Generation of peptide-MHC class I complexes through UV-mediated ligand exchange

Boris Rodenko, Mireille Toebes, Sine Reker Hadrup, Wim J. E. van Esch, Annemieke M. Molenaar, Ton N. M. Schumacher, Huib Ovaa

Research output: Contribution to journalJournal articleResearchpeer-review


Major histocompatibility complex (MHC) class I molecules present peptide ligands on the cell surface for recognition by appropriate cytotoxic T cells. MHC-bound peptides are critical for the stability of the MHC complex, and standard strategies for the production of recombinant MHC complexes are based on in vitro refolding reactions with specific peptides. This strategy is not amenable to high-throughput production of vast collections of MHC molecules. We have developed conditional MHC ligands that form stable complexes with MHC molecules but can be cleaved upon UV irradiation. The resulting empty, peptide-receptive MHC molecules can be charged with epitopes of choice under native conditions. Here we describe in-depth procedures for the high-throughput production of peptide-MHC (pMHC) complexes by MHC exchange, the analysis of peptide exchange efficiency by ELISA and the parallel production of MHC tetramers for T-cell detection. The production of the conditional pMHC complex by an in vitro refolding reaction can be achieved within 2 weeks, and the actual high-throughput MHC peptide exchange and subsequent MHC tetramer formation require less than a day.
Original languageEnglish
JournalNature Protocols (Online)
Issue number3
Pages (from-to)1120-1132
Number of pages13
Publication statusPublished - 2006
Externally publishedYes


  • Biochemistry, Genetics and Molecular Biology (all)
  • ligand
  • multiprotein complex
  • peptide
  • article
  • chemical structure
  • enzyme linked immunosorbent assay
  • gene
  • genetics
  • metabolism
  • methodology
  • protein folding
  • synthesis
  • ultraviolet radiation
  • Enzyme-Linked Immunosorbent Assay
  • Genes, MHC Class I
  • Ligands
  • Molecular Structure
  • Multiprotein Complexes
  • Peptides
  • Protein Folding
  • Ultraviolet Rays
  • CELL

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