Slow phosphorylation of a tyrosine residue in LAT optimizes T cell ligand discrimination-Reference-Cited by-同舟云学术

Slow phosphorylation of a tyrosine residue in LAT optimizes T cell ligand discrimination

Published:2019-10-14 Issue:11 Volume:20 Page:1481-1493
ISSN:1529-2908
Container-title:Nature Immunology
language:en
Short-container-title:Nat Immunol

Author:

Lo Wan-Lin,Shah Neel H.^ORCID,Rubin Sara A.^ORCID,Zhang Weiguo,Horkova Veronika^ORCID,Fallahee Ian R.,Stepanek Ondrej^ORCID,Zon Leonard I.,Kuriyan John,Weiss Arthur^ORCID

Funder

U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases

Howard Hughes Medical Institute

Jane Coffin Childs Memorial Fund for Medical Research

Damon Runyon Cancer Research Foundation

Czech Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://www.nature.com/articles/s41590-019-0502-2.pdf

Reference58 articles.

1. Feinerman, O., Germain, R. N. & Altan-Bonnet, G. Quantitative challenges in understanding ligand discrimination by ɑβ T cells. Mol. Immunol. 45, 619–631 (2008).

2. Brameshuber, M. et al. Monomeric TCRs drive T cell antigen recognition. Nat. Immunol. 19, 487–496 (2018).

3. Chakraborty, A. K. & Weiss, A. Insights into the initiation of TCR signaling. Nat. Immunol. 15, 798–807 (2014).

4. Huang, J. et al. A single peptide-major histocompatibility complex ligand triggers digital cytokine secretion in CD4+ T cells. Immunity 39, 846–857 (2013).

5. Cui, W. & Mehta, P. Identifying feasible operating regimes for early T-cell recognition: the speed, energy, accuracy trade-off in kinetic proofreading and adaptive sorting. PLoS One 13, e0202331 (2018).

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