Mitochondria-Targeting, Intracellular Delivery of Native Proteins Using Biodegradable Silica Nanoparticles

Angew Chem Int Ed Engl. 2019 Jun 3;58(23):7657-7661. doi: 10.1002/anie.201901699. Epub 2019 May 2.

Abstract

Mitochondria are key organelles in mammalian cells whose dysfunction is linked to various diseases. Drugs targeting mitochondrial proteins provide a highly promising strategy for potential therapeutics. Methods for the delivery of small-molecule drugs to the mitochondria are available, but these are not suitable for macromolecules, such as proteins. Herein, we report the delivery of native proteins and antibodies to the mitochondria using biodegradable silica nanoparticles (BS-NPs). The modification of the nanoparticle surface with triphenylphosphonium (TPP) and cell-penetrating poly(disulfide)s (CPD) facilitated their rapid intracellular uptake with minimal endolysosomal trapping, providing sufficient time for effective mitochondrial localization followed by glutathione-triggered biodegradation and of native, functional proteins into the mitochondria.

Keywords: antibody delivery; biodegradable; glutathione; mitochondrial targeting; protein delivery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal / immunology
  • Disulfides / chemistry
  • Drug Carriers / chemistry*
  • Drug Delivery Systems*
  • Electron Transport Complex IV / immunology
  • Glutathione / metabolism
  • HeLa Cells
  • Hep G2 Cells
  • Humans
  • Mitochondria / metabolism*
  • Monoamine Oxidase / administration & dosage*
  • Nanoparticles / administration & dosage*
  • Nanoparticles / chemistry
  • Polymers / chemistry
  • Silicon Dioxide / chemistry*

Substances

  • Antibodies, Monoclonal
  • Disulfides
  • Drug Carriers
  • Polymers
  • Silicon Dioxide
  • Monoamine Oxidase
  • cytochrome C oxidase subunit II
  • Electron Transport Complex IV
  • Glutathione