6DFQ

mouse diabetogenic TCR I.29

6DFQ の概要

• エントリーDOI: 10.2210/pdb6dfq/pdb
• 分子名称: TCR alpha chain, TCR beta chain, CALCIUM ION, ... (5 entities in total)
• 機能のキーワード: t cell receptor, type 1 diabetes, autoimmunity, immune system
• 由来する生物種: Mus musculus; 詳細
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 204833.14

構造登録者

Wang, Y.,Dai, S. (登録日: 2018-05-15, 公開日: 2019-04-17, 最終更新日: 2024-10-09)

主引用文献

Wang, Y.,Sosinowski, T.,Novikov, A.,Crawford, F.,White, J.,Jin, N.,Liu, Z.,Zou, J.,Neau, D.,Davidson, H.W.,Nakayama, M.,Kwok, W.W.,Gapin, L.,Marrack, P.,Kappler, J.W.,Dai, S.
How C-terminal additions to insulin B-chain fragments create superagonists for T cells in mouse and human type 1 diabetes.
Sci Immunol, 4:-, 2019

PubMed Abstract: In type 1 diabetes (T1D), proinsulin is a major autoantigen and the insulin B:9-23 peptide contains epitopes for CD4 T cells in both mice and humans. This peptide requires carboxyl-terminal mutations for uniform binding in the proper position within the mouse IA or human DQ8 major histocompatibility complex (MHC) class II (MHCII) peptide grooves and for strong CD4 T cell stimulation. Here, we present crystal structures showing how these mutations control CD4 T cell receptor (TCR) binding to these MHCII-peptide complexes. Our data reveal stricking similarities between mouse and human CD4 TCRs in their interactions with these ligands. We also show how fusions between fragments of B:9-23 and of proinsulin C-peptide create chimeric peptides with activities as strong or stronger than the mutated insulin peptides. We propose transpeptidation in the lysosome as a mechanism that could accomplish these fusions in vivo, similar to the creation of fused peptide epitopes for MHCI presentation shown to occur by transpeptidation in the proteasome. Were this mechanism limited to the pancreas and absent in the thymus, it could provide an explanation for how diabetogenic T cells escape negative selection during development but find their modified target antigens in the pancreas to cause T1D.

PubMed: 30952805
DOI: 10.1126/sciimmunol.aav7517

実験手法

X-RAY DIFFRACTION (2.6 Å)