Mammalian MemPrep establishes the lipid composition of ER membranes in HEK293T cells

The endoplasmic reticulum (ER) forms a dynamic network of sheets and tubules, whose 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 ER membranes are dominated by phosphatidylcholine and monounsaturated glycerophospholipids, consistent with a highly compressible bilayer. Although proteomics suggests a functional specialization of ER tubules and an enrichment of tubule-associated proteins, 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 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 suggests that membrane properties are maintained across the ER.

Authors

Institutions

Publication Details

Journal
EMBO Reports
Published
2026-10-14
DOI
https://doi.org/10.1038/s44319-026-00952-9
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mammalian MemPrep establishes the lipid composition of ER membranes in HEK293T cells

Cynthia Alsayyah, Robert Ernst, Joseph Helmuth Lorent, Aamna Jain et al.
EMBO Reports
Lipid Membrane Structure and Behavior
article

Mammalian MemPrep establishes the lipid composition of ER membranes in HEK293T cells

Cynthia Alsayyah, Robert Ernst, Joseph Helmuth Lorent, Aamna Jain, John F. Reinhard, Alexander von der Malsburg, Volkhard Helms, Per Haberkant, Claudia Götz, Mohamed Elmofty
article en

Abstract

The endoplasmic reticulum (ER) forms a dynamic network of sheets and tubules, whose 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 ER membranes are dominated by phosphatidylcholine and monounsaturated glycerophospholipids, consistent with a highly compressible bilayer. Although proteomics suggests a functional specialization of ER tubules and an enrichment of tubule-associated proteins, 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 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 suggests that membrane properties are maintained across the ER.

EMBO Reports
Goethe University Frankfurt (DE), Max Perutz Labs (AT), European Molecular Biology Laboratory (DE), Saarland University (DE), UCLouvain (BE)
European Commission, Deutsche Forschungsgemeinschaft, European Research Council
Openalex Percentile: Top 24%
Lipid Membrane Structure and Behavior
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.