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dc.contributor.authorRochman, Nash D
dc.contributor.authorFaure, Guilhem
dc.contributor.authorWolf, Yuri I
dc.contributor.authorFreddolino, Peter L
dc.contributor.authorZhang, Feng
dc.contributor.authorKoonin, Eugene V
dc.date.accessioned2023-04-04T17:19:38Z
dc.date.available2023-04-04T17:19:38Z
dc.date.issued2022-04-26
dc.identifier.urihttps://hdl.handle.net/1721.1/150406
dc.description.abstract<jats:p>Emergence of vaccine escape variants of SARS-CoV-2 is arguably the most pressing problem during the COVID-19 pandemic as vaccines are distributed worldwide. We employed a computational approach to assess the risk of antibody escape resulting from mutations in the receptor-binding domain of the spike protein of the wild-type SARS-CoV-2 virus as well as the Delta, Gamma, and Omicron variants.</jats:p>en_US
dc.language.isoen
dc.publisherAmerican Society for Microbiologyen_US
dc.relation.isversionof10.1128/mbio.00135-22en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceASMen_US
dc.titleEpistasis at the SARS-CoV-2 Receptor-Binding Domain Interface and the Propitiously Boring Implications for Vaccine Escapeen_US
dc.typeArticleen_US
dc.identifier.citationRochman, Nash D, Faure, Guilhem, Wolf, Yuri I, Freddolino, Peter L, Zhang, Feng et al. 2022. "Epistasis at the SARS-CoV-2 Receptor-Binding Domain Interface and the Propitiously Boring Implications for Vaccine Escape." mBio, 13 (2).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.relation.journalmBioen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-04-04T17:17:02Z
dspace.orderedauthorsRochman, ND; Faure, G; Wolf, YI; Freddolino, PL; Zhang, F; Koonin, EVen_US
dspace.date.submission2023-04-04T17:17:05Z
mit.journal.volume13en_US
mit.journal.issue2en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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