Abstract
Mutations at positions 452 and 486 of the spike glycoprotein receptor
binding domain (RBD) in the SARS-CoV-2 XBC.1 variant were analysed from
the viewpoint of change in hydrophobicity and amino acid charge. A
decrease in hydrophobicity due to mutations at positions 452 and 486 in
the spike glycoprotein was observed, which might affect the infectivity
of the XBC.1 variant. L452M and F486P improve the hACE2-RBD binding
affinity, which might negatively impact the efficacy of vaccines against
SARS-CoV-2, primarily based on spike glycoprotein. Notably, the mutation
L452M in XBC.1 also indicates its probable zoonotic links.