Evidence map›Paper›PMID 20613855›Full record

ArticlePLoS computational biology2010

The 20S proteasome splicing activity discovered by SpliceMet.

Juliane Liepe, Michele Mishto, Kathrin Textoris-Taube, Katharina Janek, Christin Keller, Petra Henklein, Peter Michael Kloetzel, Alexey Zaikin

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

37 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. T-Cell Receptor Repertoire Sequencing in the Era of Cancer Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  3. Article
  4. Sources of Cancer Neoantigens beyond Single-Nucleotide Variants.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Neo-Splicetopes in Tumor Therapy: A Lost Case?Frontiers in immunology · 2022
    Review
  8. Article
  9. Spliced HLA-bound peptides: a Black Swan event in immunology.Clinical and experimental immunology · 2021
    Review
  10. Article
  11. Article
  12. Response: Commentary: AnFrontiers in immunology · 2021
    Article
  13. Are There Indeed Spliced Peptides in the Immunopeptidome?Molecular & cellular proteomics : MCP · 2021
    Article
  14. Article
  15. Review
  16. Proteolytic dynamics of human 20S thymoproteasome.The Journal of biological chemistry · 2019
    Article
  17. Article
  18. AnFrontiers in immunology · 2019
    Article
  19. Article
  20. Islet stress, degradation and autoimmunity.Diabetes, obesity & metabolism · 2018
    Review
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

8 authors at 2 institutions in 3 countries.

Juliane LiepeInstitut für Biochemie, Charité, Universitätsmedizin Berlin, Berlin, Germany.
Michele Mishto
Kathrin Textoris-Taube
Katharina Janek
Christin Keller
Petra Henklein
Peter Michael Kloetzel
Alexey Zaikin
Charité - Universitätsmedizin Berlin · DEUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of proteasome-generated spliced peptides (PSP) revealed a new unpredicted activity of the major cellular protease. However, so far characterization of PSP was entirely dependent on the availability of patient-derived cytotoxic CD8+ T lymphocytes (CTL) thus preventing a systematic investigation of proteasome-catalyzed peptide splicing (PCPS). For an unrestricted PSP identification we here developed SpliceMet, combining the computer-based algorithm ProteaJ with in vitro proteasomal degradation assays and mass spectrometry. By applying SpliceMet for the analysis of proteasomal processing products of four different substrate polypeptides, derived from human tumor as well as viral antigens, we identified fifteen new spliced peptides generated by PCPS either by cis or from two separate substrate molecules, i.e., by trans splicing. Our data suggest that 20S proteasomes represent a molecular machine that, due to its catalytic and structural properties, facilitates the generation of spliced peptides, thereby providing a pool of qualitatively new peptides from which functionally relevant products may be selected.

Indexed as

AlgorithmsSoftwareAmino Acid SequenceAntigens, NuclearAutoantigensCD8-Positive T-LymphocytesComputational BiologyComputer SimulationDatabases, ProteinEpitopes, T-LymphocyteFibroblast Growth Factor 5gp100 Melanoma AntigenHumansMembrane GlycoproteinsMolecular Sequence DataPeptide FragmentsAntigens, NuclearAutoantigensEpitopes, T-LymphocyteFGF5 protein, humanFibroblast Growth Factor 5gp100 Melanoma AntigenMembrane GlycoproteinsPeptide FragmentsPMEL protein, humanProteasome Endopeptidase ComplexSP100 protein, human

Identifiers

PMID20613855
PMCPMC2891702
OpenAlexW2045715135

What OpenQuestion 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 OpenQuestion graph.