7SWD

Structure of EBOV GP lacking the mucin-like domain with 1C11 scFv and 1C3 Fab bound

Summary for 7SWD

• Entry DOI: 10.2210/pdb7swd/pdb
• EMDB information: 25471
• Descriptor: Virion spike glycoprotein GP1, Virion spike glycoprotein GP2, 1C11 scFv, ... (6 entities in total)
• Functional Keywords: viral protein, glycoprotein, immune system, antibody, ebola virus, viral protein-immune system complex, viral protein/immune system
• Biological source: Ebola virus - Gabon (1994-1997); More
• Total number of polymer chains: 11
• Total formula weight: 234204.04

Authors

Milligan, J.C.,Yu, X.,Saphire, E.O. (deposition date: 2021-11-19, release date: 2022-04-06, Last modification date: 2024-10-30)

Primary citation

Milligan, J.C.,Davis, C.W.,Yu, X.,Ilinykh, P.A.,Huang, K.,Halfmann, P.J.,Cross, R.W.,Borisevich, V.,Agans, K.N.,Geisbert, J.B.,Chennareddy, C.,Goff, A.J.,Piper, A.E.,Hui, S.,Shaffer, K.C.L.,Buck, T.,Heinrich, M.L.,Branco, L.M.,Crozier, I.,Holbrook, M.R.,Kuhn, J.H.,Kawaoka, Y.,Glass, P.J.,Bukreyev, A.,Geisbert, T.W.,Worwa, G.,Ahmed, R.,Saphire, E.O.
Asymmetric and non-stoichiometric glycoprotein recognition by two distinct antibodies results in broad protection against ebolaviruses.
Cell, 185:995-1007.e18, 2022

PubMed Abstract: Several ebolaviruses cause outbreaks of severe disease. Vaccines and monoclonal antibody cocktails are available to treat Ebola virus (EBOV) infections, but not Sudan virus (SUDV) or other ebolaviruses. Current cocktails contain antibodies that cross-react with the secreted soluble glycoprotein (sGP) that absorbs virus-neutralizing antibodies. By sorting memory B cells from EBOV infection survivors, we isolated two broadly reactive anti-GP monoclonal antibodies, 1C3 and 1C11, that potently neutralize, protect rodents from disease, and lack sGP cross-reactivity. Both antibodies recognize quaternary epitopes in trimeric ebolavirus GP. 1C11 bridges adjacent protomers via the fusion loop. 1C3 has a tripartite epitope in the center of the trimer apex. One 1C3 antigen-binding fragment anchors simultaneously to the three receptor-binding sites in the GP trimer, and separate 1C3 paratope regions interact differently with identical residues on the three protomers. A cocktail of both antibodies completely protected nonhuman primates from EBOV and SUDV infections, indicating their potential clinical value.

PubMed: 35303429
DOI: 10.1016/j.cell.2022.02.023

Experimental method

ELECTRON MICROSCOPY (3.59 Å)