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Components of the Ligand for a Ni(++) Reactive Human T Cell Clone

The major histocompatibility complex (MHC) restriction element for a human Ni(2+) reactive T cell, ANi-2.3, was identified as DR52c. A series of experiments established that the functional ligand for this T cell was a preformed complex of Ni(2+) bound to the combination of DR52c and a specific pepti...

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Autores principales: Lu, Linh, Vollmer, Jörg, Moulon, Corinne, Weltzien, Hans Ulrich, Marrack, Philippa, Kappler, John
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193829/
https://www.ncbi.nlm.nih.gov/pubmed/12615898
http://dx.doi.org/10.1084/jem.20021762
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author Lu, Linh
Vollmer, Jörg
Moulon, Corinne
Weltzien, Hans Ulrich
Marrack, Philippa
Kappler, John
author_facet Lu, Linh
Vollmer, Jörg
Moulon, Corinne
Weltzien, Hans Ulrich
Marrack, Philippa
Kappler, John
author_sort Lu, Linh
collection PubMed
description The major histocompatibility complex (MHC) restriction element for a human Ni(2+) reactive T cell, ANi-2.3, was identified as DR52c. A series of experiments established that the functional ligand for this T cell was a preformed complex of Ni(2+) bound to the combination of DR52c and a specific peptide that was generated in human and mouse B cells, but not in fibroblasts nor other antigen processing–deficient cells. In addition, ANi-2.3 recognition of this complex was dependent on His81 of the MHC β chain, suggesting a role for this amino acid in Ni(2+) binding to MHC. We propose a general model for Ni(2+) recognition in which βHis81 and two amino acids from the NH(2)-terminal part of the MHC bound peptide coordinate Ni(2+) which then interacts with some portion of the Vα CDR1 or CDR2 region.
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spelling pubmed-21938292008-04-11 Components of the Ligand for a Ni(++) Reactive Human T Cell Clone Lu, Linh Vollmer, Jörg Moulon, Corinne Weltzien, Hans Ulrich Marrack, Philippa Kappler, John J Exp Med Article The major histocompatibility complex (MHC) restriction element for a human Ni(2+) reactive T cell, ANi-2.3, was identified as DR52c. A series of experiments established that the functional ligand for this T cell was a preformed complex of Ni(2+) bound to the combination of DR52c and a specific peptide that was generated in human and mouse B cells, but not in fibroblasts nor other antigen processing–deficient cells. In addition, ANi-2.3 recognition of this complex was dependent on His81 of the MHC β chain, suggesting a role for this amino acid in Ni(2+) binding to MHC. We propose a general model for Ni(2+) recognition in which βHis81 and two amino acids from the NH(2)-terminal part of the MHC bound peptide coordinate Ni(2+) which then interacts with some portion of the Vα CDR1 or CDR2 region. The Rockefeller University Press 2003-03-03 /pmc/articles/PMC2193829/ /pubmed/12615898 http://dx.doi.org/10.1084/jem.20021762 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Lu, Linh
Vollmer, Jörg
Moulon, Corinne
Weltzien, Hans Ulrich
Marrack, Philippa
Kappler, John
Components of the Ligand for a Ni(++) Reactive Human T Cell Clone
title Components of the Ligand for a Ni(++) Reactive Human T Cell Clone
title_full Components of the Ligand for a Ni(++) Reactive Human T Cell Clone
title_fullStr Components of the Ligand for a Ni(++) Reactive Human T Cell Clone
title_full_unstemmed Components of the Ligand for a Ni(++) Reactive Human T Cell Clone
title_short Components of the Ligand for a Ni(++) Reactive Human T Cell Clone
title_sort components of the ligand for a ni(++) reactive human t cell clone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193829/
https://www.ncbi.nlm.nih.gov/pubmed/12615898
http://dx.doi.org/10.1084/jem.20021762
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