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A panel of nanobodies recognizing conserved hidden clefts of all SARS-CoV-2 spike variants including Omicron

Authors :
Ryota Maeda
Junso Fujita
Yoshinobu Konishi
Yasuhiro Kazuma
Hiroyuki Yamazaki
Itsuki Anzai
Tokiko Watanabe
Keishi Yamaguchi
Kazuki Kasai
Kayoko Nagata
Yutaro Yamaoka
Kei Miyakawa
Akihide Ryo
Kotaro Shirakawa
Kei Sato
Fumiaki Makino
Yoshiharu Matsuura
Tsuyoshi Inoue
Akihiro Imura
Keiichi Namba
Akifumi Takaori-Kondo
Source :
Communications Biology. 5
Publication Year :
2022
Publisher :
Springer Science and Business Media LLC, 2022.

Abstract

We are amid the historic coronavirus infectious disease 2019 (COVID-19) pandemic. Imbalances in the accessibility of vaccines, medicines, and diagnostics among countries, regions, and populations, and those in war crises, have been problematic. Nanobodies are small, stable, customizable, and inexpensive to produce. Herein, we present a panel of nanobodies that can detect the spike proteins of five SARS-CoV-2 variants of concern (VOCs) including Omicron. Here we show via ELISA, lateral flow, kinetic, flow cytometric, microscopy, and Western blotting assays that our nanobodies can quantify the spike variants. This panel of nanobodies broadly neutralizes viral infection caused by pseudotyped and authentic SARS-CoV-2 VOCs. Structural analyses show that the P86 clone targets epitopes that are conserved yet unclassified on the receptor-binding domain (RBD) and contacts the N-terminal domain (NTD). Human antibodies rarely access both regions; consequently, the clone buries hidden crevasses of SARS-CoV-2 spike proteins that go undetected by conventional antibodies.<br />新型コロナウイルスを中和するアルパカ抗体 --オミクロンを含む全ての変異株に有効--. 京都大学プレスリリース. 2022-07-14.

Details

ISSN :
23993642
Volume :
5
Database :
OpenAIRE
Journal :
Communications Biology
Accession number :
edsair.doi.dedup.....bd4d65bf766125d283e7066f462fa3d9
Full Text :
https://doi.org/10.1038/s42003-022-03630-3