A highly potent SARS-CoV-2 blocking lectin protein
buir.contributor.author | Ahan, Recep E. | |
buir.contributor.author | Kehribar, Ebru Ş. | |
buir.contributor.author | Özçelik, Cemile E. | |
buir.contributor.author | Bozkurt, Eray U. | |
buir.contributor.author | Şeker, Urartu Özgür Şafak | |
buir.contributor.orcid | Ahan, Recep E.|0000-0002-6061-9062 | |
buir.contributor.orcid | Kehribar, Ebru Ş.|0000-0003-2951-4390 | |
buir.contributor.orcid | Özçelik, Cemile E.|0000-0002-3499-4061 | |
buir.contributor.orcid | Şeker, Urartu Özgür Şafak|0000-0002-5272-1876 | |
dc.citation.epage | 1264 | en_US |
dc.citation.issueNumber | 7 | en_US |
dc.citation.spage | 1253 | en_US |
dc.citation.volumeNumber | 8 | en_US |
dc.contributor.author | Ahan, Recep E. | |
dc.contributor.author | Hanifehnezhad, A. | |
dc.contributor.author | Kehribar, Ebru Ş. | |
dc.contributor.author | Oguzoglu, T. C. | |
dc.contributor.author | Földes, K. | |
dc.contributor.author | Özçelik, Cemile E. | |
dc.contributor.author | Filazi, N. | |
dc.contributor.author | Öztop, S. | |
dc.contributor.author | Palaz, F. | |
dc.contributor.author | Önder, S. | |
dc.contributor.author | Bozkurt, Eray U. | |
dc.contributor.author | Ergünay, K. | |
dc.contributor.author | Özkul, A. | |
dc.contributor.author | Şeker, Urartu Özgür Şafak | |
dc.date.accessioned | 2023-02-14T11:09:07Z | |
dc.date.available | 2023-02-14T11:09:07Z | |
dc.date.issued | 2022-04-15 | |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.description.abstract | The COVID-19 (coronavirus disease-19) pandemic affected more than 180 million people around the globe, causing more than five million deaths as of January 2022. SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2), the new coronavirus, has been identified as the primary cause of the infection. The number of vaccinated people is increasing; however, prophylactic drugs are highly demanded to ensure secure social contact. A number of drug molecules have been repurposed to fight against SARS-CoV-2, and some of them have been proven to be effective in preventing hospitalization or ICU admissions. Here, we demonstrated griffithsin (GRFT), a lectin protein, to block the entry of SARS-CoV-2 and its variants, Delta and Omicron, into the Vero E6 cell lines and IFNAR-/-mouse models by attaching to the spike protein of SARS-CoV-2. Given the current mutation frequency of SARS-CoV-2, we believe that GRFT protein-based drugs will have a high impact in preventing the transmission of both the Wuhan strain as well as any other emerging variants, including Delta and Omicron variants, causing the high-speed spread of COVID-19. | en_US |
dc.identifier.doi | 10.1021/acsinfecdis.2c00006 | en_US |
dc.identifier.eissn | 2373-8227 | |
dc.identifier.issn | 23738227 | |
dc.identifier.uri | http://hdl.handle.net/11693/111255 | |
dc.language.iso | English | en_US |
dc.publisher | American Chemical Society | en_US |
dc.relation.isversionof | https://dx.doi.org/10.1021/acsinfecdis.2c00006 | en_US |
dc.source.title | ACS Infectious Diseases | en_US |
dc.title | A highly potent SARS-CoV-2 blocking lectin protein | en_US |
dc.type | Article | en_US |
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