A shark-derived broadly neutralizing nanobody targeting a highly conserved epitope on the S2 domain of sarbecoviruses

The continuously evolving Omicron subvariants has diminished the effectiveness of almost all RBD-targeted antibodies in neutralizing these subvariants. The development of broad-spectrum neutralizing antibodies is desired for addressing both current and future variants. Here, we identified a shark-derived nanobody, 79C11, that can neutralize all Omicron subvariants tested so far, including BA.1 to JN.1 and KP.2, and exhibits comparable neutralizing potency against SARS-CoV-1 and pangolin coronavirus. Intranasal instillation of 79C11 can effectively prevent the infection of Omicron subvariant XBB in vivo. The designs of multivalent forms of 79C11 further enhance binding and neutralizing activity. Epitope mapping and structure simulation reveal that this nanobody binds to a highly conserved HR1 region in S2 domain of the spikes from all sarbecoviruses, suggesting that a universal vaccine may be designed to target this region for eliciting broadly neutralizing antibody response. This nanobody can also be developed as an intranasally administered prophylactic agent for preventing the infection of current and likely future SARS-CoV-2 variants, as well as other animal derived sarbecoviruses that may infect humans.

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Publication Details

Journal
Journal of Nanobiotechnology
Published
2025-02-15
DOI
https://doi.org/10.1186/s12951-025-03150-2
Citations
8
Primary Topic
Animal Virus Infections Studies
Type
article
Field-Weighted Citation Impact
9.55

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article

A shark-derived broadly neutralizing nanobody targeting a highly conserved epitope on the S2 domain of sarbecoviruses

Xiaoli Xiong, Cuiyun Li, Ping He, Jincun Zhao et al.
8 citations
Journal of Nanobiotechnology
Animal Virus Infections Studies
9.55
article

A shark-derived broadly neutralizing nanobody targeting a highly conserved epitope on the S2 domain of sarbecoviruses

Xiaoli Xiong, Cuiyun Li, Ping He, Jincun Zhao, Banghui Liu, Yongming Huang, Bo Feng, Qian Wang, Ling Chen, Yin Li, Zhengyuan Zhang, Jia Luo, Zhilong Chen, Si Chen, Zhaoyong Zhang, Xuefeng Niu
article en
8 citations

Abstract

The continuously evolving Omicron subvariants has diminished the effectiveness of almost all RBD-targeted antibodies in neutralizing these subvariants. The development of broad-spectrum neutralizing antibodies is desired for addressing both current and future variants. Here, we identified a shark-derived nanobody, 79C11, that can neutralize all Omicron subvariants tested so far, including BA.1 to JN.1 and KP.2, and exhibits comparable neutralizing potency against SARS-CoV-1 and pangolin coronavirus. Intranasal instillation of 79C11 can effectively prevent the infection of Omicron subvariant XBB in vivo. The designs of multivalent forms of 79C11 further enhance binding and neutralizing activity. Epitope mapping and structure simulation reveal that this nanobody binds to a highly conserved HR1 region in S2 domain of the spikes from all sarbecoviruses, suggesting that a universal vaccine may be designed to target this region for eliciting broadly neutralizing antibody response. This nanobody can also be developed as an intranasally administered prophylactic agent for preventing the infection of current and likely future SARS-CoV-2 variants, as well as other animal derived sarbecoviruses that may infect humans.

Journal of NanobiotechnologyVol. 23(1)
Xiamen University (CN), Chinese Academy of Sciences (CN), Guangzhou Institutes of Biomedicine and Health (CN), First Affiliated Hospital of Guangzhou Medical University (CN), Guangzhou Chemistry (China) (CN), State Key Laboratory of Respiratory Disease (CN), Guangzhou Medical University (CN)
National Natural Science Foundation of China
Life below water
Openalex Percentile: Top 2%
Animal Virus Infections Studies
9.55
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