8GP5
Structure of X18 UFO protomer in complex with F6 Fab VHVL domain
Summary for 8GP5
Entry DOI | 10.2210/pdb8gp5/pdb |
EMDB information | 34190 |
Descriptor | F6 Fab VH domain, F6 Fab VL domain, X18 UFO Env protomer, ... (6 entities in total) |
Functional Keywords | antibody, hiv-1, env protein, complex, viral protein |
Biological source | Homo sapiens More |
Total number of polymer chains | 3 |
Total formula weight | 124228.32 |
Authors | |
Primary citation | Niu, J.,Wang, Q.,Zhao, W.,Meng, B.,Xu, Y.,Zhang, X.,Feng, Y.,Qi, Q.,Hao, Y.,Zhang, X.,Liu, Y.,Xiang, J.,Shao, Y.,Yang, B. Structures and immune recognition of Env trimers from two Asia prevalent HIV-1 CRFs. Nat Commun, 14:4676-4676, 2023 Cited by PubMed Abstract: Structure-guided immunofocusing HIV-1 vaccine design entails a comprehensive understanding of Envs from diverse HIV-1 subtypes, including circulating recombinant forms (CRFs). Here, we present the cryo-EM structures of Envs from two Asia prevalent CRFs (CRF01_AE and CRF07_BC) at 3.0 and 3.5 Å. We compare the structures and glycosylation patterns of Envs from different subtypes and perform cross-clade statistical analyses to reveal the unique features of CRF01_AE V1 region, which are associated with the resistance to certain bNAbs. We also solve a 4.1 Å cryo-EM structure of CRF01_AE Env in complex with F6, the first bNAb from CRF01_AE-infected individuals. F6 recognizes a gp120-gp41 spanning epitope to allosterically destabilize the Env trimer apex and weaken inter-protomer packing, which in turn hinders the receptor binding and induces Env trimer disassembly, demonstrating a dual mechanism of neutralization. These findings broaden our understanding of CRF Envs and shed lights on immunofocusing HIV-1 vaccine design. PubMed: 37542068DOI: 10.1038/s41467-023-40321-x PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (4.05 Å) |
Structure validation
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