8XKI

A neutralizing nanobody VHH60 against wt SARS-CoV-2

8XKI の概要

• エントリーDOI: 10.2210/pdb8xki/pdb
• EMDBエントリー: 38418
• 分子名称: nanobody VHH60, Spike glycoprotein, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
• 機能のキーワード: covid-19, spike glycoprotein, virus, antibody, viral protein/immune system, viral protein-immune system complex, antiviral protein, antiviral protein-immune system complex, antiviral protein/immune system
• 由来する生物種: synthetic construct; 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 447423.28

構造登録者

Lu, Y.,Guo, H.,Ji, X.,Yang, H. (登録日: 2023-12-23, 公開日: 2024-07-10, 最終更新日: 2025-07-02)

主引用文献

Liu, Q.,Lu, Y.,Cai, C.,Huang, Y.,Zhou, L.,Guan, Y.,Fu, S.,Lin, Y.,Yan, H.,Zhang, Z.,Li, X.,Yang, X.,Yang, H.,Guo, H.,Lan, K.,Chen, Y.,Hou, S.C.,Xiong, Y.
A broad neutralizing nanobody against SARS-CoV-2 engineered from an approved drug.
Cell Death Dis, 15:458-458, 2024

PubMed Abstract: SARS-CoV-2 infection is initiated by Spike glycoprotein binding to the human angiotensin-converting enzyme 2 (ACE2) receptor via its receptor binding domain. Blocking this interaction has been proven to be an effective approach to inhibit virus infection. Here we report the discovery of a neutralizing nanobody named VHH60, which was directly produced from an engineering nanobody library based on a commercialized nanobody within a very short period. VHH60 competes with human ACE2 to bind the receptor binding domain of the Spike protein at S, Sand S as determined by structural analysis, with an affinity of 2.56 nM. It inhibits infections of both ancestral SARS-CoV-2 strain and pseudotyped viruses harboring SARS-CoV-2 wildtype, key mutations or variants at the nanomolar level. Furthermore, VHH60 suppressed SARS-CoV-2 infection and propagation 50-fold better and protected mice from death for twice as long as the control group after SARS-CoV-2 nasal infections in vivo. Therefore, VHH60 is not only a powerful nanobody with a promising profile for disease control but also provides evidence for a highly effective and rapid approach to generating therapeutic nanobodies.

PubMed: 38937437
DOI: 10.1038/s41419-024-06802-7

実験手法

ELECTRON MICROSCOPY (3.2 Å)