Evidence map›Paper›PMID 36416088›Full record

ArticleAutophagy2023

FACS-mediated isolation of native autophagic vesicles.

Daniel Schmitt, Süleyman Bozkurt, Pascale Henning-Domres, Heike Huesmann, Stefan Eimer, Laura Bindila, Christian Behrends, Emily Boyle, Florian Wilfling, Georg Tascher and 3 more

Abstract read
In one paragraph

Article in Autophagy, 2023. 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
–field-weighted citation impact
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

13 authors.

Daniel SchmittInstitute of Pathobiochemistry, The Autophagy Lab, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Süleyman BozkurtInstitute of Biochemistry II, Faculty of Medicine, Goethe University, Frankfurt am Main, Germany.
Pascale Henning-DomresInstitute of Pathobiochemistry, The Autophagy Lab, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Heike HuesmannInstitute of Pathobiochemistry, The Autophagy Lab, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Stefan EimerDepartment of Structural Cell Biology, Institute for Cell Biology and Neuroscience, Goethe University, Frankfurt am Main, Germany.
Laura BindilaInstitute of Physiological Chemistry, Clinical Lipidomics Unit, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Christian BehrendsMunich Cluster for Systems Neurology (SyNergy), Ludwig-Maximilians- University, Munich, Germany.
Emily BoyleMechanisms of Cellular Quality Control, Max Planck Institute of Biophysics, Frankfurt am Main, Germany.
Florian WilflingMechanisms of Cellular Quality Control, Max Planck Institute of Biophysics, Frankfurt am Main, Germany.
Georg TascherInstitute of Biochemistry II, Faculty of Medicine, Goethe University, Frankfurt am Main, Germany.
Christian MünchInstitute of Biochemistry II, Faculty of Medicine, Goethe University, Frankfurt am Main, Germany.
Christian BehlInstitute of Pathobiochemistry, The Autophagy Lab, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Andreas KernInstitute of Pathobiochemistry, The Autophagy Lab, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagosome isolation enables the thorough investigation of structural components and engulfed materials. Recently, we introduced a novel antibody-based FACS-mediated method for isolation of native macroautophagic/autophagic vesicles and confirmed the quality of the preparations. We performed phospholipidomic and proteomic analyses to characterize autophagic vesicle-associated phospholipids and protein cargoes under different autophagy conditions. Lipidomic analyses identified phosphoglycerides and sphingomyelins within autophagic vesicles and revealed that the lipid composition was unaffected by different rates of autophagosome formation. Proteomic analyses identified more than 4500 potential autophagy substrates and showed that in comparison to autophagic vesicles isolated under basal autophagy conditions, starvation only marginally affected the cargo profile. Proteasome inhibition, however, resulted in the enhanced degradation of ubiquitin-proteasome system components. Taken together, the novel isolation method enriched large quantities of autophagic vesicles and enabled detailed analyses of their lipid and cargo composition.

Indexed as

AutophagyProteasome Endopeptidase ComplexAutophagosomesLipidsProteomicsLipidsProteasome Endopeptidase ComplexAutophagic vesiclesautophagycargo profilinglipid profilingvesicle isolation

Identifiers

PMID36416088
PMCPMC10283435

What OpenQuestion holds

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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 OpenQuestion graph.