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Synthetic peptides derived from SARS coronavirus S protein with diagnostic and therapeutic potential

  • Wei Lu
  • , 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 Sun
*此作品的通讯作者
  • CAS - Shanghai Institute of Nutrition and Health
  • Academy of Military Medical Science China
  • Bioinformation Center
  • Immunology Division

科研成果: 期刊稿件文章同行评审

摘要

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.

源语言英语
页(从-至)2130-2136
页数7
期刊FEBS Letters
579
10
DOI
出版状态已出版 - 11 4月 2005
已对外发布

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