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SARS-CoV-2 B.1.617 Indian variants: are electrostatic potential changes responsible for a higher transmission rate?
Stefano Pascarella; Massimo Ciccozzi; Davide Zella; Martina Bianchi; Francesca Benedetti; Francesco Broccolo; Roberto Cauda; Arnaldo Caruso; Silvia Angeletti; Marta Giovanetti; Antonio Cassone.
Afiliação
  • Stefano Pascarella; Universita di Roma La Sapienza
  • Massimo Ciccozzi; Campus Biomedical University of Rome
  • Davide Zella; Institute of Human Virology- UNiversity of Maryland, Baltimore
  • Martina Bianchi; Universita di Roma la Sapienza
  • Francesca Benedetti; Institute of Human Virology
  • Francesco Broccolo; Universita Bicocca di Milano
  • Roberto Cauda; Universita Cattolica del Sacro Cuore, Rome, Italy
  • Arnaldo Caruso; Universita di Brescia
  • Silvia Angeletti; Policlinico Universitario Campus Biomedico, Rome, Italy
  • Marta Giovanetti; Fundacao Oswaldo Cruz
  • Antonio Cassone; University of Siena
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-445535
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ABSTRACT
Lineage B.1.617+, also known as G/452R.V3, is a recently described SARS-CoV-2 variant under investigation (VUI) firstly identified in October 2020 in India. As of May 2021, three sublineages labelled as B.1.617.1, B.1.617.2 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 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.
Licença
cc_by_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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