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PMID: 15643650 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Glycan side chains on naturally presented MHC class II ligands.

Journal of mass spectrometry : JMS ·Vol. 40 ·No. 1 ·2005-01-00 ·Pages 100-4

Dengjel J, Rammensee HG, Stevanovic S

Abstract

The molecular characterization of unknown naturally presented major histocompatibility complex (MHC) class II glycopeptides carrying complex glycans has so far not been achieved, reflecting the different fragmentation characteristics of sugars and peptides in mass spectrometric analysis. Human leukocyte antigen (HLA)-DR-bound peptides were isolated by affinity purification, separated via high performance liquid chromatography and analyzed by matrix-assisted laser desorption/ionization and electrospray ionization mass spectrometry. We were able to identify two naturally processed MHC class II ligands, CD53(122-136) and CD53(121-136), carrying complex N-linked glycan side chains by a combination of in-source and collision-induced fragmentation on a quadrupole time-of-flight tandem mass spectrometer.

MeSH Terms
Glycosylation HLA Antigens/analysis Histocompatibility Antigens Class II/analysis Humans Ligands Polysaccharides/analysis Spectrometry, Mass, Electrospray Ionization/methods Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods
Chemicals
HLA Antigens Histocompatibility Antigens Class II Ligands Polysaccharides
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dengjel Jörn
Department of Immunology, Institute for Cell Biology, University of Tübingen, 72076 Tübingen, Germany.
Rammensee Hans-Georg
Stevanovic Stefan
Article Info
Journal
Journal of mass spectrometry : JMS
Abbr.
J Mass Spectrom
ISSN
1076-5174
Published
2005-01-00
Pages
100-4
Language
English
Region
England
NLM ID
9504818
Subset
IM
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