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4HKX

Influenza hemagglutinin in complex with CH67 Fab

Summary for 4HKX
Entry DOI10.2210/pdb4hkx/pdb
Related4HK0 4HK3 4HKB
DescriptorHemagglutinin HA1, CH67 heavy chain, CH67 light chain, ... (5 entities in total)
Functional Keywordsfab fragment, viral protein-immune system complex, viral protein/immune system
Biological sourceInfluenza A virus
More
Total number of polymer chains3
Total formula weight73037.07
Authors
Schmidt, A.G.,Harrison, S.C. (deposition date: 2012-10-15, release date: 2012-11-21, Last modification date: 2024-11-27)
Primary citationSchmidt, A.G.,Xu, H.,Khan, A.R.,O'Donnell, T.,Khurana, S.,King, L.R.,Manischewitz, J.,Golding, H.,Suphaphiphat, P.,Carfi, A.,Settembre, E.C.,Dormitzer, P.R.,Kepler, T.B.,Zhang, R.,Moody, M.A.,Haynes, B.F.,Liao, H.X.,Shaw, D.E.,Harrison, S.C.
Preconfiguration of the antigen-binding site during affinity maturation of a broadly neutralizing influenza virus antibody.
Proc.Natl.Acad.Sci.USA, 110:264-269, 2013
Cited by
PubMed Abstract: Affinity maturation refines a naive B-cell response by selecting mutations in antibody variable domains that enhance antigen binding. We describe a B-cell lineage expressing broadly neutralizing influenza virus antibodies derived from a subject immunized with the 2007 trivalent vaccine. The lineage comprises three mature antibodies, the unmutated common ancestor, and a common intermediate. Their heavy-chain complementarity determining region inserts into the conserved receptor-binding pocket of influenza HA. We show by analysis of structures, binding kinetics and long time-scale molecular dynamics simulations that antibody evolution in this lineage has rigidified the initially flexible heavy-chain complementarity determining region by two nearly independent pathways and that this preconfiguration accounts for most of the affinity gain. The results advance our understanding of strategies for developing more broadly effective influenza vaccines.
PubMed: 23175789
DOI: 10.1073/pnas.1218256109
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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