Three-dimensional protein networks assembled by two-photon activation

Angew Chem Int Ed Engl. 2014 May 26;53(22):5680-4. doi: 10.1002/anie.201309930. Epub 2014 Apr 11.

Abstract

Spatial and temporal control over chemical and biological processes plays a key role in life and material sciences. Here we synthesized a two-photon-activatable glutathione (GSH) to trigger the interaction with glutathione S-transferase (GST) by light at superior spatiotemporal resolution. The compound shows fast and well-confined photoconversion into the bioactive GSH, which is free to interact with GST-tagged proteins. The GSH/GST interaction can be phototriggered, changing its affinity over several orders of magnitude into the nanomolar range. Multiplexed three-dimensional (3D) protein networks are simultaneously generated in situ through two-photon fs-pulsed laser-scanning excitation. The two-photon activation facilitates the three-dimensional assembly of protein structures in real time at hitherto unseen resolution in time and space, thus opening up new applications far beyond the presented examples.

Keywords: immobilization; photochemistry; protein-protein interactions; surface chemistry; two-photon activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electron Transport
  • Fluorescence Resonance Energy Transfer
  • Glutathione / chemistry
  • Glutathione / metabolism
  • Glutathione Transferase / metabolism*
  • Light
  • Photons
  • Protein Interaction Domains and Motifs

Substances

  • Glutathione Transferase
  • Glutathione