through a protein lens

J. H. Lorent, A. Cabrera-Jojo, K. Levental, I. Levental and E. Lyman, Faraday Discuss., 2024, Accepted Manuscript , DOI: 10.1039/D4FD00199K

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