Glycan side chains on naturally presented MHC class II ligands

被引:31
作者
Dengjel, J [1 ]
Rammensee, HG [1 ]
Stevanovic, S [1 ]
机构
[1] Univ Tubingen, Inst Cell Biol, Dept Immunol, D-72076 Tubingen, Germany
来源
JOURNAL OF MASS SPECTROMETRY | 2005年 / 40卷 / 01期
关键词
glycopeptide; MHC class II ligand; N-linked glycan; in-source fragmentation; electrospray mass spectrometry;
D O I
10.1002/jms.780
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. Copyright (C) 2005 John Wiley Sons, Ltd.
引用
收藏
页码:100 / 104
页数:5
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