4JPI
Crystal structure of a putative VRC01 germline precursor Fab
Summary for 4JPI
| Entry DOI | 10.2210/pdb4jpi/pdb |
| Related | 4JPJ 4JPK |
| Descriptor | Putative VRC01 germline Fab heavy chain, Putative VRC01 germline Fab light chain, GLYCEROL, ... (4 entities in total) |
| Functional Keywords | anti-hiv-1, gp120, cd4 binding site-targeting, vrc01 broadly neutralizing antibody, immune system |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 4 |
| Total formula weight | 99646.74 |
| Authors | Julien, J.-P.,Diwanji, D.C.,Jardine, J.,Schief, W.R.,Wilson, I.A. (deposition date: 2013-03-19, release date: 2013-04-10, Last modification date: 2024-11-20) |
| Primary citation | Jardine, J.,Julien, J.P.,Menis, S.,Ota, T.,Kalyuzhniy, O.,McGuire, A.,Sok, D.,Huang, P.S.,MacPherson, S.,Jones, M.,Nieusma, T.,Mathison, J.,Baker, D.,Ward, A.B.,Burton, D.R.,Stamatatos, L.,Nemazee, D.,Wilson, I.A.,Schief, W.R. Rational HIV immunogen design to target specific germline B cell receptors. Science, 340:711-716, 2013 Cited by PubMed Abstract: Vaccine development to induce broadly neutralizing antibodies (bNAbs) against HIV-1 is a global health priority. Potent VRC01-class bNAbs against the CD4 binding site of HIV gp120 have been isolated from HIV-1-infected individuals; however, such bNAbs have not been induced by vaccination. Wild-type gp120 proteins lack detectable affinity for predicted germline precursors of VRC01-class bNAbs, making them poor immunogens to prime a VRC01-class response. We employed computation-guided, in vitro screening to engineer a germline-targeting gp120 outer domain immunogen that binds to multiple VRC01-class bNAbs and germline precursors, and elucidated germline binding crystallographically. When multimerized on nanoparticles, this immunogen (eOD-GT6) activates germline and mature VRC01-class B cells. Thus, eOD-GT6 nanoparticles have promise as a vaccine prime. In principle, germline-targeting strategies could be applied to other epitopes and pathogens. PubMed: 23539181DOI: 10.1126/science.1234150 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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