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PMID: 1546328 Published · ppublish English Comment Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Characterization of peptides bound to the class I MHC molecule HLA-A2.1 by mass spectrometry.

Science (New York, N.Y.) ·Vol. 255 ·No. 5049 ·1992-03-06 ·Pages 1261-3

Hunt DF, Henderson RA, Shabanowitz J, Sakaguchi K, Michel H, Sevilir N, Cox AL, Appella E, Engelhard VH

Abstract

Antigens recognized by T cells are expressed as peptides bound to major histocompatibility complex (MHC) molecules. Microcapillary high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry was used to fractionate and sequence subpicomolar amounts of peptides isolated from the MHC molecule HLA-A2.1. Of 200 different species quantitated, eight were sequenced and four were found in cellular proteins. All were nine residues long and shared a distinct structural motif. The sensitivity and speed of this approach should enhance the analysis of peptides from small quantities of virally infected and transformed cells as well as those associated with autoimmune disease states.

MeSH Terms
Amino Acid Sequence Antigens/chemistry,immunology,metabolism Cell Line Chromatography, High Pressure Liquid HLA-A2 Antigen/metabolism Humans Immunosorbent Techniques Mass Spectrometry Molecular Sequence Data Peptides/chemistry,immunology,metabolism T-Lymphocytes/immunology
Chemicals
Antigens HLA-A2 Antigen Peptides
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Hunt D F
Department of Chemistry, University of Virginia, Charlottesville 22903.
Henderson R A
Shabanowitz J
Sakaguchi K
Michel H
Sevilir N
Cox A L
Appella E
Engelhard V H
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1992-03-06
Pages
1261-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIAID NIH HHS · AI20963 · United States
NIGMS NIH HHS · GM37537 · United States
Corrections
CommentOn
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