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Pre–T cell receptors topologically sample self-ligands during thymocyte β-selection
Author(s) -
Xiaolong Li,
Réka Mizsei,
Kemin Tan,
Robert J. Mallis,
Jonathan S. DukeCohan,
Aoi Akitsu,
Paul W. Tetteh,
Abhinav Dubey,
Wonmuk Hwang,
Gerhard Wagner,
Matthew J. Lang,
Haribabu Arthanari,
JiaHuai Wang,
Ellis L. Reinherz
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abe0918
Subject(s) - complementarity determining region , t cell receptor , major histocompatibility complex , complementarity (molecular biology) , t cell , thymocyte , receptor , computational biology , biology , microbiology and biotechnology , immunoglobulin light chain , antigen , immune system , immunology , genetics , antibody
PreTCRs use horizontal docking geometry The T cell receptor (TCR) recognizes peptide-bound major histocompatibility complex molecules (pMHCs) and consists of an α chain in association with a β chain. Both chains have hypervariable complementarity-determining regions (CDRs) that inform whether a particular TCR can recognize a given pMHC. To successfully graduate from the thymus, aspiring αβT cells must generate a functional TCR. During one early checkpoint in this process, the β chain is first paired with a preTβ chain to form the preTCR. Liet al. used x-ray crystallography to visualize how preTCRs recognize pMHCs. They report that the CDR3 loop of the preTCR β chain contacts the pMHC with a distinctive lateral topography. This is in contrast to the established binding modality of mature TCRs, whereby all three CDR loops on both α and β chains bind in a vertical orientation. These complexes help solve the mystery of how only functionally rearranged β chains using competent CDR3 loops can properly engage with pMHC at the preTCR stage.Science , this issue p.181

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