3UTP
1E6 TCR specific for HLA-A*0201-ALWGPDPAAA
Summary for 3UTP
Entry DOI | 10.2210/pdb3utp/pdb |
Related | 3UTQ 3UTS 3UTT |
Descriptor | 1E6 TCR alpha chain, 1E6 TCR beta chain, GLYCEROL, ... (6 entities in total) |
Functional Keywords | t cell receptor, type i diabetes, immune system |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 4 |
Total formula weight | 102536.99 |
Authors | Rizkallah, P.J.,Cole, D.K.,Sewell, A.K.,Bulek, A.M. (deposition date: 2011-11-26, release date: 2012-01-25, Last modification date: 2024-11-27) |
Primary citation | Bulek, A.M.,Cole, D.K.,Skowera, A.,Dolton, G.,Gras, S.,Madura, F.,Fuller, A.,Miles, J.J.,Gostick, E.,Price, D.A.,Drijfhout, J.W.,Knight, R.R.,Huang, G.C.,Lissin, N.,Molloy, P.E.,Wooldridge, L.,Jakobsen, B.K.,Rossjohn, J.,Peakman, M.,Rizkallah, P.J.,Sewell, A.K. Structural basis for the killing of human beta cells by CD8(+) T cells in type 1 diabetes. Nat.Immunol., 13:283-289, 2012 Cited by PubMed Abstract: The structural characteristics of the engagement of major histocompatibility complex (MHC) class II-restricted self antigens by autoreactive T cell antigen receptors (TCRs) is established, but how autoimmune TCRs interact with complexes of self peptide and MHC class I has been unclear. Here we examined how CD8(+) T cells kill human islet beta cells in type 1 diabetes via recognition of a human leukocyte antigen HLA-A*0201-restricted glucose-sensitive preproinsulin peptide by the autoreactive TCR 1E6. Rigid 'lock-and-key' binding underpinned the 1E6-HLA-A*0201-peptide interaction, whereby 1E6 docked similarly to most MHC class I-restricted TCRs. However, this interaction was extraordinarily weak because of limited contacts with MHC class I. TCR binding was highly peptide centric, dominated by two residues of the complementarity-determining region 3 (CDR3) loops that acted as an 'aromatic-cap' over the complex of peptide and MHC class I (pMHCI). Thus, highly focused peptide-centric interactions associated with suboptimal TCR-pMHCI binding affinities might lead to thymic escape and potential CD8(+) T cell-mediated autoreactivity. PubMed: 22245737DOI: 10.1038/ni.2206 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.574 Å) |
Structure validation
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