Selected article for: "acute respiratory syndrome and dipeptidyl peptidase"

Author: Du, Lanying; Zhao, Guangyu; Kou, Zhihua; Ma, Cuiqing; Sun, Shihui; Poon, Vincent K M; Lu, Lu; Wang, Lili; Debnath, Asim K; Zheng, Bo-Jian; Zhou, Yusen; Jiang, Shibo
Title: Identification of a receptor-binding domain in the S protein of the novel human coronavirus Middle East respiratory syndrome coronavirus as an essential target for vaccine development.
  • Cord-id: 4eahae54
  • Document date: 2013_1_1
  • ID: 4eahae54
    Snippet: A novel human Middle East respiratory syndrome coronavirus (MERS-CoV) caused outbreaks of severe acute respiratory syndrome (SARS)-like illness with a high mortality rate, raising concerns of its pandemic potential. Dipeptidyl peptidase-4 (DPP4) was recently identified as its receptor. Here we showed that residues 377 to 662 in the S protein of MERS-CoV specifically bound to DPP4-expressing cells and soluble DPP4 protein and induced significant neutralizing antibody responses, suggesting that th
    Document: A novel human Middle East respiratory syndrome coronavirus (MERS-CoV) caused outbreaks of severe acute respiratory syndrome (SARS)-like illness with a high mortality rate, raising concerns of its pandemic potential. Dipeptidyl peptidase-4 (DPP4) was recently identified as its receptor. Here we showed that residues 377 to 662 in the S protein of MERS-CoV specifically bound to DPP4-expressing cells and soluble DPP4 protein and induced significant neutralizing antibody responses, suggesting that this region contains the receptor-binding domain (RBD), which has a potential to be developed as a MERS-CoV vaccine.

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