A Molecular Basis for How a Single TCR Interfaces Multiple Ligands

CD8+ T cells respond to Ags when their clonotypic receptor, the TCR, recognizes nonself peptides displayed by MHC class I molecules. The TCR/ligand interactions are degenerate because, in its life time, the TCR interacts with self MHC class I-self peptide complexes during ontogeny and with self clas...

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Veröffentlicht in:The Journal of immunology (1950) 1998-11, Vol.161 (9), p.4719-4727
Hauptverfasser: Boesteanu, Alina, Brehm, Michael, Mylin, Lawrence M, Christianson, Gregory J, Tevethia, Satvir S, Roopenian, Derry C, Joyce, Sebastian
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container_end_page 4727
container_issue 9
container_start_page 4719
container_title The Journal of immunology (1950)
container_volume 161
creator Boesteanu, Alina
Brehm, Michael
Mylin, Lawrence M
Christianson, Gregory J
Tevethia, Satvir S
Roopenian, Derry C
Joyce, Sebastian
description CD8+ T cells respond to Ags when their clonotypic receptor, the TCR, recognizes nonself peptides displayed by MHC class I molecules. The TCR/ligand interactions are degenerate because, in its life time, the TCR interacts with self MHC class I-self peptide complexes during ontogeny and with self class I complexed with nonself peptides to initiate Ag-specific responses. Additionally, the same TCR has the potential to interact with nonself class I complexed with nonself peptides. How a single TCR interfaces multiple ligands remains unclear. Combinatorial synthetic peptide libraries provide a powerful tool to elucidate the rules that dictate how a single TCR engages multiple ligands. Such libraries were used to probe the requirements for TCR recognition by cloned CD8+ T cells directed against Ags presented by H-2Kb class I molecules. When H-2Kb contact residues were examined, position 3 of the peptides proved more critical than the dominant carboxyl-terminal anchor residue. Thus, secondary anchor residues can play a dominant role in determining the antigenicity of the epitope presented by class I molecules. When the four solvent-exposed potential TCR contact residues were examined, only one or two of these positions required structurally similar residues. Considerable structural variability was tolerated at the remaining two or three solvent-exposed residues of the Kb-binding peptides. The TCR, therefore, requires close physico-chemical complementarity with only a few amino acid residues, thus explaining why TCR/MHC interactions are of low affinity and degenerate.
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When the four solvent-exposed potential TCR contact residues were examined, only one or two of these positions required structurally similar residues. Considerable structural variability was tolerated at the remaining two or three solvent-exposed residues of the Kb-binding peptides. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Amino Acid Sequence
Animals
Antigen Presentation
Antigens - chemistry
Antigens - immunology
Antigens - metabolism
Epitopes - chemistry
Epitopes - immunology
Epitopes - metabolism
H-2 Antigens - chemistry
H-2 Antigens - immunology
Ligands
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Models, Immunological
Models, Molecular
Molecular Sequence Data
Peptide Fragments - chemistry
Peptide Fragments - immunology
Peptide Fragments - metabolism
Peptide Library
Protein Binding
Protein Conformation
Receptors, Antigen, T-Cell - chemistry
Receptors, Antigen, T-Cell - metabolism
Structure-Activity Relationship
T-Lymphocytes, Cytotoxic - immunology
title A Molecular Basis for How a Single TCR Interfaces Multiple Ligands
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