7UOT

Native Lassa glycoprotein in complex with neutralizing antibodies 8.9F and 37.2D

7UOT の概要

• エントリーDOI: 10.2210/pdb7uot/pdb
• EMDBエントリー: 26653
• 分子名称: Glycoprotein G1, alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (14 entities in total)
• 機能のキーワード: lassa virus, neutralizing antibody, n-linked glycans complex, viral protein, viral protein-immune system complex, viral protein/immune system
• 由来する生物種: Lassa virus; 詳細
• タンパク質・核酸の鎖数: 14
• 化学式量合計: 292032.54

構造登録者

Li, H.,Saphire, E.O. (登録日: 2022-04-13, 公開日: 2022-11-02, 最終更新日: 2025-05-28)

主引用文献

Li, H.,Buck, T.,Zandonatti, M.,Yin, J.,Moon-Walker, A.,Fang, J.,Koval, A.,Heinrich, M.L.,Rowland, M.M.,Diaz Avalos, R.,Schendel, S.L.,Parekh, D.,Zyla, D.,Enriquez, A.,Harkins, S.,Sullivan, B.,Smith, V.,Chukwudozie, O.,Watanabe, R.,Robinson, J.E.,Garry, R.F.,Branco, L.M.,Hastie, K.M.,Saphire, E.O.
A cocktail of protective antibodies subverts the dense glycan shield of Lassa virus.
Sci Transl Med, 14:eabq0991-eabq0991, 2022

PubMed Abstract: Developing potent therapeutics and effective vaccines are the ultimate goals in controlling infectious diseases. Lassa virus (LASV), the causative pathogen of Lassa fever (LF), infects hundreds of thousands annually, but effective antivirals or vaccines against LASV infection are still lacking. Furthermore, neutralizing antibodies against LASV are rare. Here, we describe biochemical analyses and high-resolution cryo-electron microscopy structures of a therapeutic cocktail of three broadly protective antibodies that target the LASV glycoprotein complex (GPC), previously identified from survivors of multiple LASV infections. Structural and mechanistic analyses reveal compatible neutralizing epitopes and complementary neutralization mechanisms that offer high potency, broad range, and resistance to escape. These antibodies either circumvent or exploit specific glycans comprising the extensive glycan shield of GPC. Further, they require mammalian glycosylation, native GPC cleavage, and proper GPC trimerization. These findings guided engineering of a next-generation GPC antigen suitable for future neutralizing antibody and vaccine discovery. Together, these results explain protective mechanisms of rare, broad, and potent antibodies and identify a strategy for the rational design of therapeutic modalities against LF and related infectious diseases.

PubMed: 36288283
DOI: 10.1126/scitranslmed.abq0991

実験手法

ELECTRON MICROSCOPY (2.77 Å)