7JLK
Crystal structure of glVRC01 Fab in complex with anti-idiotype iv1 scFv
Summary for 7JLK
Entry DOI | 10.2210/pdb7jlk/pdb |
Descriptor | iv1 Heavy Chain, glVRC01 Heavy Chain, glVRC01 Light Chain, ... (9 entities in total) |
Functional Keywords | iv1, glvrc01, fab, scfv, hiv-1, anti-idiotype, immune system |
Biological source | Mus musculus More |
Total number of polymer chains | 4 |
Total formula weight | 77324.98 |
Authors | Weidle, C.,Pancera, M. (deposition date: 2020-07-29, release date: 2021-03-31, Last modification date: 2024-10-09) |
Primary citation | Seydoux, E.,Wan, Y.H.,Feng, J.,Wall, A.,Aljedani, S.,Homad, L.J.,MacCamy, A.J.,Weidle, C.,Gray, M.D.,Brumage, L.,Taylor, J.J.,Pancera, M.,Stamatatos, L.,McGuire, A.T. Development of a VRC01-class germline targeting immunogen derived from anti-idiotypic antibodies. Cell Rep, 35:109084-109084, 2021 Cited by PubMed Abstract: An effective HIV-1 vaccine will likely need to elicit broadly neutralizing antibodies (bNAbs). Broad and potent VRC01-class bNAbs have been isolated from multiple infected individuals, suggesting that they could be reproducibly elicited by vaccination. Several HIV-1 envelope-derived germline-targeting immunogens have been designed to engage naive VRC01-class precursor B cells. However, they also present off-target epitopes that could hinder development of VRC01-class bNAbs. We characterize a panel of anti-idiotypic monoclonal antibodies (ai-mAbs) raised against inferred-germline (iGL) VRC01-class antibodies. By leveraging binding, structural, and B cell sorting data, we engineered a bispecific molecule derived from two ai-mAbs; one specific for VRC01-class heavy chains and one specific for VRC01-class light chains. The bispecific molecule preferentially activates iGL-VRC01 B cells in vitro and induces specific antibody responses in a murine adoptive transfer model with a diverse polyclonal B cell repertoire. This molecule represents an alternative non-envelope-derived germline-targeting immunogen that can selectively activate VRC01-class precursors in vivo. PubMed: 33951425DOI: 10.1016/j.celrep.2021.109084 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.99 Å) |
Structure validation
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