Structural and functional characterizations of infectivity and immune evasion of SARS-CoV-2 Omicron
Chinese Academy of Sciences · Institute of Biophysics · +3 more institutions
Abstract
The SARS-CoV-2 Omicron variant with increased fitness is spreading rapidly worldwide. Analysis of cryo-EM structures of the spike (S) from Omicron reveals amino acid substitutions forging interactions that stably maintain an active conformation for receptor recognition. The relatively more compact domain organization confers improved stability and enhances attachment but compromises the efficiency of the viral fusion step. Alterations in local conformation, charge, and hydrophobic microenvironments underpin the modulation of the epitopes such that they are not recognized by most NTD- and RBD-antibodies, facilitating viral immune escape. Structure of the Omicron S bound with human ACE2, together with the…
Citation impact
- FWCI
- 45.56
- Percentile
- 100%
- References
- 64
Authors
23- ZCZhen Cui
Chinese Academy of Sciences, Institute of Biophysics, University of Chinese Academy of Sciences
- PLPan Liu
Chinese Academy of Sciences, Institute of Biophysics, University of Chinese Academy of Sciences
- NWNan Wang
Chinese Academy of Sciences, Institute of Biophysics
- LWLei Wang
Chinese Academy of Sciences, Institute of Biophysics, University of Chinese Academy of Sciences
- KFKaiyue Fan
Chinese Academy of Sciences, Institute of Biophysics, University of Chinese Academy of Sciences
Topics & keywords
- Biology
- Infectivity
- Epitope
- Immune system
- Immune escape
- Peptide sequence
- Virology
- Antibody
- Life in Land
Funding
- CAChinese Academy of SciencesAwards: YSBR-010, XDB29010000
- MOMinistry of Science and Technology of the People's Republic of ChinaAwards: EKPG21-09, CPL-1233
- CAChinese Academy of Medical Sciences
- BMBeijing Municipal Science and Technology CommissionAward: Z201100005420017
- ZPZhejiang Provincial Ten Thousand Plan for Young Top Talents
- NKNational Key Research and Development Program of ChinaAwards: 2018YFA0900801, 2020YFA0707500