Construction of a Near-Infrared-Activatable Enzyme Platform To Remotely Trigger Intracellular Signal Transduction Using an Upconversion Nanoparticle

ACS Nano. 2015 Jul 28;9(7):7041-51. doi: 10.1021/acsnano.5b01573. Epub 2015 Jul 1.

Abstract

Photoactivatable (caged) bioeffectors provide a way to remotely trigger or disable biochemical pathways in living organisms at a desired time and location with a pulse of light (uncaging), but the phototoxicity of ultraviolet (UV) often limits its application. In this study, we have demonstrated the near-infrared (NIR) photoactivatable enzyme platform using protein kinase A (PKA), an important enzyme in cell biology. We successfully photoactivated PKA using NIR to phosphorylate its substrate, and this induced a downstream cellular response in living cells with high spatiotemporal resolution. In addition, this system allows NIR to selectively activate the caged enzyme immobilized on the nanoparticle surface without activating other caged proteins in the cytosol. This NIR-responsive enzyme-nanoparticle system provides an innovative approach to remote-control proteins and enzymes, which can be used by researchers who need to avoid direct UV irradiation or use UV as a secondary channel to turn on a bioeffector.

Keywords: cellular activity; enzyme; photoactivation; proteins; upconversion nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Cyclic AMP-Dependent Protein Kinases / radiation effects*
  • Enzymes, Immobilized / metabolism
  • Enzymes, Immobilized / radiation effects*
  • Fibroblasts / metabolism
  • Infrared Rays*
  • Nanoparticles / chemistry
  • Nanoparticles / metabolism*
  • Rats
  • Signal Transduction*

Substances

  • Enzymes, Immobilized
  • Cyclic AMP-Dependent Protein Kinases