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6VOR

Crystal structure of macaque anti-HIV-1 antibody RM20E1

Summary for 6VOR
Entry DOI10.2210/pdb6vor/pdb
DescriptorRM20E1 Fab heavy chain, RM20E1 Fab light chain, GLYCINE, ... (4 entities in total)
Functional Keywordshiv, antibody, non-human primates, immune system
Biological sourceMacaca mulatta
More
Total number of polymer chains4
Total formula weight97590.91
Authors
Yuan, M.,Wilson, I.A. (deposition date: 2020-01-31, release date: 2020-09-16, Last modification date: 2024-10-30)
Primary citationCottrell, C.A.,van Schooten, J.,Bowman, C.A.,Yuan, M.,Oyen, D.,Shin, M.,Morpurgo, R.,van der Woude, P.,van Breemen, M.,Torres, J.L.,Patel, R.,Gross, J.,Sewall, L.M.,Copps, J.,Ozorowski, G.,Nogal, B.,Sok, D.,Rakasz, E.G.,Labranche, C.,Vigdorovich, V.,Christley, S.,Carnathan, D.G.,Sather, D.N.,Montefiori, D.,Silvestri, G.,Burton, D.R.,Moore, J.P.,Wilson, I.A.,Sanders, R.W.,Ward, A.B.,van Gils, M.J.
Mapping the immunogenic landscape of near-native HIV-1 envelope trimers in non-human primates.
Plos Pathog., 16:e1008753-e1008753, 2020
Cited by
PubMed Abstract: The induction of broad and potent immunity by vaccines is the key focus of research efforts aimed at protecting against HIV-1 infection. Soluble native-like HIV-1 envelope glycoproteins have shown promise as vaccine candidates as they can induce potent autologous neutralizing responses in rabbits and non-human primates. In this study, monoclonal antibodies were isolated and characterized from rhesus macaques immunized with the BG505 SOSIP.664 trimer to better understand vaccine-induced antibody responses. Our studies reveal a diverse landscape of antibodies recognizing immunodominant strain-specific epitopes and non-neutralizing neo-epitopes. Additionally, we isolated a subset of mAbs against an epitope cluster at the gp120-gp41 interface that recognize the highly conserved fusion peptide and the glycan at position 88 and have characteristics akin to several human-derived broadly neutralizing antibodies.
PubMed: 32866207
DOI: 10.1371/journal.ppat.1008753
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.85 Å)
Structure validation

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