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3U7Y

Structure of NIH45-46 Fab in complex with gp120 of 93TH057 HIV

3U7Y の概要
エントリーDOI10.2210/pdb3u7y/pdb
関連するPDBエントリー3U7W
分子名称NIH45-46 heavy chain, Ig gamma-1 chain C region, Envelope glycoprotein gp160, NIH45-46 light chain, Ig kappa chain C region, ... (8 entities in total)
機能のキーワードig fold, gp120, anti hiv, glycosylation, viral protein-immune system complex, viral protein/immune system
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数3
化学式量合計90594.78
構造登録者
Diskin, R.,Bjorkman, P.J. (登録日: 2011-10-14, 公開日: 2011-11-16, 最終更新日: 2024-11-20)
主引用文献Diskin, R.,Scheid, J.F.,Marcovecchio, P.M.,West, A.P.,Klein, F.,Gao, H.,Gnanapragasam, P.N.,Abadir, A.,Seaman, M.S.,Nussenzweig, M.C.,Bjorkman, P.J.
Increasing the Potency and Breadth of an HIV Antibody by Using Structure-Based Rational Design.
Science, 334:1289-1293, 2011
Cited by
PubMed Abstract: Antibodies against the CD4 binding site (CD4bs) on the HIV-1 spike protein gp120 can show exceptional potency and breadth. We determined structures of NIH45-46, a more potent clonal variant of VRC01, alone and bound to gp120. Comparisons with VRC01-gp120 revealed that a four-residue insertion in heavy chain complementarity-determining region 3 (CDRH3) contributed to increased interaction between NIH45-46 and the gp120 inner domain, which correlated with enhanced neutralization. We used structure-based design to create NIH45-46(G54W), a single substitution in CDRH2 that increases contact with the gp120 bridging sheet and improves breadth and potency, critical properties for potential clinical use, by an order of magnitude. Together with the NIH45-46-gp120 structure, these results indicate that gp120 inner domain and bridging sheet residues should be included in immunogens to elicit CD4bs antibodies.
PubMed: 22033520
DOI: 10.1126/science.1213782
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.4478 Å)
構造検証レポート
Validation report summary of 3u7y
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-31に公開中

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