8ULU
Cryo-EM structure of the BG505 SOSIPv2 in complex with bNAb 04_A06 and PGDM1400 Fabs
Summary for 8ULU
| Entry DOI | 10.2210/pdb8ulu/pdb |
| EMDB information | 42366 |
| Descriptor | Envelope glycoprotein gp120, alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]alpha-D-mannopyranose-(1-6)-[alpha-D-mannopyranose-(1-3)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (13 entities in total) |
| Functional Keywords | hiv-1, antibody, cd4-binding site, immune complex, viral protein-immune system complex, viral protein/immune system |
| Biological source | Human immunodeficiency virus 1 More |
| Total number of polymer chains | 14 |
| Total formula weight | 434608.80 |
| Authors | DeLaitsch, A.T.,Bjorkman, P.J. (deposition date: 2023-10-16, release date: 2025-04-16, Last modification date: 2025-10-29) |
| Primary citation | Gieselmann, L.,DeLaitsch, A.T.,Rohde, M.,Gruell, H.,Kreer, C.,Ercanoglu, M.S.,Gristick, H.B.,Schommers, P.,Ahmadov, E.,Radford, C.,Mazzolini, A.,Zhang, L.,West Jr., A.P.,Worczinski, J.,Momot, A.,Reichwein, M.L.,Knufer, J.,Stumpf, R.,Mkhize, N.N.,Kaldine, H.,Bhebhe, S.,Deshpande, S.,Giovannoni, F.,Stefanutti, E.,Benigni, F.,Havenar-Daughton, C.,Corti, D.,Kroidl, A.,Adhikari, A.,Nanfack, A.J.,Ambada, G.E.,Duerr, R.,Maganga, L.,William, W.,Ntinginya, N.E.,Wolf, T.,Geldmacher, C.,Hoelscher, M.,Lehmann, C.,Moore, P.L.,Mora, T.,Walczak, A.M.,Gilbert, P.B.,Doria-Rose, N.A.,Huang, Y.,Bloom, J.D.,Seaman, M.S.,Bjorkman, P.J.,Klein, F. Profiling of HIV-1 elite neutralizer cohort reveals a CD4bs bnAb for HIV-1 prevention and therapy. Nat.Immunol., 2025 Cited by PubMed Abstract: Administration of HIV-1 neutralizing antibodies can suppress viremia and prevent infection in vivo. However, clinical use is challenged by envelope diversity and rapid viral escape. Here, we performed single B cell profiling of 32 top HIV-1 elite neutralizers to identify broadly neutralizing antibodies with highest antiviral activity. From 831 expressed monoclonal antibodies, we identified 04_A06, a V1-2-encoded broadly neutralizing antibody to the CD4 binding site with remarkable breadth and potency against multiclade pseudovirus panels (geometric mean half-maximal inhibitory concentration = 0.059 µg ml, breadth = 98.5%, 332 strains). Moreover, 04_A06 was not susceptible to classic CD4 binding site escape variants and maintained full viral suppression in HIV-1-infected humanized mice. Structural analyses revealed an unusually long 11-amino-acid heavy chain insertion that facilitates interprotomer contacts with highly conserved residues on the adjacent gp120 protomer. Finally, 04_A06 demonstrated high activity against contemporaneously circulating viruses from the Antibody-Mediated Prevention trials (geometric mean half-maximal inhibitory concentration = 0.082 µg ml, breadth = 98.4%, 191 virus strains), and in silico modeling for 04_A06LS predicted prevention efficacy of >93%. Thus, 04_A06 will provide unique opportunities for effective treatment and prevention of HIV-1 infection. PubMed: 41053396DOI: 10.1038/s41590-025-02286-5 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.8 Å) |
Structure validation
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