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3UTP

1E6 TCR specific for HLA-A*0201-ALWGPDPAAA

Summary for 3UTP
Entry DOI10.2210/pdb3utp/pdb
Related3UTQ 3UTS 3UTT
Descriptor1E6 TCR alpha chain, 1E6 TCR beta chain, GLYCEROL, ... (6 entities in total)
Functional Keywordst cell receptor, type i diabetes, immune system
Biological sourceHomo sapiens (human)
More
Total number of polymer chains4
Total formula weight102536.99
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 citationBulek, 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: 22245737
DOI: 10.1038/ni.2206
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.574 Å)
Structure validation

237735

数据于2025-06-18公开中

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