8VQ8
Immune receptor complex
Summary for 8VQ8
Entry DOI | 10.2210/pdb8vq8/pdb |
Descriptor | T cell receptor - LCK1-1 TRAV6-5 alpha chain, T cell receptor - LCK1-1 TRBV1 Beta chain, H-2 class II histocompatibility antigen, A-B alpha chain, ... (7 entities in total) |
Functional Keywords | peptide hla complex, immune system-viral peptide complex, immune system |
Biological source | Mus musculus More |
Total number of polymer chains | 4 |
Total formula weight | 99318.50 |
Authors | Chaurasia, P.,Littler, D.R.,La Gruta, N.,Rossjohn, J. (deposition date: 2024-01-17, release date: 2025-01-29, Last modification date: 2025-08-13) |
Primary citation | Zhang, J.B.,Chaurasia, P.,Nguyen, A.,Huang, Z.,Nguyen, T.T.,Xu, H.,Tran, M.T.,Reid, H.H.,Jones, C.M.,Schattgen, S.A.,Thiele, D.,Thomas, P.G.,Rientjes, J.,Good-Jacobson, K.L.,Ruscher, R.,Littler, D.R.,Rossjohn, J.,Zareie, P.,La Gruta, N.L. LCK-co-receptor association ensures T cell lineage fidelity and maximizes epitope-specific TCR diversity. Sci Immunol, 10:eadp5016-eadp5016, 2025 Cited by PubMed Abstract: The interaction between the CD4/CD8 co-receptors and LCK (an Src family tyrosine kinase) is thought to augment T cell activation upon recognition of peptide-loaded major histocompatibility complexes (pMHCs). How this interaction influences antigen-specific T cell development is unclear however, as is its impact on naïve and immune antigen-specific T cell repertoires. In mice expressing mutated endogenous LCK unable to bind co-receptors (LCK mice), we show that influenza A virus (IAV)-derived pMHC-specific CD8 and CD4 T cell responses had a significantly narrowed T cell receptor (TCR) repertoire, favoring high-affinity TCRs. This narrowing was established during T cell development and was exacerbated after viral infection. The dissociation of LCK from co-receptors also resulted in the redirection of CD4-fated T cells to the CD8 lineage, with expanded pMHCII-specific cytotoxic CD8 T cells observed after IAV infection. Thus, LCK-co-receptor association is critical for ensuring T cell lineage fidelity and maximizing antigen-specific T cell repertoire diversity. PubMed: 39982976DOI: 10.1126/sciimmunol.adp5016 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.01 Å) |
Structure validation
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