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Spatio-Temporal Photoactivation of Cytotoxic Proteins.

Raquel Cruz-SamperioRobert J MartLouis Y P LukYu-Hsuan TsaiArwyn T JonesRudolf K Allemann
Published in: Chembiochem : a European journal of chemical biology (2022)
Protein therapeutics offer exquisite selectivity in targeting cellular processes and behaviors, but are rarely used against non-cell surface targets due to their poor cellular uptake. While cell-penetrating peptides can be used to deliver recombinant proteins to the cytosol, it is generally difficult to selectively deliver active proteins to target cells. Here, we report a recombinantly produced, intracellular protein delivery and targeting platform that uses a photocaged intein to regulate the spatio-temporal activation of protein activity in selected cells upon irradiation with light. The platform was successfully demonstrated for two cytotoxic proteins to selectively kill cancer cells after photoactivation of intein splicing. This platform can generically be applied to any protein whose activity can be disrupted by a fused intein, allowing it to underpin a wide variety of future protein therapeutics.
Keyphrases
  • protein protein
  • induced apoptosis
  • amino acid
  • binding protein
  • small molecule
  • cell surface
  • high throughput
  • stem cells
  • cell proliferation
  • cell therapy
  • mesenchymal stem cells
  • radiation therapy
  • functional connectivity