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Screening and identification of linear B-cell epitopes and entry-blocking peptide of severe acute respiratory syndrome (SARS)-associated coronavirus using synthetic overlapping peptide library.

Identifieur interne : 006703 ( Main/Exploration ); précédent : 006702; suivant : 006704

Screening and identification of linear B-cell epitopes and entry-blocking peptide of severe acute respiratory syndrome (SARS)-associated coronavirus using synthetic overlapping peptide library.

Auteurs : Hongbo Hu [République populaire de Chine] ; Li Li ; Richard Y. Kao ; Binbin Kou ; Zhanguo Wang ; Liang Zhang ; Huiyuan Zhang ; Zhiyong Hao ; Wayne H. Tsui ; Anping Ni ; Lianxian Cui ; Baoxing Fan ; Feng Guo ; Shuan Rao ; Chengyu Jiang ; Qian Li ; Manji Sun ; Wei He ; Gang Liu

Source :

RBID : pubmed:16153058

Descripteurs français

English descriptors

Abstract

A 10-mer overlapping peptide library has been synthesized for screening and identification of linear B-cell epitopes of severe acute respiratory syndrome associated coronavirus (SARS-CoV), which spanned the major structural proteins of SARS-CoV. One hundred and eleven candidate peptides were positive according to the result of PEPscan, which were assembled into 22 longer peptides. Five of these peptides showed high cross-immunoreactivities (approximately 66.7 to 90.5%) to SARS convalescent patients' sera from the severest epidemic regions of the China mainland. Most interestingly, S(471-503), a peptide located at the receptor binding domain (RBD) of SARS-CoV, could specifically block the binding between the RBD and angiotensin-converting enzyme 2, resulting in the inhibition of SARS-CoV entrance into host cells in vitro. The study demonstrated that S(471-503) peptide was a potential immunoantigen for the development of peptide-based vaccine or a candidate for further drug evaluation against the SARS-CoV virus-cell fusion.

DOI: 10.1021/cc0500607
PubMed: 16153058


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Li, Qian" sort="Li, Qian" uniqKey="Li Q" first="Qian" last="Li">Qian Li</name>
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<name sortKey="Sun, Manji" sort="Sun, Manji" uniqKey="Sun M" first="Manji" last="Sun">Manji Sun</name>
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<term>Amino Acid Sequence</term>
<term>Antigens, Viral (chemistry)</term>
<term>Antigens, Viral (genetics)</term>
<term>Antigens, Viral (immunology)</term>
<term>Combinatorial Chemistry Techniques</term>
<term>Epitopes, B-Lymphocyte (chemistry)</term>
<term>Epitopes, B-Lymphocyte (genetics)</term>
<term>Epitopes, B-Lymphocyte (immunology)</term>
<term>Molecular Sequence Data</term>
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<term>Antigènes viraux (immunologie)</term>
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<term>Données de séquences moléculaires</term>
<term>Déterminants antigéniques des lymphocytes B ()</term>
<term>Déterminants antigéniques des lymphocytes B (génétique)</term>
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<term>Antigens, Viral</term>
<term>Epitopes, B-Lymphocyte</term>
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<term>Antigens, Viral</term>
<term>Epitopes, B-Lymphocyte</term>
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<term>Banque de peptides</term>
<term>Données de séquences moléculaires</term>
<term>Déterminants antigéniques des lymphocytes B</term>
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<front>
<div type="abstract" xml:lang="en">A 10-mer overlapping peptide library has been synthesized for screening and identification of linear B-cell epitopes of severe acute respiratory syndrome associated coronavirus (SARS-CoV), which spanned the major structural proteins of SARS-CoV. One hundred and eleven candidate peptides were positive according to the result of PEPscan, which were assembled into 22 longer peptides. Five of these peptides showed high cross-immunoreactivities (approximately 66.7 to 90.5%) to SARS convalescent patients' sera from the severest epidemic regions of the China mainland. Most interestingly, S(471-503), a peptide located at the receptor binding domain (RBD) of SARS-CoV, could specifically block the binding between the RBD and angiotensin-converting enzyme 2, resulting in the inhibition of SARS-CoV entrance into host cells in vitro. The study demonstrated that S(471-503) peptide was a potential immunoantigen for the development of peptide-based vaccine or a candidate for further drug evaluation against the SARS-CoV virus-cell fusion.</div>
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