An Antigen Produced by Splicing of Noncontiguous Peptides in the Reverse Order

Author:

Warren Edus H.12345,Vigneron Nathalie J.12345,Gavin Marc A.12345,Coulie Pierre G.12345,Stroobant Vincent12345,Dalet Alexandre12345,Tykodi Scott S.12345,Xuereb Suzanne M.12345,Mito Jeffrey K.12345,Riddell Stanley R.12345,Van den Eynde Benoît J.12345

Affiliation:

1. Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

2. Department of Medicine, University of Washington, Seattle, WA 98195, USA.

3. Department of Immunology, University of Washington, Seattle, WA 98195, USA.

4. Ludwig Institute for Cancer Research, Brussels Branch, B-1200 Brussels, Belgium.

5. Cellular Genetics Unit, Institute of Cellular Pathology, Université Catholique de Louvain, B-1200 Brussels, Belgium.

Abstract

CD8-positive T lymphocytes recognize peptides that are usually derived from the degradation of cellular proteins and are presented by class I molecules of the major histocompatibility complex. Here we describe a human minor histocompatibility antigen created by a polymorphism in the SP110 nuclear phosphoprotein gene. The antigenic peptide comprises two noncontiguous SP110 peptide segments spliced together in reverse order to that in which they occur in the predicted SP110 protein. The antigenic peptide could be produced in vitro by incubation of precursor peptides with highly purified 20 S proteasomes. Cutting and splicing probably occur within the proteasome by transpeptidation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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