Journal article
A conserved energetic footprint underpins recognition of human leukocyte antigen-E by two distinct αβ T cell receptors
LC Sullivan, NG Walpole, C Farenc, G Pietra, MJW Sum, CS Clements, EJ Lee, T Beddoe, M Falco, MC Mingari, L Moretta, S Gras, J Rossjohn, AG Brooks
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2017
Abstract
αβ T cell receptors (TCRs) interact with peptides bound to the polymorphic major histocompatibility complex class Ia (MHC-Ia) and class II (MHC-II) molecules as well as the essentially monomorphic MHC class Ib (MHC-Ib) molecules. Although there is a large amount of information on how TCRs engage with MHC-Ia and MHC-II, our understanding of TCR/ MHC-Ib interactions is very limited. Infection with cytomegalovirus (CMV) can elicit a CD8Tcell response restricted by the human MHC-Ib molecule human leukocyte antigen (HLA)-E and specific for an epitope from UL40 (VMAPRTLIL), which is characterized by biased TRBV14 gene usage. Here we describe an HLA-E-restricted CD8+ T cell able to recognize an all..
View full abstract