5ESV
Crystal Structure of Broadly Neutralizing Antibody CH03, Isolated from Donor CH0219, in Complex with Scaffolded Trimeric HIV-1 Env V1V2 Domain from the Clade C Superinfecting Strain of Donor CAP256.
Summary for 5ESV
Entry DOI | 10.2210/pdb5esv/pdb |
Descriptor | CH03 Heavy Chain, 2-acetamido-2-deoxy-beta-D-glucopyranose, CH03 Light Chain, ... (11 entities in total) |
Functional Keywords | hiv-1, env, v1v2, ch0219, chavi, scaffold, cap256, immune system |
Biological source | Homo sapiens More |
Total number of polymer chains | 9 |
Total formula weight | 230235.51 |
Authors | Gorman, J.,Yang, M.,Kwong, P.D. (deposition date: 2015-11-17, release date: 2015-12-16, Last modification date: 2023-09-27) |
Primary citation | Gorman, J.,Soto, C.,Yang, M.M.,Davenport, T.M.,Guttman, M.,Bailer, R.T.,Chambers, M.,Chuang, G.Y.,DeKosky, B.J.,Doria-Rose, N.A.,Druz, A.,Ernandes, M.J.,Georgiev, I.S.,Jarosinski, M.C.,Joyce, M.G.,Lemmin, T.M.,Leung, S.,Louder, M.K.,McDaniel, J.R.,Narpala, S.,Pancera, M.,Stuckey, J.,Wu, X.,Yang, Y.,Zhang, B.,Zhou, T.,Program, N.C.,Mullikin, J.C.,Baxa, U.,Georgiou, G.,McDermott, A.B.,Bonsignori, M.,Haynes, B.F.,Moore, P.L.,Morris, L.,Lee, K.K.,Shapiro, L.,Mascola, J.R.,Kwong, P.D. Structures of HIV-1 Env V1V2 with broadly neutralizing antibodies reveal commonalities that enable vaccine design. Nat.Struct.Mol.Biol., 23:81-90, 2016 Cited by PubMed Abstract: Broadly neutralizing antibodies (bNAbs) against HIV-1 Env V1V2 arise in multiple donors. However, atomic-level interactions had previously been determined only with antibodies from a single donor, thus making commonalities in recognition uncertain. Here we report the cocrystal structure of V1V2 with antibody CH03 from a second donor and model Env interactions of antibody CAP256-VRC26 from a third donor. These V1V2-directed bNAbs used strand-strand interactions between a protruding antibody loop and a V1V2 strand but differed in their N-glycan recognition. Ontogeny analysis indicated that protruding loops develop early, and glycan interactions mature over time. Altogether, the multidonor information suggested that V1V2-directed bNAbs form an 'extended class', for which we engineered ontogeny-specific antigens: Env trimers with chimeric V1V2s that interacted with inferred ancestor and intermediate antibodies. The ontogeny-based design of vaccine antigens described here may provide a general means for eliciting antibodies of a desired class. PubMed: 26689967DOI: 10.1038/nsmb.3144 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.105 Å) |
Structure validation
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