Multi-sulfonated ligands on gold nanoparticles as virucidal antiviral for Dengue virus

Autor: Ozgun Kocabiyik, Quy Khac Ong, Danilo Migoni, Dariusz Witt, Valentino Laquintana, Piotr Barski, Francesco Stellacci, Antonella Zacheo, Jan Weber, Nunzio Denora, Giuseppe Felice Mangiatordi, Jan Hodek, Nicoletta Depalo, Silke Krol, Elisabetta Fanizza
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Scientific Reports
Scientific reports (Nature Publishing Group) 10 (2020). doi:10.1038/s41598-020-65892-3
info:cnr-pdr/source/autori:Zacheo, Antonella; Hodek, Jan; Witt, Dariusz; Mangiatordi, Giuseppe F. Elice; Ong, Quy K.; Kocabiyik, Ozgun; Depalo, Nicoletta; Fanizza, Elisabetta; Laquintana, Valentino; Denora, Nunzio; Migoni, Danilo; Barski, Piotr; Stellacci, Francesco; Weber, Jan; Krol, Silke/titolo:Multi-sulfonated ligands on gold nanoparticles as virucidal antiviral for Dengue virus/doi:10.1038%2Fs41598-020-65892-3/rivista:Scientific reports (Nature Publishing Group)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:10
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
ISSN: 2045-2322
Popis: Dengue virus (DENV) causes 390 million infections per year. Infections can be asymptomatic or range from mild fever to severe haemorrhagic fever and shock syndrome. Currently, no effective antivirals or safe universal vaccine is available. In the present work we tested different gold nanoparticles (AuNP) coated with ligands ω-terminated with sugars bearing multiple sulfonate groups. We aimed to identify compounds with antiviral properties due to irreversible (virucidal) rather than reversible (virustatic) inhibition. The ligands varied in length, in number of sulfonated groups as well as their spatial orientation induced by the sugar head groups. We identified two candidates, a glucose- and a lactose-based ligand showing a low EC50 (effective concentration that inhibit 50% of the viral activity) for DENV-2 inhibition, moderate toxicity and a virucidal effect in hepatocytes with titre reduction of Median Tissue Culture Infectious Dose log10TCID50 2.5 and 3.1. Molecular docking simulations complemented the experimental findings suggesting a molecular rationale behind the binding between sulfonated head groups and DENV-2 envelope protein.
Databáze: OpenAIRE