TY - JOUR
T1 - SARS-CoV-2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate?
AU - Pascarella, Stefano
AU - Ciccozzi, Massimo
AU - Zella, Davide
AU - Bianchi, Martina
AU - Benedetti, Francesca
AU - Benvenuto, Domenico
AU - Broccolo, Francesco
AU - Cauda, Roberto
AU - Caruso, Arnaldo
AU - Angeletti, Silvia
AU - Giovanetti, Marta
AU - Cassone, Antonio
PY - 2021
Y1 - 2021
N2 - 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.
AB - 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.
KW - B.1.617 δ and κ variants
KW - COVID-19
KW - Humans
KW - Mutation
KW - Protein Structure, Tertiary
KW - SARS-CoV-2
KW - Spike Glycoprotein, Coronavirus
KW - Static Electricity
KW - electrostatics potential changes
KW - B.1.617 δ and κ variants
KW - COVID-19
KW - Humans
KW - Mutation
KW - Protein Structure, Tertiary
KW - SARS-CoV-2
KW - Spike Glycoprotein, Coronavirus
KW - Static Electricity
KW - electrostatics potential changes
UR - http://hdl.handle.net/10807/201610
U2 - 10.1002/jmv.27210
DO - 10.1002/jmv.27210
M3 - Article
SN - 0146-6615
VL - 93
SP - 6551
EP - 6556
JO - Journal of Medical Virology
JF - Journal of Medical Virology
ER -