Evidence map›Paper›PMID 21913724›Full record

ArticleJournal of proteome research2011

Mass spectrometry analysis and quantitation of peptides presented on the MHC II molecules of mouse spleen dendritic cells.

Leonia Bozzacco, Haiqiang Yu, Henry A Zebroski, Jörn Dengjel, Haiteng Deng, Svetlana Mojsov, Ralph M Steinman

Abstract read
In one paragraph

Article in Journal of proteome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

36 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  4. Immunoproteomics: The Evolution from Classical Methods to Emerging Techniques.Methods in molecular biology (Clifton, N.J.) · 2026
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  11. Absolute quantification of tumor antigens using embedded MHC-I isotopologue calibrants.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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 2 countries.

Leonia BozzaccoThe Rockefeller University, New York, NY 10065-6399, USA. lbozzacco@rockefeller.edu
Haiqiang Yu
Henry A Zebroski
Jörn Dengjel
Haiteng Deng
Svetlana Mojsov
Ralph M Steinman
Rockefeller University · USUniversity of Freiburg · DE

Funding

The role of src-family protein kinases in dendritic cell physiologyP01AI051573 · NIAID · ROCKEFELLER UNIVERSITY · PI RAVETCH, JEFFREY VICTOR · 2002 to 2011
$18.3M
Properties of Mouse of Dendritic Cells and MacrophagesR01AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI MOJSOV, SVETLANA · 1985 to 2015
$8.9M
PROPERTIES OF MOUSE DENDRITIC CELLS AND MACROPHAGESR37AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1986 to 1995
–
NIAID NIH HHS AI051573NIAID NIH HHS AI13013NIAID NIH HHS P01 AI051573NIAID NIH HHS R01 AI013013
6 · The paper itself

Abstract

Major histocompatibility complex class II (MHC II) molecules are expressed on the surface of antigen-presenting cells and display short bound peptide fragments derived from self- and nonself antigens. These peptide-MHC complexes function to maintain immunological tolerance in the case of self-antigens and initiate the CD4(+) T cell response in the case of foreign proteins. Here we report the application of LC-MS/MS analysis to identify MHC II peptides derived from endogenous proteins expressed in freshly isolated murine splenic DCs. The cell number was enriched in vivo upon treatment with Flt3L-B16 melanoma cells. In a typical experiment, starting with about 5 × 10(8) splenic DCs, we were able to reliably identify a repertoire of over 100 MHC II peptides originating from about 55 proteins localized in membrane (23%), intracellular (26%), endolysosomal (12%), nuclear (14%), and extracellular (25%) compartments. Using synthetic isotopically labeled peptides corresponding to the sequences of representative bound MHC II peptides, we quantified by LC-MS relative peptide abundance. In a single experiment, peptides were detected in a wide concentration range spanning from 2.5 fmol/μL to 12 pmol/μL or from approximately 13 to 2 × 10(5) copies per DC. These peptides were found in similar amounts on B cells where we detected about 80 peptides originating from 55 proteins distributed homogenously within the same cellular compartments as in DCs. About 90 different binding motifs predicted by the epitope prediction algorithm were found within the sequences of the identified MHC II peptides. These results set a foundation for future studies to quantitatively investigate the MHC II repertoire on DCs generated under different immunization conditions.

Indexed as

Antigen PresentationAlgorithmsAmino Acid SequenceAnimalsB-LymphocytesCell Line, TumorDendritic CellsHistocompatibility Antigens Class IIMiceMice, Inbred BALB CMice, Inbred C57BLMolecular Sequence DataNeoplasm TransplantationPeptide FragmentsPrimary Cell CultureSpleenHistocompatibility Antigens Class IIPeptide Fragments

Identifiers

PMID21913724
PMCPMC3270889
OpenAlexW2052084314

What OpenQuestion holds

Textmetadata
LicenceTDM
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.