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Directed evolution of potent neutralizing nanobodies against SARS-CoV-2 using CDR-swapping mutagenesis
- Source :
- Cell Chemical Biology
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- There is widespread interest in facile methods for generating potent neutralizing antibodies, nanobodies, and other affinity proteins against SARS-CoV-2 and related viruses to address current and future pandemics. While isolating antibodies from animals and humans are proven approaches, these methods are limited to the affinities, specificities, and functional activities of antibodies generated by the immune system. Here we report a surprisingly simple directed evolution method for generating nanobodies with high affinities and neutralization activities against SARS-CoV-2. We demonstrate that complementarity-determining region swapping between low-affinity lead nanobodies, which we discovered unintentionally but find is simple to implement systematically, results in matured nanobodies with unusually large increases in affinity. Importantly, the matured nanobodies potently neutralize both SARS-CoV-2 pseudovirus and live virus, and possess drug-like biophysical properties. We expect that our methods will improve in vitro nanobody discovery and accelerate the generation of potent neutralizing nanobodies against diverse coronaviruses.<br />Graphical abstract<br />Zupancic et al. report potent neutralizing nanobodies against SARS-CoV-2. They demonstrate an approach that involves swapping the complementarity-determining regions of low-affinity clones to generate matured nanobodies with large increases in affinity and neutralization activity.
- Subjects :
- Resource
Clinical Biochemistry
ACE2
Mutagenesis (molecular biology technique)
Computational biology
Complementarity determining region
yeast
01 natural sciences
Biochemistry
Epitope
Neutralization
RBD
Drug Discovery
Molecular Biology
Pharmacology
biology
maturation
010405 organic chemistry
HEK 293 cells
COVID-19
spike
neutralization
Directed evolution
0104 chemical sciences
3. Good health
nanobody
biology.protein
Vero cell
Molecular Medicine
affinity
receptor-binding domain
Antibody
Subjects
Details
- ISSN :
- 24519456
- Volume :
- 28
- Database :
- OpenAIRE
- Journal :
- Cell Chemical Biology
- Accession number :
- edsair.doi.dedup.....5bf2244abc9adc4a7b535c1ac315d89d
- Full Text :
- https://doi.org/10.1016/j.chembiol.2021.05.019