Characterization of Peptides Bound to the Class I MHC Molecule HLA-A2.1 by Mass Spectrometry

Donald F. Hunt(University of Virginia), Robert Henderson(Carter Center), Jeffrey Shabanowitz(University of Virginia), Kazuyasu Sakaguchi(National Cancer Institute), Hanspeter Michel(University of Virginia), Noelle Sevilir(Carter Center), Andrea L. Cox(University of Virginia), Ettore Appella(National Cancer Institute), Víctor H. Engelhard(Carter Center)
Science
March 6, 1992
Cited by 1,205Open Access

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.


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