4JPV
Crystal structure of broadly and potently neutralizing antibody 3bnc117 in complex with hiv-1 gp120
Summary for 4JPV
Entry DOI | 10.2210/pdb4jpv/pdb |
Related | 3NGB 3SE8 3SE9 4GW4 4JPW |
Descriptor | HIV-1 CLADE A STRAIN 93TH057 GP120 WITH LOOP d AND LOOPD V5 REPLACED FROM HIV STRAIN 3415V1, HEAVY CHAIN OF ANTIBODY 3BNC117, LIGHT CHAIN OF ANTIBODY 3BNC117, ... (7 entities in total) |
Functional Keywords | hiv, gp120, cd4-binding site, 3bnc117, neutralization, vaccine, antibody, envelope protein, viral protein-immune system complex, viral protein/immune system |
Biological source | HUMAN IMMUNODEFICIENCY VIRUS 1 More |
Total number of polymer chains | 3 |
Total formula weight | 89781.44 |
Authors | Zhou, T.,Moquin, S.,Kwong, P.D. (deposition date: 2013-03-19, release date: 2013-04-17, Last modification date: 2024-10-09) |
Primary citation | Klein, F.,Diskin, R.,Scheid, J.F.,Gaebler, C.,Mouquet, H.,Georgiev, I.S.,Pancera, M.,Zhou, T.,Incesu, R.B.,Fu, B.Z.,Gnanapragasam, P.N.,Oliveira, T.Y.,Seaman, M.S.,Kwong, P.D.,Bjorkman, P.J.,Nussenzweig, M.C. Somatic Mutations of the Immunoglobulin Framework Are Generally Required for Broad and Potent HIV-1 Neutralization. Cell(Cambridge,Mass.), 153:126-138, 2013 Cited by PubMed Abstract: Broadly neutralizing antibodies (bNAbs) to HIV-1 can prevent infection and are therefore of great importance for HIV-1 vaccine design. Notably, bNAbs are highly somatically mutated and generated by a fraction of HIV-1-infected individuals several years after infection. Antibodies typically accumulate mutations in the complementarity determining region (CDR) loops, which usually contact the antigen. The CDR loops are scaffolded by canonical framework regions (FWRs) that are both resistant to and less tolerant of mutations. Here, we report that in contrast to most antibodies, including those with limited HIV-1 neutralizing activity, most bNAbs require somatic mutations in their FWRs. Structural and functional analyses reveal that somatic mutations in FWR residues enhance breadth and potency by providing increased flexibility and/or direct antigen contact. Thus, in bNAbs, FWRs play an essential role beyond scaffolding the CDR loops and their unusual contribution to potency and breadth should be considered in HIV-1 vaccine design. PubMed: 23540694DOI: 10.1016/j.cell.2013.03.018 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.827 Å) |
Structure validation
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