Evidence map›Paper›PMID 33023980›Full record

ArticleMolecular & cellular proteomics : MCP2020

Spatially Resolved Activity-based Proteomic Profiles of the Murine Small Intestinal Lipases.

Matthias Schittmayer, Nemanja Vujic, Barbara Darnhofer, Melanie Korbelius, Sophie Honeder, Dagmar Kratky, Ruth Birner-Gruenberger

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Treatment with saponins fromNutrition research and practice · 2026
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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

7 authors at 2 institutions in 1 country.

Matthias SchittmayerInstitute of Chemical Technologies and Analytics, Vienna University of Technology, Vienna, Austria; Diagnostic and Research Institute of Pathology, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria. Electronic address: matthias.schittmayer@tuwien.ac.at.
Nemanja VujicGottfried Schatz Research Center, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Barbara DarnhoferDiagnostic and Research Institute of Pathology, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Melanie KorbeliusGottfried Schatz Research Center, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Sophie HonederDiagnostic and Research Institute of Pathology, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Dagmar KratkyGottfried Schatz Research Center, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria. Electronic address: dagmar.kratky@medunigraz.at.
Ruth Birner-GruenbergerInstitute of Chemical Technologies and Analytics, Vienna University of Technology, Vienna, Austria; Diagnostic and Research Institute of Pathology, Medical University Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria. Electronic address: ruth.birner-gruenberger@tuwien.ac.at.
Medical University of Graz · ATTU Wien · AT

Funding

Austrian Science Fund FWF P 30882Austrian Science Fund FWF W 1226
6 · The paper itself

Abstract

Despite the crucial function of the small intestine in nutrient uptake our understanding of the molecular events underlying the digestive function is still rudimentary. Recent studies demonstrated that enterocytes do not direct the entire dietary triacylglycerol toward immediate chylomicron synthesis. Especially after high-fat challenges, parts of the resynthesized triacylglycerol are packaged into cytosolic lipid droplets for transient storage in the endothelial layer of the small intestine. The reason for this temporary storage of triacylglycerol is not completely understood. To utilize lipids from cytosolic lipid droplets for chylomicron synthesis in the endoplasmic reticulum, stored triacylglycerol has to be hydrolyzed either by cytosolic lipolysis or lipophagy. Interestingly, triacylglycerol storage and chylomicron secretion rates are unevenly distributed along the small intestine, with the proximal jejunum exhibiting the highest intermittent storage capacity. We hypothesize that correlating hydrolytic enzyme activities with the reported distribution of triacylglycerol storage and chylomicron secretion in different sections of the small intestine is a promising strategy to determine key enzymes in triacylglycerol remobilization. We employed a serine hydrolase specific activity-based labeling approach in combination with quantitative proteomics to identify and rank hydrolases based on their relative activity in 11 sections of the small intestine. Moreover, we identified several clusters of enzymes showing similar activity distribution along the small intestine. Merging our activity-based results with substrate specificity and subcellular localization known from previous studies, carboxylesterase 2e and arylacetamide deacetylase emerge as promising candidates for triacylglycerol mobilization from cytosolic lipid droplets in enterocytes.

Indexed as

ProteomicsAnimalsHydrolasesIntestine, SmallLipaseMaleMice, Inbred C57BLHydrolasesLipaseactivity based proteomicslabel-free quantificationlipid dropletmass spectrometrymechanism of actionmolecular probesmouse modelssmall intestine

Identifiers

PMID33023980
PMCPMC7710144
OpenAlexW3092364882

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.