Evidence map›Paper›PMID 42875621›Full record

ArticleEMBO reports2026

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

Aamna Jain, Alexander von der Malsburg, Cynthia Alsayyah, Claudia Götz, Mohamed Elmofty, John Reinhard, Per Haberkant, Volkhard Helms, Joseph H Lorent, Robert Ernst

Abstract read
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Article in EMBO reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Aamna JainMedical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany.ORCID http://orcid.org/0009-0003-7536-7026
Alexander von der MalsburgMedical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany.ORCID http://orcid.org/0000-0002-7412-2276
Cynthia AlsayyahMedical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany.ORCID http://orcid.org/0000-0003-1714-031X
Claudia GötzMedical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany.ORCID http://orcid.org/0000-0001-7115-0485
Mohamed ElmoftyPharmaScienceHub (PSH), Saarland University, Saarbrücken, Germany.ORCID http://orcid.org/0009-0005-1193-7995
John ReinhardMedical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany.ORCID http://orcid.org/0000-0001-6363-2994
Per HaberkantEMBL Heidelberg, Proteomics Core Facility, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-5608-9062
Volkhard HelmsPharmaScienceHub (PSH), Saarland University, Saarbrücken, Germany.ORCID http://orcid.org/0000-0002-2180-9154
Joseph H LorentCellular and Molecular Pharmacology (FACM), Louvain Drug Research Institute, UCLouvain, Avenue Mounier 73/1, B-1200, Brussels, Belgium.ORCID http://orcid.org/0000-0002-7537-8521
Robert ErnstMedical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany. robert.ernst@uni-saarland.de.ORCID http://orcid.org/0000-0002-0283-3490

Funding

Deutsche Forschungsgemeinschaft (DFG) EXC-3094 - 533751785EC | European Research Council (ERC) 866011)
6 · The paper itself

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.

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.