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6NB8

Crystal structure of anti- SARS-CoV human neutralizing S230 antibody Fab fragment

Summary for 6NB8
Entry DOI10.2210/pdb6nb8/pdb
DescriptorS230 antigen-binding (Fab) fragment, heavy chain, S230 antigen-binding (Fab) fragment, light chain (3 entities in total)
Functional Keywordsfab, coronavirus, sars, glycoprotein, structural genomics, seattle structural genomics center for infectious disease, ssgcid, immune system
Biological sourceHomo sapiens (Human)
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Total number of polymer chains2
Total formula weight48972.53
Authors
Primary citationWalls, A.C.,Xiong, X.,Park, Y.J.,Tortorici, M.A.,Snijder, J.,Quispe, J.,Cameroni, E.,Gopal, R.,Dai, M.,Lanzavecchia, A.,Zambon, M.,Rey, F.A.,Corti, D.,Veesler, D.
Unexpected Receptor Functional Mimicry Elucidates Activation of Coronavirus Fusion.
Cell, 176:1026-1039.e15, 2019
Cited by
PubMed Abstract: Recent outbreaks of severe acute respiratory syndrome and Middle East respiratory syndrome, along with the threat of a future coronavirus-mediated pandemic, underscore the importance of finding ways to combat these viruses. The trimeric spike transmembrane glycoprotein S mediates entry into host cells and is the major target of neutralizing antibodies. To understand the humoral immune response elicited upon natural infections with coronaviruses, we structurally characterized the SARS-CoV and MERS-CoV S glycoproteins in complex with neutralizing antibodies isolated from human survivors. Although the two antibodies studied blocked attachment to the host cell receptor, only the anti-SARS-CoV S antibody triggered fusogenic conformational changes via receptor functional mimicry. These results provide a structural framework for understanding coronavirus neutralization by human antibodies and shed light on activation of coronavirus membrane fusion, which takes place through a receptor-driven ratcheting mechanism.
PubMed: 30712865
DOI: 10.1016/j.cell.2018.12.028
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

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數據於2024-11-13公開中

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