Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein-protein interaction module

Nat Commun. 2016 Jul 22:7:12277. doi: 10.1038/ncomms12277.

Abstract

Nanoparticle-mediated delivery of functional macromolecules is a promising method for treating a variety of human diseases. Among nanoparticles, cell-derived exosomes have recently been highlighted as a new therapeutic strategy for the in vivo delivery of nucleotides and chemical drugs. Here we describe a new tool for intracellular delivery of target proteins, named 'exosomes for protein loading via optically reversible protein-protein interactions' (EXPLORs). By integrating a reversible protein-protein interaction module controlled by blue light with the endogenous process of exosome biogenesis, we are able to successfully load cargo proteins into newly generated exosomes. Treatment with protein-loaded EXPLORs is shown to significantly increase intracellular levels of cargo proteins and their function in recipient cells in vitro and in vivo. These results clearly indicate the potential of EXPLORs as a mechanism for the efficient intracellular transfer of protein-based therapeutics into recipient cells and tissues.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arabidopsis Proteins
  • Basic Helix-Loop-Helix Transcription Factors
  • Cryptochromes
  • Drug Delivery Systems*
  • Exosomes*
  • Genetic Engineering*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Mice, Transgenic
  • Optical Imaging*
  • Recombinant Proteins / administration & dosage*

Substances

  • Arabidopsis Proteins
  • Basic Helix-Loop-Helix Transcription Factors
  • CIB1 protein, Arabidopsis
  • CRY2 protein, Arabidopsis
  • Cryptochromes
  • Recombinant Proteins