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Article: Mining of linear B cell epitopes of SARS-CoV-2 ORF8 protein from COVID-19 patients

TitleMining of linear B cell epitopes of SARS-CoV-2 ORF8 protein from COVID-19 patients
Authors
KeywordsSARS-CoV-2
ORF8
COVID-19
peptide
epitope
Issue Date2021
PublisherTaylor & Francis, published in association with Shanghai Shangyixun Cultural Communication Company. The Journal's web site is located at https://www.tandfonline.com/toc/temi20/current
Citation
Emerging Microbes & Infections, 2021, v. 10, p. 1016-1023 How to Cite?
AbstractGiven the on-going SARS-CoV-2 pandemic, identification of immunogenic targets against the viral protein will provide crucial advances towards the development of sensitive diagnostic tools and vaccination strategies. Our previous study has found that ORF8 protein of SARS-CoV-2 is highly immunogenic and shows high sensitivity in identifying COVID-19 disease. In this study, by employing overlapping linear peptides, we characterized the IgG immunodominant regions on SARS-CoV-2 ORF8 protein that are seropositive in the sera from SARS-CoV-2-infected patients. The major immunogenic epitopes are localized at (1) N-termini alpha helix, (2) the resides spanning beta 2 and 3 sheets, and (3) the loop between beta 4 and 5 sheets. Additionally, hamster model infected by SARS-CoV-2 further validates the seropositivity of the linear epitopes in vivo, demonstrating a potential application of the linear peptide-based immunization strategy. Taken together, identification and validation of these B-cell linear epitopes will provide insights into the design of serological diagnostics and peptide-based vaccination approach against this pandemic virus of high priority.
Persistent Identifierhttp://hdl.handle.net/10722/303986
ISSN
2021 Impact Factor: 19.568
2020 SCImago Journal Rankings: 2.475
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, X-
dc.contributor.authorLam, JY-
dc.contributor.authorChen, L-
dc.contributor.authorAu, SWN-
dc.contributor.authorTo, KKW-
dc.contributor.authorYuen, KY-
dc.contributor.authorKok, KH-
dc.date.accessioned2021-09-23T08:53:37Z-
dc.date.available2021-09-23T08:53:37Z-
dc.date.issued2021-
dc.identifier.citationEmerging Microbes & Infections, 2021, v. 10, p. 1016-1023-
dc.identifier.issn2222-1751-
dc.identifier.urihttp://hdl.handle.net/10722/303986-
dc.description.abstractGiven the on-going SARS-CoV-2 pandemic, identification of immunogenic targets against the viral protein will provide crucial advances towards the development of sensitive diagnostic tools and vaccination strategies. Our previous study has found that ORF8 protein of SARS-CoV-2 is highly immunogenic and shows high sensitivity in identifying COVID-19 disease. In this study, by employing overlapping linear peptides, we characterized the IgG immunodominant regions on SARS-CoV-2 ORF8 protein that are seropositive in the sera from SARS-CoV-2-infected patients. The major immunogenic epitopes are localized at (1) N-termini alpha helix, (2) the resides spanning beta 2 and 3 sheets, and (3) the loop between beta 4 and 5 sheets. Additionally, hamster model infected by SARS-CoV-2 further validates the seropositivity of the linear epitopes in vivo, demonstrating a potential application of the linear peptide-based immunization strategy. Taken together, identification and validation of these B-cell linear epitopes will provide insights into the design of serological diagnostics and peptide-based vaccination approach against this pandemic virus of high priority.-
dc.languageeng-
dc.publisherTaylor & Francis, published in association with Shanghai Shangyixun Cultural Communication Company. The Journal's web site is located at https://www.tandfonline.com/toc/temi20/current-
dc.relation.ispartofEmerging Microbes & Infections-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectSARS-CoV-2-
dc.subjectORF8-
dc.subjectCOVID-19-
dc.subjectpeptide-
dc.subjectepitope-
dc.titleMining of linear B cell epitopes of SARS-CoV-2 ORF8 protein from COVID-19 patients-
dc.typeArticle-
dc.identifier.emailWang, X: xiaohuiwang@hku.hk-
dc.identifier.emailTo, KKW: kelvinto@hku.hk-
dc.identifier.emailYuen, KY: kyyuen@hkucc.hku.hk-
dc.identifier.emailKok, KH: khkok@hku.hk-
dc.identifier.authorityWang, X=rp02664-
dc.identifier.authorityTo, KKW=rp01384-
dc.identifier.authorityYuen, KY=rp00366-
dc.identifier.authorityKok, KH=rp01455-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1080/22221751.2021.1931465-
dc.identifier.pmid34003073-
dc.identifier.pmcidPMC8186430-
dc.identifier.scopuseid_2-s2.0-85107213409-
dc.identifier.hkuros325584-
dc.identifier.volume10-
dc.identifier.spage1016-
dc.identifier.epage1023-
dc.identifier.isiWOS:000657505200001-
dc.publisher.placeUnited Kingdom-

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