OxTalks will soon move to the new Halo platform and will become 'Oxford Events.' There will be a need for an OxTalks freeze. This was previously planned for Friday 14th November – a new date will be shared as soon as it is available (full details will be available on the Staff Gateway).
In the meantime, the OxTalks site will remain active and events will continue to be published.
If staff have any questions about the Oxford Events launch, please contact halo@digital.ox.ac.uk
The T cell receptor (TCR) plays an important role in the immune system by recognizing peptide antigens presented by the major histocompatibility complex (MHC). Despite decades of research, the TCR remains enigmatic, as it is not clear how binding of an immunogenic peptide-MHC complex (pMHC) is signaled over the plasma membrane. The TCR lacks a cytoplasmic domain, but forms a complex with the CD3 proteins, which have long cytoplasmic tails that contain the ITAM motifs, which are phosphorylated upon TCR-pMHC binding. It has been conceptually difficult to understand how extracellular TCR-pMHC binding results in the phosphorylation of the ITAMs inside the cell; the TCR lacks a proper cytoplasmic domain, while the CD3 proteins are too short to interact with the pMHC. The fact that the TCR and CD3 associate non-covalently further complicates the problem. Based upon extensive molecular dynamics simulations, we present an allosteric mechanism for TCR triggering upon pMHC binding for which we obtained experimental support.
van Eerden Floris J., Sherif Aalaa Alrahman, Llamas-Covarrubias Mara Anais, Millius Arthur, Lu Xiuyuan, Ishizuka Shigenari, Yamasaki Sho, Standley Daron M. (2023) TCR-pMHC complex formation triggers CD3 dynamics eLife 12:RP88065
