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Submit Manuscript Volume 30, No 8, Aug 2020
ISSN: 1001-0602
EISSN: 1748-7838 2018
impact factor 17.848*
(Clarivate Analytics, 2019)
Volume 30 Issue 8, August 2020: 702-704 |
Mining of epitopes on spike protein of SARS-CoV-2 from COVID-19 patients
Bao-zhong Zhang1,2,† , Ye-fan Hu2,3,† , Lin-lei Chen4,† , Thomas Yau3,† , Yi-gang Tong5,† , Jing-chu Hu11 , Jian-piao Cai4 , Kwok-Hung Chan4 , Ying Dou2 , Jian Deng2 , Xiao-lei Wang2 , Ivan Fan-Ngai Hung3 , Kelvin Kai-Wang To4,* , Kwok Yung Yuen4,* , Jian-Dong Huang1,2,*
1CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong 518055, ChinaDear Editor,
The ongoing coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a serious threat to global public health, and is imposing severe burdens on human society. Several candidate vaccines against SARS-CoV-2 are now undergoing clinical trials. The Spike (S) protein of SARS-CoV-2 is widely considered as a promising antigen. However, limited information about the protective immune response against SARS-CoV-2 has been reported.1 In vivo or in natura data of the immune response in patients, including major immune responses to S protein, are currently lacking. The development of effective and safe vaccines against SARS-CoV-2 is urgently needed because of some potential adverse events including antibody-dependent enhancement (ADE),2 which might be difficult to avoid in current vaccine designs. Therefore, it is important to mine serological information from COVID-19 patients. In this study, we analysed the correlation between S- or Nucleocapsid (N) protein-specific antibody levels and neutralizing antibody tires. Furthermore, we aimed to identify linear B cell linear immunodominant (ID) sites on the S protein by Pepscan analysis with a series of overlapped peptides against the sera from COVID-19 patients.
https://doi.org/10.1038/s41422-020-0366-x