TY - JOUR
T1 - MHC class II tetramers made from isolated recombinant α and β chains refolded with affinity-tagged peptides
AU - Braendstrup, Peter
AU - Justesen, Sune Frederik Lamdahl
AU - Osterbye, Thomas
AU - Nielsen, Lise Lotte Bruun
AU - Mallone, Roberto
AU - Vindeløv, Lars
AU - Stryhn, Anette
AU - Buus, Søren
PY - 2013
Y1 - 2013
N2 - Targeting CD4+ T cells through their unique antigen-specific, MHC class II-restricted T cell receptor makes MHC class II tetramers an attractive strategy to identify, validate and manipulate these cells at the single cell level. Currently, generating class II tetramers is a specialized undertaking effectively limiting their use and emphasizing the need for improved methods of production. Using class II chains expressed individually in E. coli as versatile recombinant reagents, we have previously generated peptide-MHC class II monomers, but failed to generate functional class II tetramers. Adding a monomer purification principle based upon affinity-tagged peptides, we here provide a robust method to produce class II tetramers and demonstrate staining of antigen-specific CD4+ T cells. We also provide evidence that both MHC class II and T cell receptor molecules largely accept affinity-tagged peptides. As a general approach to class II tetramer generation, this method should support rational CD4+ T cell epitope discovery as well as enable specific monitoring and manipulation of CD4+ T cell responses.
AB - Targeting CD4+ T cells through their unique antigen-specific, MHC class II-restricted T cell receptor makes MHC class II tetramers an attractive strategy to identify, validate and manipulate these cells at the single cell level. Currently, generating class II tetramers is a specialized undertaking effectively limiting their use and emphasizing the need for improved methods of production. Using class II chains expressed individually in E. coli as versatile recombinant reagents, we have previously generated peptide-MHC class II monomers, but failed to generate functional class II tetramers. Adding a monomer purification principle based upon affinity-tagged peptides, we here provide a robust method to produce class II tetramers and demonstrate staining of antigen-specific CD4+ T cells. We also provide evidence that both MHC class II and T cell receptor molecules largely accept affinity-tagged peptides. As a general approach to class II tetramer generation, this method should support rational CD4+ T cell epitope discovery as well as enable specific monitoring and manipulation of CD4+ T cell responses.
U2 - 10.1371/journal.pone.0073648
DO - 10.1371/journal.pone.0073648
M3 - Journal article
C2 - 24023895
SN - 1932-6203
VL - 8
SP - e73648
JO - P L o S One
JF - P L o S One
IS - 9
ER -