Effect of CDR3 sequences and distal V gene residues in regulating TCR-MHC contacts and ligand specificity.

ABSTRACT: The mature T cell repertoire has the ability to orchestrate immunity to a wide range of potential pathogen challenges. This ability stems from thymic development producing individual T cell clonotypes that express TCRs with unique patterns of Ag reactivity. The Ag specificity of TCRs is created from the combinatorial pairing of one of a set of germline encoded TCR Vα and Vβ gene segments with randomly created CDR3 sequences. How the amalgamation of germline encoded and randomly created TCR sequences results in Ag receptors with unique patterns of ligand specificity is not fully understood. Using cellular, biophysical, and structural analyses, we show that CDR3α residues can modulate the geometry in which TCRs bind peptide-MHC (pMHC), governing whether and how germline encoded TCR Vα and Vβ

SUBMITTER: Stadinski BD 

PROVIDER: S-EPMC4097884 | biostudies-literature | 2014 Jun

REPOSITORIES: biostudies-literature