Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs

Immunoglobulins are highly diverse protein sequences that are processed and presented to T-cells by B-cells and other antigen presenting cells. We examined a large dataset of immunoglobulin heavy chain variable regions (IGHV) to assess the diversity of T-cell exposed motifs (TCEM). TCEM comprise tho...

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Main Authors: Robert D. Bremel, E. Jane Homan
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-10-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00541/full
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author Robert D. Bremel
E. Jane Homan
author_facet Robert D. Bremel
E. Jane Homan
author_sort Robert D. Bremel
collection DOAJ
description Immunoglobulins are highly diverse protein sequences that are processed and presented to T-cells by B-cells and other antigen presenting cells. We examined a large dataset of immunoglobulin heavy chain variable regions (IGHV) to assess the diversity of T-cell exposed motifs (TCEM). TCEM comprise those amino acids in a MHC-bound peptide which face outwards, surrounded by the MHC histotope, and which engage the T-cell receptor. Within IGHV there is a distinct pattern of predicted MHC class II binding and a very high frequency of re-use of the TCEMs. The re-use frequency indicates that only a limited number of different cognate T-cells are required to engage many different clonal B-cells. The amino acids in each outward-facing TCEM are intercalated with the amino acids of inward-facing MHC groove-exposed motifs (GEM). Different GEM may have differing, allele-specific, MHC binding affinities. The intercalation of TCEM and GEM in a peptide allows for a vast combinatorial repertoire of epitopes, each eliciting a different response. Outcome of T-cell receptor binding is determined by overall signal strength, which is a function of the number of responding T-cells and the duration of engagement. Hence, the frequency of T-cell exposed motif re-use appears to be an important determinant of whether a T-cell response is stimulatory or suppressive. The frequency distribution of TCEMs implies that somatic hypermutation is followed by clonal expansion that develop along repeated pathways. The observations of TCEM and GEM derived from immunoglobulins suggest a relatively simple, yet powerful, mechanism to correlate T-cell polyspecificity, through re-use of TCEMs, with a very high degree of specificity achieved by combination with a diversity of GEMs. The frequency profile of TCEMs also points to an economical mechanism for maintaining T-cell memory, recall, and self-discrimination based on an endogenously generated profile of motifs.
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spelling doaj.art-0a43a3509c814a648893192a3a9c48892022-12-21T17:15:53ZengFrontiers Media S.A.Frontiers in Immunology1664-32242014-10-01510.3389/fimmu.2014.00541115982Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCsRobert D. Bremel0E. Jane Homan1EigenBio LLCEigenBio LLCImmunoglobulins are highly diverse protein sequences that are processed and presented to T-cells by B-cells and other antigen presenting cells. We examined a large dataset of immunoglobulin heavy chain variable regions (IGHV) to assess the diversity of T-cell exposed motifs (TCEM). TCEM comprise those amino acids in a MHC-bound peptide which face outwards, surrounded by the MHC histotope, and which engage the T-cell receptor. Within IGHV there is a distinct pattern of predicted MHC class II binding and a very high frequency of re-use of the TCEMs. The re-use frequency indicates that only a limited number of different cognate T-cells are required to engage many different clonal B-cells. The amino acids in each outward-facing TCEM are intercalated with the amino acids of inward-facing MHC groove-exposed motifs (GEM). Different GEM may have differing, allele-specific, MHC binding affinities. The intercalation of TCEM and GEM in a peptide allows for a vast combinatorial repertoire of epitopes, each eliciting a different response. Outcome of T-cell receptor binding is determined by overall signal strength, which is a function of the number of responding T-cells and the duration of engagement. Hence, the frequency of T-cell exposed motif re-use appears to be an important determinant of whether a T-cell response is stimulatory or suppressive. The frequency distribution of TCEMs implies that somatic hypermutation is followed by clonal expansion that develop along repeated pathways. The observations of TCEM and GEM derived from immunoglobulins suggest a relatively simple, yet powerful, mechanism to correlate T-cell polyspecificity, through re-use of TCEMs, with a very high degree of specificity achieved by combination with a diversity of GEMs. The frequency profile of TCEMs also points to an economical mechanism for maintaining T-cell memory, recall, and self-discrimination based on an endogenously generated profile of motifs.http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00541/fullMemorybioinformaticsRegulatory T CellT-cell biologyB-cell T cell cooperationPolyspecificity
spellingShingle Robert D. Bremel
E. Jane Homan
Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs
Frontiers in Immunology
Memory
bioinformatics
Regulatory T Cell
T-cell biology
B-cell T cell cooperation
Polyspecificity
title Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs
title_full Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs
title_fullStr Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs
title_full_unstemmed Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs
title_short Frequency patterns of T-cell exposed motifs in immunoglobulin heavy chain peptides presented by MHCs
title_sort frequency patterns of t cell exposed motifs in immunoglobulin heavy chain peptides presented by mhcs
topic Memory
bioinformatics
Regulatory T Cell
T-cell biology
B-cell T cell cooperation
Polyspecificity
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00541/full
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