Mammalian MemPrep establishes the lipid composition of ER membranes in HEK293T cells
Aamna JainiD, Alexander von der MalsburgiD, Cynthia AlsayyahiD, Claudia GötziD, Mohamed ElmoftyiD, John F. ReinhardiD, Per HaberkantiD, Volkhard HelmsiD, Joseph Helmuth LorentiD, Robert ErnstiD
Abstract
The endoplasmic reticulum (ER) forms a dynamic network of sheets and tubules, whose molecular lipid composition remains incompletely defined. Using an optimized MemPrep workflow, we establish a high-confidence lipidome of the mammalian ER and selectively enrich membrane vesicles originating from ER tubules as a major ER subdomain. Quantitative lipidomics show that ER membranes are dominated by phosphatidylcholine and mono-unsaturated glycerophospholipids, consistent with a highly compressible bilayer. Although proteomics suggests a functional specialization of ER tubules and an enrichment of tubule-associated proteins therein, the lipidome of an ER tubule-enriched isolate is indistinguishable from the general ER, indicating that principal ER architectures share a common lipid composition. Integration of lipidomic data with bioinformatic analyses of transmembrane helices further demonstrates that the physicochemical features of ER lipids mirror those of ER-resident membrane proteins, including reduced hydrophobicity and increased polarity compared to plasma membrane proteins. These findings support a coordinated evolution of ER proteins and lipids based on shared biophysical constraints. Together, this work provides a definitive characterization of the mammalian ER lipidome and suggest that membrane properties are maintained across the entire ER.
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