SARS-CoV-2 Omicron variant: Antibody evasion and cryo-EM structure of spike protein–ACE2 complex
University of British Columbia · BC Centre for Disease Control
Abstract
The newly reported Omicron variant is poised to replace Delta as the most prevalent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant across the world. Cryo–electron microscopy (cryo-EM) structural analysis of the Omicron variant spike protein in complex with human angiotensin-converting enzyme 2 (ACE2) reveals new salt bridges and hydrogen bonds formed by mutated residues arginine-493, serine-496, and arginine-498 in the receptor binding domain with ACE2. These interactions appear to compensate for other Omicron mutations such as the substitution of asparagine for lysine at position 417 (K417N) that are known to reduce ACE2 binding affinity, resulting in similar biochemical ACE2 binding…
Citation impact
- FWCI
- 67.54
- Percentile
- 100%
- References
- 43
Authors
9Topics & keywords
- Neutralization
- Antibody
- Chemistry
- Affinities
- Binding affinities
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
- Spike (software development)
- Virology