Insights Into the Structural Peculiarities of The N-terminal and Receptor Binding Domains of the Spike Protein from the SARS-CoV-2 Omicron Variant
Sars-cov-2, Omicron (B.1.1.529, BA.1), N-terminal Domain (NTD), Receptor Binding Domain (RBD), Molecular Dynamics Simulations, COVID-19
Digital Object Identifier (DOI)
Since the new variant of SARS-CoV-2, Omicron (BA.1) has raised serious concerns, it is important to investigate the effects of mutations in the NTD and RBD domains of the spike protein for the development of COVID-19 vaccines. In this study, computational analysis of the Wuhan and Omicron NTDs and RBDs in their unbound and bound states to mAb 4A8 and ACE2 were performed. In addition, the interaction of NTD with antibody and RBD with ACE2 were evaluated in the presence of long glycans. The results show that long glycans at the surface of NTDs can reduce the accessibility of protein epitopes, thereby reducing binding efficiency and neutralizing potency of specific antibodies. Also, our findings indicate that the existence of the long glycans result in increased stability and enhanced affinity of the RBD to ACE2 in the Wuhan and Omicron variant. Key residues that play an important role in increasing the structural stability of the protein were identified using RIN analysis and in the state of interaction with mAb 4A8 and ACE2 through per-residue decomposition analysis. Further, the results of the free energy binding calculation using MM/GBSA method show that the Omicron variant has a higher infectivity than the Wuhan. This study provides a better understanding of the structural changes in the spike protein and can be useful for the development of novel therapeutics.
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Citation / Publisher Attribution
Computers in Biology and Medicine, v. 147, art.105735
Scholar Commons Citation
Bayani, Fatemeh; Hashkavaei, Negin Safaei; Uversky, Vladimir N.; Mozaffari-Jovin, Sina; and Sefidbakht, Yahya, "Insights Into the Structural Peculiarities of The N-terminal and Receptor Binding Domains of the Spike Protein from the SARS-CoV-2 Omicron Variant" (2022). Molecular Medicine Faculty Publications. 1020.