7Z3A
AMC009 SOSIPv5.2 in complex with Fabs ACS101 and ACS124
This is a non-PDB format compatible entry.
Summary for 7Z3A
| Entry DOI | 10.2210/pdb7z3a/pdb |
| EMDB information | 14474 |
| Descriptor | AMC009 SOSIPv5.2 envelope glycoprotein gp120, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-6)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (11 entities in total) |
| Functional Keywords | hiv-1, antibodies, cd4-binding site, gp41-gp120 interface, viral protein |
| Biological source | Human immunodeficiency virus 1 More |
| Total number of polymer chains | 16 |
| Total formula weight | 374065.69 |
| Authors | van Schooten, J.,Ward, A. (deposition date: 2022-03-02, release date: 2022-08-10, Last modification date: 2024-11-06) |
| Primary citation | van Schooten, J.,Farokhi, E.,Schorcht, A.,van den Kerkhof, T.L.G.M.,Gao, H.,van der Woude, P.,Burger, J.A.,Meesters, T.G.R.,Bijl, T.,Ghalaiyini, R.,Turner, H.L.,Dorning, J.,van Schaik, B.D.C.,van Kampen, A.H.C.,Labranche, C.C.,Stanfield, R.L.,Sok, D.,Montefiori, D.C.,Burton, D.R.,Seaman, M.S.,Ozorowski, G.,Wilson, I.A.,Sanders, R.W.,Ward, A.B.,van Gils, M.J. Identification of IOMA-class neutralizing antibodies targeting the CD4-binding site on the HIV-1 envelope glycoprotein. Nat Commun, 13:4515-4515, 2022 Cited by PubMed Abstract: A major goal of current HIV-1 vaccine design efforts is to induce broadly neutralizing antibodies (bNAbs). The VH1-2-derived bNAb IOMA directed to the CD4-binding site of the HIV-1 envelope glycoprotein is of interest because, unlike the better-known VH1-2-derived VRC01-class bNAbs, it does not require a rare short light chain complementarity-determining region 3 (CDRL3). Here, we describe three IOMA-class NAbs, ACS101-103, with up to 37% breadth, that share many characteristics with IOMA, including an average-length CDRL3. Cryo-electron microscopy revealed that ACS101 shares interactions with those observed with other VH1-2 and VH1-46-class bNAbs, but exhibits a unique binding mode to residues in loop D. Analysis of longitudinal sequences from the patient suggests that a transmitter/founder-virus lacking the N276 glycan might have initiated the development of these NAbs. Together these data strengthen the rationale for germline-targeting vaccination strategies to induce IOMA-class bNAbs and provide a wealth of sequence and structural information to support such strategies. PubMed: 35922441DOI: 10.1038/s41467-022-32208-0 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.95 Å) |
Structure validation
Download full validation report
