Engineering of Janus-Like Dendrimers with Peptides Derived from Glycoproteins of Herpes Simplex Virus Type 1: Toward a Versatile and Novel Antiviral Platform

Int J Mol Sci. 2021 Jun 17;22(12):6488. doi: 10.3390/ijms22126488.

Abstract

Novel antiviral nanotherapeutics, which may inactivate the virus and block it from entering host cells, represent an important challenge to face viral global health emergencies around the world. Using a combination of bioorthogonal copper-catalyzed 1,3-dipolar alkyne/azide cycloaddition (CuAAC) and photoinitiated thiol-ene coupling, monofunctional and bifunctional peptidodendrimer conjugates were obtained. The conjugates are biocompatible and demonstrate no toxicity to cells at biologically relevant concentrations. Furthermore, the orthogonal addition of multiple copies of two different antiviral peptides on the surface of a single dendrimer allowed the resulting bioconjugates to inhibit Herpes simplex virus type 1 at both the early and the late stages of the infection process. The presented work builds on further improving this attractive design to obtain a new class of therapeutics.

Keywords: antiviral compounds; dendrimers; peptides.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • CHO Cells
  • Cell Line
  • Cell Survival / drug effects
  • Chemical Phenomena
  • Chemistry Techniques, Synthetic
  • Chromatography, High Pressure Liquid
  • Cricetulus
  • Dendrimers / chemistry
  • Dendrimers / pharmacology*
  • Glycoproteins* / chemistry
  • Herpesvirus 1, Human* / metabolism
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Peptides / chemistry
  • Peptides / pharmacology*
  • Spectrum Analysis
  • Viral Proteins* / chemistry

Substances

  • Antiviral Agents
  • Dendrimers
  • Glycoproteins
  • Peptides
  • Viral Proteins