7LXZ
SARS-CoV-2 S/S2M11/S2L28 Global Refinement
Summary for 7LXZ
Entry DOI | 10.2210/pdb7lxz/pdb |
EMDB information | 23580 |
Descriptor | Spike glycoprotein, S2M11 Fab Light Chain variable region, S2M11 Fab Heavy Chain variable region, ... (9 entities in total) |
Functional Keywords | antibody, viral protein, structural genomics, seattle structural genomics center for infectious disease, ssgcid, viral protein-immune system complex, viral protein/immune system |
Biological source | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV,SARS-CoV-2) More |
Total number of polymer chains | 15 |
Total formula weight | 593314.80 |
Authors | McCallum, M.,Veesler, D.,Seattle Structural Genomics Center for Infectious Disease (SSGCID) (deposition date: 2021-03-05, release date: 2021-04-14, Last modification date: 2024-11-06) |
Primary citation | McCallum, M.,De Marco, A.,Lempp, F.A.,Tortorici, M.A.,Pinto, D.,Walls, A.C.,Beltramello, M.,Chen, A.,Liu, Z.,Zatta, F.,Zepeda, S.,di Iulio, J.,Bowen, J.E.,Montiel-Ruiz, M.,Zhou, J.,Rosen, L.E.,Bianchi, S.,Guarino, B.,Fregni, C.S.,Abdelnabi, R.,Foo, S.C.,Rothlauf, P.W.,Bloyet, L.M.,Benigni, F.,Cameroni, E.,Neyts, J.,Riva, A.,Snell, G.,Telenti, A.,Whelan, S.P.J.,Virgin, H.W.,Corti, D.,Pizzuto, M.S.,Veesler, D. N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2. Cell, 184:2332-, 2021 Cited by PubMed Abstract: The SARS-CoV-2 spike (S) glycoprotein contains an immunodominant receptor-binding domain (RBD) targeted by most neutralizing antibodies (Abs) in COVID-19 patient plasma. Little is known about neutralizing Abs binding to epitopes outside the RBD and their contribution to protection. Here, we describe 41 human monoclonal Abs (mAbs) derived from memory B cells, which recognize the SARS-CoV-2 S N-terminal domain (NTD) and show that a subset of them neutralize SARS-CoV-2 ultrapotently. We define an antigenic map of the SARS-CoV-2 NTD and identify a supersite (designated site i) recognized by all known NTD-specific neutralizing mAbs. These mAbs inhibit cell-to-cell fusion, activate effector functions, and protect Syrian hamsters from SARS-CoV-2 challenge, albeit selecting escape mutants in some animals. Indeed, several SARS-CoV-2 variants, including the B.1.1.7, B.1.351, and P.1 lineages, harbor frequent mutations within the NTD supersite, suggesting ongoing selective pressure and the importance of NTD-specific neutralizing mAbs for protective immunity and vaccine design. PubMed: 33761326DOI: 10.1016/j.cell.2021.03.028 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.6 Å) |
Structure validation
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