| Literature DB >> 28923982 |
Nishant K Singh1,2, Timothy P Riley1,2, Sarah Catherine B Baker1,2, Tyler Borrman3, Zhiping Weng3, Brian M Baker4,2.
Abstract
T cell specificity emerges from a myriad of processes, ranging from the biological pathways that control T cell signaling to the structural and physical mechanisms that influence how TCRs bind peptides and MHC proteins. Of these processes, the binding specificity of the TCR is a key component. However, TCR specificity is enigmatic: TCRs are at once specific but also cross-reactive. Although long appreciated, this duality continues to puzzle immunologists and has implications for the development of TCR-based therapeutics. In this review, we discuss TCR specificity, emphasizing results that have emerged from structural and physical studies of TCR binding. We show how the TCR specificity/cross-reactivity duality can be rationalized from structural and biophysical principles. There is excellent agreement between predictions from these principles and classic predictions about the scope of TCR cross-reactivity. We demonstrate how these same principles can also explain amino acid preferences in immunogenic epitopes and highlight opportunities for structural considerations in predictive immunology.Entities:
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Year: 2017 PMID: 28923982 PMCID: PMC5679125 DOI: 10.4049/jimmunol.1700744
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422