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金纳米粒子上的多磺酸配体作为登革热病毒的杀病毒抗病毒剂。

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

机构信息

Laboratory for nanotechnology, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Prague, Czech Republic.

出版信息

Sci Rep. 2020 Jun 3;10(1):9052. doi: 10.1038/s41598-020-65892-3.

DOI:10.1038/s41598-020-65892-3
PMID:32494059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7271158/
Abstract

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 EC (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 logTCID 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.

摘要

登革热病毒(DENV)每年导致 3.9 亿例感染。感染可能无症状,也可能从轻度发热到严重出血热和休克综合征不等。目前,尚无有效的抗病毒药物或安全的通用疫苗。在本工作中,我们测试了不同的金纳米粒子(AuNP),这些纳米粒子涂有配体,配体的ω端带有带有多个磺酸基的糖。我们旨在识别具有抗病毒特性的化合物,因为这些化合物是不可逆(病毒杀灭)而不是可逆(病毒抑制)抑制。配体的长度、磺酸基团的数量以及糖头基团诱导的空间取向各不相同。我们鉴定了两种候选物,一种是葡萄糖基配体,另一种是乳糖基配体,它们对 DENV-2 的抑制作用具有低 EC(有效浓度,抑制 50%病毒活性)、中等毒性和在肝细胞中的病毒杀灭作用,其半数组织培养感染剂量(TCID50)降低 2.5 和 3.1。分子对接模拟补充了实验结果,表明磺酸基团和 DENV-2 包膜蛋白之间结合的分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/0671fe328562/41598_2020_65892_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/425c18e76daa/41598_2020_65892_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/eb39cc3b9db7/41598_2020_65892_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/0671fe328562/41598_2020_65892_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/425c18e76daa/41598_2020_65892_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/eb39cc3b9db7/41598_2020_65892_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0676/7271158/0671fe328562/41598_2020_65892_Fig3_HTML.jpg

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