7DEU

Crystal structure of SARS-CoV-2 RBD in complex with a neutralizing antibody scFv

7DEU の概要

• エントリーDOI: 10.2210/pdb7deu/pdb
• 関連するPDBエントリー: 7DEO 7DET
• 分子名称: Spike protein S1, antibody scFv, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
• 機能のキーワード: sars-cov-2, rbd, antibody, viral protein, antiviral protein, viral protein-antiviral protein complex, viral protein/antiviral protein
• 由来する生物種: Severe acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 50755.18

構造登録者

Zhang, Z.,Zhang, G.,Li, X.,Rao, Z.,Guo, Y. (登録日: 2020-11-05, 公開日: 2021-03-31, 最終更新日: 2024-11-13)

主引用文献

Fu, D.,Zhang, G.,Wang, Y.,Zhang, Z.,Hu, H.,Shen, S.,Wu, J.,Li, B.,Li, X.,Fang, Y.,Liu, J.,Wang, Q.,Zhou, Y.,Wang, W.,Li, Y.,Lu, Z.,Wang, X.,Nie, C.,Tian, Y.,Chen, D.,Wang, Y.,Zhou, X.,Wang, Q.,Yu, F.,Zhang, C.,Deng, C.,Zhou, L.,Guan, G.,Shao, N.,Lou, Z.,Deng, F.,Zhang, H.,Chen, X.,Wang, M.,Liu, L.,Rao, Z.,Guo, Y.
Structural basis for SARS-CoV-2 neutralizing antibodies with novel binding epitopes.
Plos Biol., 19:e3001209-e3001209, 2021

PubMed Abstract: The ongoing Coronavirus Disease 2019 (COVID-19) pandemic caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) threatens global public health and economy unprecedentedly, requiring accelerating development of prophylactic and therapeutic interventions. Molecular understanding of neutralizing antibodies (NAbs) would greatly help advance the development of monoclonal antibody (mAb) therapy, as well as the design of next generation recombinant vaccines. Here, we applied H2L2 transgenic mice encoding the human immunoglobulin variable regions, together with a state-of-the-art antibody discovery platform to immunize and isolate NAbs. From a large panel of isolated antibodies, 25 antibodies showed potent neutralizing activities at sub-nanomolar levels by engaging the spike receptor-binding domain (RBD). Importantly, one human NAb, termed PR1077, from the H2L2 platform and 2 humanized NAb, including PR953 and PR961, were further characterized and subjected for subsequent structural analysis. High-resolution X-ray crystallography structures unveiled novel epitopes on the receptor-binding motif (RBM) for PR1077 and PR953, which directly compete with human angiotensin-converting enzyme 2 (hACE2) for binding, and a novel non-blocking epitope on the neighboring site near RBM for PR961. Moreover, we further tested the antiviral efficiency of PR1077 in the Ad5-hACE2 transduction mouse model of COVID-19. A single injection provided potent protection against SARS-CoV-2 infection in either prophylactic or treatment groups. Taken together, these results shed light on the development of mAb-related therapeutic interventions for COVID-19.

PubMed: 33961621
DOI: 10.1371/journal.pbio.3001209

実験手法

X-RAY DIFFRACTION (2.1 Å)