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8SGA

Crystal structure of 770E11, a monoclonal antibody isolated from a human Epstein-Barr virus seropositive donor

Summary for 8SGA
Entry DOI10.2210/pdb8sga/pdb
Descriptor770E11 Fab light chain, 770E11 Fab heavy chain, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
Functional Keywordsmonoclonal antibody, epstein-barr virus, human protein, immune system
Biological sourceHomo sapiens
More
Total number of polymer chains2
Total formula weight46697.03
Authors
Chen, W.H.,Jensen, J.L.,Joyce, M.G. (deposition date: 2023-04-12, release date: 2024-04-17, Last modification date: 2025-02-26)
Primary citationJoyce, M.G.,Bu, W.,Chen, W.H.,Gillespie, R.A.,Andrews, S.F.,Wheatley, A.K.,Tsybovsky, Y.,Jensen, J.L.,Stephens, T.,Prabhakaran, M.,Fisher, B.E.,Narpala, S.R.,Bagchi, M.,McDermott, A.B.,Nabel, G.J.,Kwong, P.D.,Mascola, J.R.,Cohen, J.I.,Kanekiyo, M.
Structural basis for complement receptor engagement and virus neutralization through Epstein-Barr virus gp350.
Immunity, 58:295-, 2025
Cited by
PubMed Abstract: Epstein-Barr virus (EBV) causes infectious mononucleosis and is associated with malignancies in humans. Viral infection of B cells is initiated by the viral glycoprotein 350 (gp350) binding to complement receptor 2 (CR2). Despite decades of effort, no vaccines or curative agents have been developed, partly due to lack of atomic-level understanding of the virus-host interface. Here, we determined the 1.7 Å structure of gp350 in complex with CR2. CR2 binding of gp350 utilized the same set of Arg residues required for recognition of its natural ligand, complement C3d. We further determined the structures of gp350 in complex with three potently neutralizing antibodies (nAbs) obtained from vaccinated macaques and EBV-infected individuals. Like the CR2 interaction, these nAbs targeted the acidic pocket within the CR2-binding site on gp350 using Arg residues. Our results illustrate two axes of molecular mimicry-gp350 versus C3d and CR2 versus EBV nAbs-offering insights for EBV vaccines and therapeutics development.
PubMed: 39909035
DOI: 10.1016/j.immuni.2025.01.010
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

237735

数据于2025-06-18公开中

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