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.
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Authors | Hongbo Hu, 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 |
Journal | Journal of combinatorial chemistry
(J Comb Chem)
2005 Sep-Oct
Vol. 7
Issue 5
Pg. 648-56
ISSN: 1520-4766 [Print] United States |
PMID | 16153058
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antigens, Viral
- Epitopes, B-Lymphocyte
- Peptide Library
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Topics |
- Amino Acid Sequence
- Antigens, Viral
(chemistry, genetics, immunology)
- Combinatorial Chemistry Techniques
- Epitopes, B-Lymphocyte
(chemistry, genetics, immunology)
- Molecular Sequence Data
- Peptide Library
- Severe acute respiratory syndrome-related coronavirus
(chemistry, immunology)
- Severe Acute Respiratory Syndrome
(immunology)
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