Abstract
UNLABELLED: In response to the ongoing COVID-19 pandemic, the quest for coronavirus inhibitors has inspired research on a variety of small proteins beyond conventional antibodies, including robust single-domain antibody fragments, i.e., "nanobodies." Here, we explore the potential of nanobody engineering in the development of antivirals and diagnostic tools. Through fusion of nanobody domains that target distinct binding sites, we engineered multimodular nanobody constructs that neutralize wild-type SARS-CoV-2 and the Alpha and Delta variants at high potency, with IC 50 values as low as 50 pM. Despite simultaneous binding to distinct epitopes, Beta and Omicron variants were more resistant to neutralization by the multimodular nanobodies, which highlights the importance of accounting for antigenic drift in the design of biologics. To further explore the applications of nanobody engineering in outbreak management, we present an assay based on fusions of nanobodies with fragments of NanoLuc luciferase that can detect sub-nanomolar quantities of the SARS-CoV-2 spike protein in a single step. Our work showcases the potential of nanobody engineering to combat emerging infectious diseases.
IMPORTANCE: Nanobodies, small protein binders derived from the camelid antibody, are highly potent inhibitors of respiratory viruses that offer several advantages over conventional antibodies as candidates for specific therapies, including high stability and low production costs. In this work, we leverage the unique properties of nanobodies and apply them as building blocks for new therapeutic and diagnostic tools. We report ultra-potent SARS-CoV-2 inhibition by engineered nanobodies comprising multiple modules in structure-guided combinations and develop nanobodies that carry signal molecules, allowing rapid detection of the SARS-CoV-2 spike protein. Our results highlight the potential of engineered nanobodies in the development of effective countermeasures, both therapeutic and diagnostic, to manage outbreaks of emerging viruses.
Original language | English |
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Article number | e04199-22 |
Journal | Microbiology spectrum |
Volume | 12 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2024 |
MoE publication type | A1 Journal article-refereed |
Funding
This work was funded by the Research Council of Finland (formerly Academy of Finland) (project numbers 342988/IR, 346508/IR, 336492/JTH, 336490/OV, 339510/TS, 338176/VS, and 336495/PS), VEO-European Union\u2019s Horizon 2020 (grant number 874735 to O.V.), the Jane and Aatos Erkko Foundation (to O.V. and V.S.), Sigrid Jus\u00E9lius Foundation (to O.V., V.S., and J.H.), and Helsinki University Hospital Funds (TYH2018322 and TYH2021343 to O.V.).
Keywords
- diagnostics
- nanobody
- protein engineering
- SARS-CoV-2
- virus neutralization
- Antibodies, Neutralizing
- SARS-CoV-2/genetics
- Pandemics
- Humans
- Single-Domain Antibodies/genetics
- COVID-19/diagnosis
- Antibodies, Viral
- Spike Glycoprotein, Coronavirus