Journal of Medical Virology · 2021 · 99 citations · 25 references
Life SciencesBiologyInfectious DiseasesMolecular EvolutionMolecular VirologyVirologyElectrostatics In BiomoleculesEmerging Viral DiseasesProtein StructureViral InfectionsAmino AcidsCodon 13 MutationsElectrostatic Potential ProfileElectrostatic Surface PotentialMolecular Electrostatic PotentialSars-cov-2 InfectionVariants Of ConcernViral Spike Proteins
Lineage B.1.617+, also known as G/452R.V3 and now denoted by WHO with the Greek letters δ and κ, is a recently described SARS-CoV-2 variant under investigation first identified in October 2020 in India. As of May 2021, three sublineages labeled as B.1.617.1 (κ), B.1.617.2 (δ), and B.1.617.3 have been already identified, and their potential impact on the current pandemic is being studied. This variant has 13 amino acid changes, three in its spike protein, which are currently of particular concern: E484Q, L452R, and P681R. Here, we report a major effect of the mutations characterizing this lineage, represented by a marked alteration of the surface electrostatic potential (EP) of the receptor-binding domain (RBD) of the spike protein. Enhanced RBD-EP is particularly noticeable in the B.1.617.2 (δ) sublineage, which shows multiple replacements of neutral or negatively charged amino acids with positively charged amino acids. We here hypothesize that this EP change can favor the interaction between the B.1.617+ RBD and the negatively charged ACE2, thus conferring a potential increase in the virus transmission.
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Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor
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