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6XWI

Solution NMR structure of the S0_2.126 designed protein

6XWI の概要
エントリーDOI10.2210/pdb6xwi/pdb
NMR情報BMRB: 34481
分子名称S0_2.126 (1 entity in total)
機能のキーワードdesigned protein, de novo protein
由来する生物種synthetic construct
タンパク質・核酸の鎖数1
化学式量合計8209.47
構造登録者
Abriata, L.A. (登録日: 2020-01-23, 公開日: 2020-04-15, 最終更新日: 2024-11-13)
主引用文献Sesterhenn, F.,Yang, C.,Bonet, J.,Cramer, J.T.,Wen, X.,Wang, Y.,Chiang, C.I.,Abriata, L.A.,Kucharska, I.,Castoro, G.,Vollers, S.S.,Galloux, M.,Dheilly, E.,Rosset, S.,Corthesy, P.,Georgeon, S.,Villard, M.,Richard, C.A.,Descamps, D.,Delgado, T.,Oricchio, E.,Rameix-Welti, M.A.,Mas, V.,Ervin, S.,Eleouet, J.F.,Riffault, S.,Bates, J.T.,Julien, J.P.,Li, Y.,Jardetzky, T.,Krey, T.,Correia, B.E.
De novo protein design enables the precise induction of RSV-neutralizing antibodies.
Science, 368:-, 2020
Cited by
PubMed Abstract: De novo protein design has been successful in expanding the natural protein repertoire. However, most de novo proteins lack biological function, presenting a major methodological challenge. In vaccinology, the induction of precise antibody responses remains a cornerstone for next-generation vaccines. Here, we present a protein design algorithm called TopoBuilder, with which we engineered epitope-focused immunogens displaying complex structural motifs. In both mice and nonhuman primates, cocktails of three de novo-designed immunogens induced robust neutralizing responses against the respiratory syncytial virus. Furthermore, the immunogens refocused preexisting antibody responses toward defined neutralization epitopes. Overall, our design approach opens the possibility of targeting specific epitopes for the development of vaccines and therapeutic antibodies and, more generally, will be applicable to the design of de novo proteins displaying complex functional motifs.
PubMed: 32409444
DOI: 10.1126/science.aay5051
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 6xwi
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2026-04-22に公開中

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