Pre–T cell receptors topologically sample self-ligands during thymocyte β-selection

Author:

Li Xiaolong123ORCID,Mizsei Réka1ORCID,Tan Kemin4ORCID,Mallis Robert J.156ORCID,Duke-Cohan Jonathan S.123ORCID,Akitsu Aoi123ORCID,Tetteh Paul W.12ORCID,Dubey Abhinav67ORCID,Hwang Wonmuk891011ORCID,Wagner Gerhard6ORCID,Lang Matthew J.1213ORCID,Arthanari Haribabu67ORCID,Wang Jia-huai126714ORCID,Reinherz Ellis L.123ORCID

Affiliation:

1. Laboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA, USA.

2. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

3. Department of Medicine, Harvard Medical School, Boston, MA, USA.

4. Structural Biology Center, X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Lemont, IL, USA.

5. Department of Dermatology, Harvard Medical School, Boston, MA, USA.

6. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.

7. Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, USA.

8. Department of Biomedical Engineering, Texas A&M University, College Station, TX, USA.

9. Department of Materials Science & Engineering, Texas A&M University, College Station, TX, USA.

10. Department of Physics & Astronomy, Texas A&M University, College Station, TX, USA.

11. School of Computational Sciences, Korea Institute for Advanced Study, Seoul, Republic of Korea.

12. Department of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, USA.

13. Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA.

14. Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Abstract

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. Li et 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

Funder

National Science Foundation

National Institutes of Health

Claudia Adams Barr Program in Cancer Research

Claudia Adams Barr

Dana-Farber Cancer Institute

Rosztoczy Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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