Synthetic peptides derived from SARS coronavirus S protein with diagnostic and therapeutic potential.
Identifieur interne : 002807 ( PubMed/Curation ); précédent : 002806; suivant : 002808Synthetic peptides derived from SARS coronavirus S protein with diagnostic and therapeutic potential.
Auteurs : Wei Lu [République populaire de Chine] ; Xiao-Dong Wu ; Mu De Shi ; Rui Fu Yang ; You Yu He ; Chao Bian ; Tie Liu Shi ; Sheng Yang ; Xue-Liang Zhu ; Wei-Hong Jiang ; Yi Xue Li ; Lin-Chen Yan ; Yong Yong Ji ; Ying Lin ; Guo-Mei Lin ; Lin Tian ; Jin Wang ; Hong Xia Wang ; You Hua Xie ; Gang Pei ; Jia Rui Wu ; Bing SunSource :
- FEBS letters [ 0014-5793 ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
- usage thérapeutique : Peptides.
- Biologie informatique, Données de séquences moléculaires, Humains, Peptides, Protéines virales, Séquence d'acides aminés, Technique de Western, Virus du SRAS.
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Peptides, Viral Proteins.
- chemical , therapeutic use : Peptides.
- chemistry : SARS Virus.
- Amino Acid Sequence, Blotting, Western, Computational Biology, Humans, Molecular Sequence Data.
Abstract
The spike (S) protein of severe acute respiratory syndrome coronavirus (SARS-CoV) is an important viral structural protein. Based on bioinformatics analysis, 10 antigenic peptides derived from the S protein sequence were selected and synthesized. The antigenicity and immunoreactivity of all the peptides were tested in vivo and in vitro. Four peptides (P6, P8, P9 and P10) which contain B cell epitopes of the S protein were identified, and P8 peptide was confirmed in vivo to have a potential in serological diagnosis. By using a syncytia formation model, we tested the neutralization ability of all 10 peptides and their corresponding antibodies. It is interesting to find that P8 and P9 peptides inhibited syncytia formation, suggesting that the P8 and P9 spanning regions may provide a good target for anti-SARS-CoV drug design. Our data suggest that we have identified peptides derived from the S protein of SARS-CoV, which are useful for SARS treatment and diagnosis.
DOI: 10.1016/j.febslet.2005.02.070
PubMed: 15811330
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pubmed:15811330Le document en format XML
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<front><div type="abstract" xml:lang="en">The spike (S) protein of severe acute respiratory syndrome coronavirus (SARS-CoV) is an important viral structural protein. Based on bioinformatics analysis, 10 antigenic peptides derived from the S protein sequence were selected and synthesized. The antigenicity and immunoreactivity of all the peptides were tested in vivo and in vitro. Four peptides (P6, P8, P9 and P10) which contain B cell epitopes of the S protein were identified, and P8 peptide was confirmed in vivo to have a potential in serological diagnosis. By using a syncytia formation model, we tested the neutralization ability of all 10 peptides and their corresponding antibodies. It is interesting to find that P8 and P9 peptides inhibited syncytia formation, suggesting that the P8 and P9 spanning regions may provide a good target for anti-SARS-CoV drug design. Our data suggest that we have identified peptides derived from the S protein of SARS-CoV, which are useful for SARS treatment and diagnosis.</div>
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<Abstract><AbstractText>The spike (S) protein of severe acute respiratory syndrome coronavirus (SARS-CoV) is an important viral structural protein. Based on bioinformatics analysis, 10 antigenic peptides derived from the S protein sequence were selected and synthesized. The antigenicity and immunoreactivity of all the peptides were tested in vivo and in vitro. Four peptides (P6, P8, P9 and P10) which contain B cell epitopes of the S protein were identified, and P8 peptide was confirmed in vivo to have a potential in serological diagnosis. By using a syncytia formation model, we tested the neutralization ability of all 10 peptides and their corresponding antibodies. It is interesting to find that P8 and P9 peptides inhibited syncytia formation, suggesting that the P8 and P9 spanning regions may provide a good target for anti-SARS-CoV drug design. Our data suggest that we have identified peptides derived from the S protein of SARS-CoV, which are useful for SARS treatment and diagnosis.</AbstractText>
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