dc.rights.license | CC-BY-NC-ND | |
dc.contributor.advisor | Vries, Robert de | |
dc.contributor.author | Linthorst, Mirte | |
dc.date.accessioned | 2023-12-31T00:00:51Z | |
dc.date.available | 2023-12-31T00:00:51Z | |
dc.date.issued | 2023 | |
dc.identifier.uri | https://studenttheses.uu.nl/handle/20.500.12932/45679 | |
dc.description.abstract | SARS-CoV-2 virus is one of the seven known human coronaviruses. At the end of 2019, this virus emerged in China and caused a worldwide pandemic. Since the beginning of the current coronavirus pandemic, the initial spike protein of SARS-CoV-2 has undergone several adaptive mutations in its gene, leading to new variants, coined as variants of concern (VOC). In this study, the receptor binding properties of the N-terminal (NTD) and C-terminal domain (CTD) of P.1, B.1.1.7, B.1.351 and B.1.351 R246I VOCs to cultured VERO-E6 cells and paraffin-embedded lung tissues of several animal models were investigated and compared to wildtype SARS-CoV-2. The obtained data provides grounds for increased binding properties of P.1-CTD and B.1.1.7-CTD, a newly introduced binding site in B.1.351-NTD as well as for B.1.351 R246I-NTD and a host range extension to mice for all four variants. | |
dc.description.sponsorship | Utrecht University | |
dc.language.iso | EN | |
dc.subject | In this study, monomeric and trimeric NTDs and CTDs of HCoVs and VOCs were cloned and expressed to be of use in a range of biological assays. Binding properties of the NTD and CTD of VOC P.1, B.1.1.7, B.1.351 and B.1.351 R246I to cultured VERO-E6 cells and paraffin embedded lung tissues of several animal models were investigated and compared to wt SARS-CoV-2. | |
dc.title | Expression and Binding of SARS-CoV-2 Variant of Concern Spike Proteins | |
dc.type.content | Master Thesis | |
dc.rights.accessrights | Open Access | |
dc.subject.keywords | SARS-CoV-2;Variant of Concern;human coronavirus;C-terminal domain;N-terminal domain;binding properties;VERO-E6;lung tissues | |
dc.subject.courseuu | Molecular and Cellular Life Sciences | |
dc.thesis.id | 2849 | |