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Epitope mapping and evaluation of specificity of T-helper sites in four major antigenic peptides of chicken riboflavin carrier protein in outbred rats.

Identifieur interne : 003221 ( Main/Exploration ); précédent : 003220; suivant : 003222

Epitope mapping and evaluation of specificity of T-helper sites in four major antigenic peptides of chicken riboflavin carrier protein in outbred rats.

Auteurs : Sarada Subramanian [Inde] ; S. Andal ; Anjali A. Karande ; P. Radhakantha Adiga

Source :

RBID : pubmed:14575688

Descripteurs français

English descriptors

Abstract

This paper reviews our studies on synthetic peptides spanning the major antigenic determinants of the chicken riboflavin carrier protein (RCP; 219 AA). These determinants are composed of residues 4-24 (YGC), 64-83 (CED), 130-147 (GEN), and 200-219 (HAC) and function as minivaccines in terms of eliciting anti-peptide antibodies which recognize the native protein and are particularly promising contraceptive vaccine candidates. We have used 15-residue synthetic peptides to define short sequences involved in interaction with antibody and with T-cells. We have mapped the boundaries of T-cell epitopes of these peptides in outbred rats by immunizing the animals with each peptide and assaying the popliteal lymph node cell proliferation against a series of overlapping synthetic 15-mers covering the entire length of the individual peptides. The peptides YGC, GEN, and HAC harboured a single T-cell epitope each whereas the peptide CED exhibited bimodal response possessing two epitopes, one at N-terminus and the other at the C-terminus. These studies provide insight into the way in which an immunogen is viewed by the immune system. In addition, preferential T-cell helper function for B cells recognizing unique determinants on the same molecule was demonstrated. This information helps in exploiting synthetic peptides in the construction of designer immunogens which have potential as candidate vaccines.

DOI: 10.1016/j.bbrc.2003.09.162
PubMed: 14575688


Affiliations:


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<term>Carrier Proteins (immunology)</term>
<term>Cells, Cultured</term>
<term>Chickens</term>
<term>Epitope Mapping (methods)</term>
<term>Epitopes (chemistry)</term>
<term>Epitopes, T-Lymphocyte (chemistry)</term>
<term>Epitopes, T-Lymphocyte (immunology)</term>
<term>Membrane Transport Proteins</term>
<term>Molecular Sequence Data</term>
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<term>Peptides (classification)</term>
<term>Peptides (immunology)</term>
<term>Rats</term>
<term>Rats, Wistar</term>
<term>Sensitivity and Specificity</term>
<term>Sequence Analysis, Protein (methods)</term>
<term>T-Lymphocytes, Helper-Inducer (chemistry)</term>
<term>T-Lymphocytes, Helper-Inducer (immunology)</term>
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<term>Vaccines, Contraceptive (immunology)</term>
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<term>Analyse de séquence de protéine ()</term>
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<term>Cellules cultivées</term>
<term>Données de séquences moléculaires</term>
<term>Déterminants antigéniques des lymphocytes T ()</term>
<term>Déterminants antigéniques des lymphocytes T (immunologie)</term>
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<term>Lymphocytes T auxiliaires (immunologie)</term>
<term>Peptides ()</term>
<term>Peptides (immunologie)</term>
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<term>Protéines de transport ()</term>
<term>Protéines de transport (immunologie)</term>
<term>Protéines de transport membranaire</term>
<term>Rat Wistar</term>
<term>Rats</term>
<term>Sensibilité et spécificité</term>
<term>Séquence d'acides aminés</term>
<term>Vaccins contraceptifs ()</term>
<term>Vaccins contraceptifs (immunologie)</term>
<term>Épitopes ()</term>
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<term>Données de séquences moléculaires</term>
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<div type="abstract" xml:lang="en">This paper reviews our studies on synthetic peptides spanning the major antigenic determinants of the chicken riboflavin carrier protein (RCP; 219 AA). These determinants are composed of residues 4-24 (YGC), 64-83 (CED), 130-147 (GEN), and 200-219 (HAC) and function as minivaccines in terms of eliciting anti-peptide antibodies which recognize the native protein and are particularly promising contraceptive vaccine candidates. We have used 15-residue synthetic peptides to define short sequences involved in interaction with antibody and with T-cells. We have mapped the boundaries of T-cell epitopes of these peptides in outbred rats by immunizing the animals with each peptide and assaying the popliteal lymph node cell proliferation against a series of overlapping synthetic 15-mers covering the entire length of the individual peptides. The peptides YGC, GEN, and HAC harboured a single T-cell epitope each whereas the peptide CED exhibited bimodal response possessing two epitopes, one at N-terminus and the other at the C-terminus. These studies provide insight into the way in which an immunogen is viewed by the immune system. In addition, preferential T-cell helper function for B cells recognizing unique determinants on the same molecule was demonstrated. This information helps in exploiting synthetic peptides in the construction of designer immunogens which have potential as candidate vaccines.</div>
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