Topology-Matching Design of an Influenza-Neutralizing Spiky Nanoparticle-Based Inhibitor with a Dual Mode of Action

Angew Chem Int Ed Engl. 2020 Sep 1;59(36):15532-15536. doi: 10.1002/anie.202004832. Epub 2020 Jul 8.

Abstract

In this study, we demonstrate the concept of "topology-matching design" for virus inhibitors. With the current knowledge of influenza A virus (IAV), we designed a nanoparticle-based inhibitor (nano-inhibitor) that has a matched nanotopology to IAV virions and shows heteromultivalent inhibitory effects on hemagglutinin and neuraminidase. The synthesized nano-inhibitor can neutralize the viral particle extracellularly and block its attachment and entry to the host cells. The virus replication was significantly reduced by 6 orders of magnitude in the presence of the reverse designed nano-inhibitors. Even when used 24 hours after the infection, more than 99.999 % inhibition is still achieved, which indicates such a nano-inhibitor might be a potent antiviral for the treatment of influenza infection.

Keywords: antiviral agents; influenza; inhibitors; nanoparticles; topology matching.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Dogs
  • Drug Design*
  • Glycerol / chemistry
  • Glycerol / pharmacology
  • Humans
  • Influenza A virus / drug effects*
  • Influenza, Human / drug therapy*
  • Lactose / analogs & derivatives
  • Lactose / chemistry
  • Lactose / pharmacology
  • Madin Darby Canine Kidney Cells / drug effects
  • Madin Darby Canine Kidney Cells / virology
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Nanoparticles / chemistry*
  • Particle Size
  • Polymers / chemistry
  • Polymers / pharmacology
  • Sialic Acids / chemistry
  • Sialic Acids / pharmacology
  • Surface Properties
  • Virus Replication / drug effects
  • Zanamivir / chemical synthesis
  • Zanamivir / chemistry
  • Zanamivir / pharmacology*

Substances

  • Antiviral Agents
  • Polymers
  • Sialic Acids
  • polyglycerol
  • N-acetylneuraminoyllactose
  • Lactose
  • Zanamivir
  • Glycerol