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7RAI

Cryo-EM structure of M4008_N1 Fab in complex with BG505 DS-SOSIP.664 Env trimer

Summary for 7RAI
Entry DOI10.2210/pdb7rai/pdb
EMDB information24362
DescriptorEnvelope glycoprotein gp160, HIV-1 Envelope Glycoprotein BG505 SOSIP.664 gp41, M4008_N1 Fab heavy chain, ... (9 entities in total)
Functional Keywordshiv, envelope, bnab, complex, immune system
Biological sourceHuman immunodeficiency virus 1
More
Total number of polymer chains12
Total formula weight392522.95
Authors
Chan, K.-W.,Kong, X.P. (deposition date: 2021-07-01, release date: 2021-11-17, Last modification date: 2024-11-06)
Primary citationChan, K.W.,Luo, C.C.,Lu, H.,Wu, X.,Kong, X.P.
A site of vulnerability at V3 crown defined by HIV-1 bNAb M4008_N1.
Nat Commun, 12:6464-6464, 2021
Cited by
PubMed Abstract: Identification of vulnerable sites defined by broadly neutralizing antibodies (bNAbs) on HIV-1 envelope (Env) is crucial for vaccine design, and we present here a vulnerable site defined by bNAb M4008_N1, which neutralizes about 40% of a tier-2 virus panel. A 3.2 Å resolution cryo-EM structure of M4008_N1 in complex with BG505 DS-SOSIP reveals a large, shallow protein epitope surface centered at the V3 crown of gp120 and surrounded by key glycans. M4008_N1 interacts with gp120 primarily through its hammerhead CDR H3 to form a β-sheet interaction with the V3 crown hairpin. This makes M4008_N1 compatible with the closed conformation of the prefusion Env trimer, and thus distinct from other known V3 crown mAbs. This mode of bNAb approaching the immunogenic V3 crown in the native Env trimer suggests a strategy for immunogen design targeting this site of vulnerability.
PubMed: 34753944
DOI: 10.1038/s41467-021-26846-z
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.24 Å)
Structure validation

237735

数据于2025-06-18公开中

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