Structural biology of γδ T cell receptors
T cell receptor (TCR) diversity underpins cellular immunity. While αβ TCRs have been extensively studied in the context of major histocompatibility complex (MHC)-restricted antigen recognition, the γδ TCR system remains underexplored. Unlike their αβ counterparts, γδ TCRs display versatile, often MHC-independent recognition modes, engaging diverse ligands ranging from butyrophilins (BTNs) and other disparate molecules. Recent advances in cryo-electron microscopy (cryo-EM) paired with crystallographic data have illuminated critical aspects of γδ TCR -ligand interactions, the CD3 complex architecture, and the inherent flexibility underpinning their varied recognition modes. In this review, we compare the classical αβ TCR-MHC paradigm against the backdrop of emerging γδ TCR structures, highlighting the latest cryo-EM findings and their implications for immunobiology.
Authors
- Michael T. Rice (ORCID: https://orcid.org/0000-0002-2693-0252)
- Liam Rashleigh (ORCID: https://orcid.org/0009-0008-7271-229X)
- Mengqi Pan
- Jamie Rossjohn
Institutions
- Australian Regenerative Medicine Institute (AU)
- Institute of Infection and Immunity (CA)
- Monash University (AU)
Publication Details
- Journal
- Current Opinion in Structural Biology
- Published
- 2026-02-12
- DOI
- https://doi.org/10.1016/j.sbi.2026.103221
- Primary Topic
- T-cell and B-cell Immunology
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Health and Medical Research Council