Evidence map›Paper›PMID 21387142›Full record

ReviewCellular and molecular life sciences : CMLS2011

Insights into MHC class I antigen processing gained from large-scale analysis of class I ligands.

Gabor Mester, Vanessa Hoffmann, Stefan Stevanović

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Protein networks and activation of lymphocytes.Current opinion in immunology · 2015
    Review
  12. Article
  13. Review
  14. Article
  15. Expanding the detectable HLA peptide repertoire using electron-transfer/higher-energy collision dissociation (EThcD).Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  16. Article
  17. Dipeptides promote folding and peptide binding of MHC class I molecules.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  18. Article
  19. The human leukocyte antigen-presented ligandome of B lymphocytes.Molecular & cellular proteomics : MCP · 2013
    Article
  20. Bioinformatics for cancer immunology and immunotherapy.Cancer immunology, immunotherapy : CII · 2012
    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

3 authors.

Gabor MesterInstitute for Cell Biology, Department of Immunology, Eberhard Karls University Tübingen, Tübingen, Germany.
Vanessa Hoffmann
Stefan Stevanović

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Short peptides derived from intracellular proteins and presented on MHC class I molecules on the cell surface serve as a showcase for the immune system to detect pathogenic or malignant alterations inside the cell, and the sequencing and analysis of the presented peptide pool has received considerable attention over the last two decades. In this review, we give a comprehensive presentation of the methods employed for the large-scale qualitative and quantitative analysis of the MHC class I ligandome. Furthermore, we focus on insights gained into the underlying processing pathway, especially involving the roles of the proteasome, the TAP complex, and the peptide specificities and motifs of MHC molecules. The identification of post-translational modifications in MHC ligands and their implications for processing are also considered. Finally, we review the correlations of the ligandome to the proteome and the transcriptome.

Indexed as

AnimalsAntigen PresentationHistocompatibility Antigens Class IHumansImmunity, CellularLigandsMiceProteasome Endopeptidase ComplexProtein Processing, Post-TranslationalHistocompatibility Antigens Class ILigandsProteasome Endopeptidase Complex

Identifiers

PMID21387142
PMCPMC11114492

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.