De novo design of picomolar SARS-CoV-2 miniprotein inhibitors
University of Washington · Washington University in St. Louis · +2 more institutions
Abstract
Miniproteins against SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is decorated with spikes, and viral entry into cells is initiated when these spikes bind to the host angiotensin-converting enzyme 2 (ACE2) receptor. Many monoclonal antibody therapies in development target the spike proteins. Cao et al. designed small, stable proteins that bind tightly to the spike and block it from binding to ACE2. The best designs bind with very high affinity and prevent SARS-CoV-2 infection of mammalian Vero E6 cells. Cryo–electron microscopy shows that the structures of the two most potent inhibitors are nearly identical to the computational models. Unlike antibodies, the miniproteins do not…
Citation impact
- FWCI
- 12.12
- Percentile
- 100%
- References
- 42
Authors
15Topics & keywords
- Ectodomain
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
- Trimer
- Chemistry
- IC50
- Plasma protein binding
- Binding site
- Vero cell
- Good health and well-being