8DCE

SARS-CoV-2 Receptor-Binding Domain SPEEDesign Immunogen 1 Bound to C144 scFv

8DCE の概要

• エントリーDOI: 10.2210/pdb8dce/pdb
• 分子名称: C144 scFv, Spike protein S1 (3 entities in total)
• 機能のキーワード: immunogen, antigen, design, vaccine, 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: 2
• 化学式量合計: 52568.63

構造登録者

Tang, W.K.,Tolia, N.H. (登録日: 2022-06-16, 公開日: 2022-06-29, 最終更新日: 2024-11-20)

主引用文献

Dickey, T.H.,Tang, W.K.,Butler, B.,Ouahes, T.,Orr-Gonzalez, S.,Salinas, N.D.,Lambert, L.E.,Tolia, N.H.
Design of the SARS-CoV-2 RBD vaccine antigen improves neutralizing antibody response.
Sci Adv, 8:eabq8276-eabq8276, 2022

PubMed Abstract: The receptor binding domain (RBD) of the SARS-CoV-2 spike protein is the primary target of neutralizing antibodies and is a component of almost all current vaccines. Here, RBD immunogens were created with stabilizing amino acid changes that improve the neutralizing antibody response, as well as characteristics for production, storage, and distribution. A computational design and in vitro screening platform identified three improved immunogens, each with approximately nine amino acid changes relative to the native RBD sequence, and four key changes conserved between immunogens. The changes are adaptable to all vaccine platforms and compatible with mutations in emerging variants of concern. The immunogens elicit higher levels of neutralizing antibodies than native RBD, focus the immune response to structured neutralizing epitopes, and have increased production yields and thermostability. Incorporating these variant-independent amino acid changes in next-generation COVID vaccines may enhance the neutralizing antibody response and lead to longer duration and broader protection.

PubMed: 36103542
DOI: 10.1126/sciadv.abq8276

実験手法

X-RAY DIFFRACTION (2 Å)