Synthetic peptides outside the spike protein heptad repeat regions as potent inhibitors of SARS-associated coronavirus - PubMed (original) (raw)
Yi Guan, Ming-Liang Hez, Hongzhe Sun, Lanying Du, Ying Zheng, Kin-Ling Wong, Honglin Chen, Ying Chen, Linyu Lu, Julian A Tanner, Rory M Watt, Neri Niccolai, Andrea Bernini, Ottavia Spiga, Patrick C Y Woo, Hsiang-fu Kung, Kwok-Yung Yuen, Jian-Dong Huang
Affiliations
- PMID: 15918330
Synthetic peptides outside the spike protein heptad repeat regions as potent inhibitors of SARS-associated coronavirus
Bo-Jion Zheng et al. Antivir Ther. 2005.
Abstract
A novel severe acute respiratory syndrome (SARS)-associated coronavirus (SARS-CoV) has been identified as the aetiological agent of SARS. We previously isolated and characterized SARS-CoV and SARS-CoV-like viruses from human and animals, respectively, suggesting that SARS could be transmitted from wild/farmed animals to humans. Comparison of the viral genomes indicated that sequence variation between animal and human isolates existed mainly in the spike (S) gene. We hypothesized that these variations may underlie a change of binding specificity of the S protein to the host cells, permitting viral transmission from animals to humans. Here we report that four 20-mer synthetic peptides (S protein fragments), designed to span these sequence variation hotspots, exhibited significant antiviral activities in a cell line. SARS-CoV infectivity was reduced over 10 000-fold through pre-incubation with two of these peptides, while it was completely inhibited in the presence of three peptides. Molecular modelling of the SARS-CoV peplomer suggests that three of these antiviral peptides map to the interfaces between the three monomers of the trimeric peplomer rather than the heptad repeat region from which short peptides are known to inhibit viral entry. Our results revealed novel regions in the spike protein that can be targeted to inhibit viral infection. The peptides identified in this study could be further developed into antiviral drugs.
Similar articles
- Inhibition of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) infectivity by peptides analogous to the viral spike protein.
Sainz B Jr, Mossel EC, Gallaher WR, Wimley WC, Peters CJ, Wilson RB, Garry RF. Sainz B Jr, et al. Virus Res. 2006 Sep;120(1-2):146-55. doi: 10.1016/j.virusres.2006.03.001. Epub 2006 Apr 17. Virus Res. 2006. PMID: 16616792 Free PMC article. - Interaction between heptad repeat 1 and 2 regions in spike protein of SARS-associated coronavirus: implications for virus fusogenic mechanism and identification of fusion inhibitors.
Liu S, Xiao G, Chen Y, He Y, Niu J, Escalante CR, Xiong H, Farmar J, Debnath AK, Tien P, Jiang S. Liu S, et al. Lancet. 2004 Mar 20;363(9413):938-47. doi: 10.1016/S0140-6736(04)15788-7. Lancet. 2004. PMID: 15043961 Free PMC article. - Template-based coiled-coil antigens elicit neutralizing antibodies to the SARS-coronavirus.
Tripet B, Kao DJ, Jeffers SA, Holmes KV, Hodges RS. Tripet B, et al. J Struct Biol. 2006 Aug;155(2):176-94. doi: 10.1016/j.jsb.2006.03.019. Epub 2006 Apr 27. J Struct Biol. 2006. PMID: 16697221 Free PMC article. - Severe acute respiratory syndrome coronavirus entry as a target of antiviral therapies.
Kuhn JH, Li W, Radoshitzky SR, Choe H, Farzan M. Kuhn JH, et al. Antivir Ther. 2007;12(4 Pt B):639-50. Antivir Ther. 2007. PMID: 17944271 Review. - An overall picture of SARS coronavirus (SARS-CoV) genome-encoded major proteins: structures, functions and drug development.
Chen S, Luo H, Chen L, Chen J, Shen J, Zhu W, Chen K, Shen X, Jiang H. Chen S, et al. Curr Pharm Des. 2006;12(35):4539-53. doi: 10.2174/138161206779010459. Curr Pharm Des. 2006. PMID: 17168760 Review.
Cited by
- Broad-spectrum antivirals for the emerging Middle East respiratory syndrome coronavirus.
Chan JF, Chan KH, Kao RY, To KK, Zheng BJ, Li CP, Li PT, Dai J, Mok FK, Chen H, Hayden FG, Yuen KY. Chan JF, et al. J Infect. 2013 Dec;67(6):606-16. doi: 10.1016/j.jinf.2013.09.029. Epub 2013 Oct 3. J Infect. 2013. PMID: 24096239 Free PMC article. - The bright and dark sides of protein conformational switches and the unifying forces of infections.
Sannigrahi A, De N, Chattopadhyay K. Sannigrahi A, et al. Commun Biol. 2020 Jul 15;3(1):382. doi: 10.1038/s42003-020-1115-x. Commun Biol. 2020. PMID: 32669705 Free PMC article. Review. - Adaptive evolution of the spike gene of SARS coronavirus: changes in positively selected sites in different epidemic groups.
Zhang CY, Wei JF, He SH. Zhang CY, et al. BMC Microbiol. 2006 Oct 4;6:88. doi: 10.1186/1471-2180-6-88. BMC Microbiol. 2006. PMID: 17020602 Free PMC article. - Coronaviruses - drug discovery and therapeutic options.
Zumla A, Chan JF, Azhar EI, Hui DS, Yuen KY. Zumla A, et al. Nat Rev Drug Discov. 2016 May;15(5):327-47. doi: 10.1038/nrd.2015.37. Epub 2016 Feb 12. Nat Rev Drug Discov. 2016. PMID: 26868298 Free PMC article. Review. - Severe acute respiratory syndrome coronavirus as an agent of emerging and reemerging infection.
Cheng VC, Lau SK, Woo PC, Yuen KY. Cheng VC, et al. Clin Microbiol Rev. 2007 Oct;20(4):660-94. doi: 10.1128/CMR.00023-07. Clin Microbiol Rev. 2007. PMID: 17934078 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Miscellaneous