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6OO0

Crystal structure of bovine Fab NC-Cow1

Summary for 6OO0
Entry DOI10.2210/pdb6oo0/pdb
DescriptorNC-Cow1 light chain, NC-Cow1 heavy chain, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (4 entities in total)
Functional Keywordshiv-1 broadly neutralizing antibody, viral protein-immune system complex, immune system
Biological sourceBos taurus
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Total number of polymer chains2
Total formula weight52345.92
Authors
Stanfield, R.L.,Wilson, I.A. (deposition date: 2019-04-22, release date: 2020-04-01, Last modification date: 2024-11-13)
Primary citationStanfield, R.L.,Berndsen, Z.T.,Huang, R.,Sok, D.,Warner, G.,Torres, J.L.,Burton, D.R.,Ward, A.B.,Wilson, I.A.,Smider, V.V.
Structural basis of broad HIV neutralization by a vaccine-induced cow antibody.
Sci Adv, 6:eaba0468-eaba0468, 2020
Cited by
PubMed Abstract: Potent broadly neutralizing antibodies (bnAbs) to HIV have been very challenging to elicit by vaccination in wild-type animals. Here, by x-ray crystallography, cryo-electron microscopy, and site-directed mutagenesis, we structurally and functionally elucidate the mode of binding of a potent bnAb (NC-Cow1) elicited in cows by immunization with the HIV envelope (Env) trimer BG505 SOSIP.664. The exceptionally long (60 residues) third complementarity-determining region of the heavy chain (CDR H3) of NC-Cow1 forms a mini domain (knob) on an extended stalk that navigates through the dense glycan shield on Env to target a small footprint on the gp120 CD4 receptor binding site with no contact of the other CDRs to the rest of the Env trimer. These findings illustrate, in molecular detail, how an unusual vaccine-induced cow bnAb to HIV Env can neutralize with high potency and breadth.
PubMed: 32518821
DOI: 10.1126/sciadv.aba0468
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

237735

数据于2025-06-18公开中

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