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8FLW

Cryo-EM Structure of PGT145 DU303 Fab in complex with BG505 DS-SOSIP.664

Summary for 8FLW
Entry DOI10.2210/pdb8flw/pdb
EMDB information29288
DescriptorPGT145 DU303 Heavy, PGT145 DU303 Light, Envelope glycoprotein gp41, ... (8 entities in total)
Functional Keywordscd4, hiv-1, sosip, vaccine, immune system, llama, v2 apex, therapeutic, viral protein
Biological sourceHomo sapiens
More
Total number of polymer chains8
Total formula weight285871.07
Authors
Gorman, J.,Kwong, P.D. (deposition date: 2022-12-22, release date: 2023-05-31, Last modification date: 2023-07-26)
Primary citationHolt, G.T.,Gorman, J.,Wang, S.,Lowegard, A.U.,Zhang, B.,Liu, T.,Lin, B.C.,Louder, M.K.,Frenkel, M.S.,McKee, K.,O'Dell, S.,Rawi, R.,Shen, C.H.,Doria-Rose, N.A.,Kwong, P.D.,Donald, B.R.
Improved HIV-1 neutralization breadth and potency of V2-apex antibodies by in silico design.
Cell Rep, 42:112711-112711, 2023
Cited by
PubMed Abstract: Broadly neutralizing antibodies (bNAbs) against HIV can reduce viral transmission in humans, but an effective therapeutic will require unusually high breadth and potency of neutralization. We employ the OSPREY computational protein design software to engineer variants of two apex-directed bNAbs, PGT145 and PG9RSH, resulting in increases in potency of over 100-fold against some viruses. The top designed variants improve neutralization breadth from 39% to 54% at clinically relevant concentrations (IC < 1 μg/mL) and improve median potency (IC) by up to 4-fold over a cross-clade panel of 208 strains. To investigate the mechanisms of improvement, we determine cryoelectron microscopy structures of each variant in complex with the HIV envelope trimer. Surprisingly, we find the largest increases in breadth to be a result of optimizing side-chain interactions with highly variable epitope residues. These results provide insight into mechanisms of neutralization breadth and inform strategies for antibody design and improvement.
PubMed: 37436900
DOI: 10.1016/j.celrep.2023.112711
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.58 Å)
Structure validation

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건을2024-11-06부터공개중

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