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An antigenic peptide produced by peptide splicing in the proteasome
Authors:Vigneron Nathalie  Stroobant Vincent  Chapiro Jacques  Ooms Annie  Degiovanni Gérard  Morel Sandra  van der Bruggen Pierre  Boon Thierry  Van den Eynde Benoît J
Affiliation:Ludwig Institute for Cancer Research and Cellular Genetics Unit, Université de Louvain, B-1200 Brussels, Belgium.
Abstract:CD8 T lymphocytes recognize peptides of 8 to 10 amino acids presented by class I molecules of the major histocompatibility complex. Here, CD8 T lymphocytes were found to recognize a nonameric peptide on melanoma cells that comprises two noncontiguous segments of melanocytic glycoprotein gp100(PMEL17). The production of this peptide involves the excision of four amino acids and splicing of the fragments. This process was reproduced in vitro by incubating a precursor peptide of 13 amino acids with highly purified proteasomes. Splicing appears to occur by transpeptidation involving an acyl-enzyme intermediate. Our results reveal an unanticipated aspect of the proteasome function of producing antigenic peptides.
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