HA(306-318) is an immunodominant peptide of the hemagglutinin of influenza virus that binds to most human leukocyte antigen (HLA-DR) alleles, while p18(73-85) is a HIV peptide characterized as a DR101 binding peptide. Our results demonstrate that crystal relaxation leads to the loss of a hydrogen bond between the beta81 histidine and the HA(306-318) peptide. This histidine is also involved in the binding of superantigens like SEA via a coordination of a zinc atom. To monitor the interaction of these peptides with this histidine of HLA-DR molecules, chemical modification, peptide binding on HLA-DR101 wild type and mutated molecules, and proliferation experiments were conducted, together with molecular simulation of HLA-DR/peptide molecular complexes. Our data suggest a different binding peptide pattern, depending of whether the peptide is HLA-DR101 allele specific or a shared one. Furthermore, tyrosine substitution at position beta81 does not affect either peptide binding or HA(306-318) clone-specific T-cell proliferation. On the contrary, the alanine substitution at position HLA-DR101 beta81 abrogated both peptide binding and T-cell proliferation. These results suggest that the histidine 81 on the DRbeta chain plays an important role in the HLA-DR peptide binding, more likely by polar interactions of the amino acid side chain ring with the peptide.
Antigen Presentation , HLA-DR Antigens/chemistry , HLA-DR Antigens/metabolism , Histidine/metabolism , Peptides/immunology , Receptors, Antigen, T-Cell/immunology , Animals , Binding Sites , Cells, Cultured , HLA-DR Antigens/genetics , Histidine/genetics , Humans , Lymphocyte Activation , Mice , Models, Molecular , Peptides/metabolism , Protein Binding , Receptors, Antigen, T-Cell/metabolism , T-Lymphocytes/classification , T-Lymphocytes/metabolism
