5TFS
Structure of chimeric 02-K Fab, a VRC01-like germline antibody
Summary for 5TFS
Entry DOI | 10.2210/pdb5tfs/pdb |
Related | 5TF1 5TGB |
Descriptor | 02-K Fab Heavy chain, 02-K Fab Light chain, SULFATE ION, ... (4 entities in total) |
Functional Keywords | fab, hiv-1, vrc01, cdrh3, cd4-bs, vh1-2, immune system |
Biological source | Homo sapiens More |
Total number of polymer chains | 2 |
Total formula weight | 46846.11 |
Authors | Pancera, M. (deposition date: 2016-09-26, release date: 2016-11-09, Last modification date: 2024-11-06) |
Primary citation | Yacoob, C.,Pancera, M.,Vigdorovich, V.,Oliver, B.G.,Glenn, J.A.,Feng, J.,Sather, D.N.,McGuire, A.T.,Stamatatos, L. Differences in Allelic Frequency and CDRH3 Region Limit the Engagement of HIV Env Immunogens by Putative VRC01 Neutralizing Antibody Precursors. Cell Rep, 17:1560-1570, 2016 Cited by PubMed Abstract: Elicitation of broadly neutralizing antibodies remains a long-standing goal of HIV vaccine research. Although such antibodies can arise during HIV-1 infection, gaps in our knowledge of their germline, pre-immune precursor forms, as well as on their interaction with viral Env, limit our ability to elicit them through vaccination. Studies of broadly neutralizing antibodies from the VRC01-class provide insight into progenitor B cell receptors (BCRs) that could develop into this class of antibodies. Here, we employed high-throughput heavy chain variable region (VH)/light chain variable region (VL) deep sequencing, combined with biophysical, structural, and modeling antibody analyses, to interrogate circulating potential VRC01-progenitor BCRs in healthy individuals. Our study reveals that not all humans are equally predisposed to generate VRC01-class antibodies, not all predicted progenitor VRC01-expressing B cells can bind to Env, and the CDRH3 region of germline VRC01 antibodies influence their ability to recognize HIV-1. These findings will be critical to the design of optimized immunogens that should consider CDRH3 interactions. PubMed: 27806295DOI: 10.1016/j.celrep.2016.10.017 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.319 Å) |
Structure validation
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