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How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism

T cell signaling begins with the ligation of the T cell antigen receptor (TCR) by a cognate peptide and the phosphorylation of the receptor’s immunoreceptor tyrosine-based activation motif domains by the kinase Lck. However, the canonical receptor model is insufficient to explain how the constitutiv...

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Detalles Bibliográficos
Autores principales: Rossy, Jérémie, Williamson, David J., Gaus, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377954/
https://www.ncbi.nlm.nih.gov/pubmed/22723799
http://dx.doi.org/10.3389/fimmu.2012.00167
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author Rossy, Jérémie
Williamson, David J.
Gaus, Katharina
author_facet Rossy, Jérémie
Williamson, David J.
Gaus, Katharina
author_sort Rossy, Jérémie
collection PubMed
description T cell signaling begins with the ligation of the T cell antigen receptor (TCR) by a cognate peptide and the phosphorylation of the receptor’s immunoreceptor tyrosine-based activation motif domains by the kinase Lck. However, the canonical receptor model is insufficient to explain how the constitutively active kinase Lck can discriminate between non-ligated and ligated TCRs. Here, we discuss the factors that are thought to regulate the spatial distribution of the TCR and Lck, and therefore critically influence TCR signaling initiation.
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spelling pubmed-33779542012-06-21 How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism Rossy, Jérémie Williamson, David J. Gaus, Katharina Front Immunol Immunology T cell signaling begins with the ligation of the T cell antigen receptor (TCR) by a cognate peptide and the phosphorylation of the receptor’s immunoreceptor tyrosine-based activation motif domains by the kinase Lck. However, the canonical receptor model is insufficient to explain how the constitutively active kinase Lck can discriminate between non-ligated and ligated TCRs. Here, we discuss the factors that are thought to regulate the spatial distribution of the TCR and Lck, and therefore critically influence TCR signaling initiation. Frontiers Research Foundation 2012-06-19 /pmc/articles/PMC3377954/ /pubmed/22723799 http://dx.doi.org/10.3389/fimmu.2012.00167 Text en Copyright © Rossy, Williamson and Gaus. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) , which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Immunology
Rossy, Jérémie
Williamson, David J.
Gaus, Katharina
How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism
title How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism
title_full How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism
title_fullStr How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism
title_full_unstemmed How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism
title_short How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism
title_sort how does the kinase lck phosphorylate the t cell receptor? spatial organization as a regulatory mechanism
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377954/
https://www.ncbi.nlm.nih.gov/pubmed/22723799
http://dx.doi.org/10.3389/fimmu.2012.00167
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