Viewing Individual Enzymes

  • ChemPubSoc Europe Logo
  • Author: Angewandte Chemie International Edition
  • Published Date: 25 August 2019
  • Source / Publisher: Angewandte Chemie International Edition/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: Viewing Individual Enzymes

Optical microscopy provides a non-invasive way to study living systems. The resolution of this technique, however, is limited by the diffraction of light. Single-molecule localization microscopy overcomes this limit by using probes that can be transformed between fluorescent and non-fluorescent forms. These simple on/off switches can be bound to proteins and enable the observation of these proteins based on their expression levels.


Zacharias Thiel and Pablo Rivera-Fuentes at ETH Zurich, Switzerland, developed a probe that enables the observation of single enzymes based on their activity. Nitroreductases, enzymes involved in the activation of cancer drugs, were used for this approach. The researchers designed a diazoindanone derivative of a rhodamine dye. This probe was activated sequentially by nitroreductases and light to generate a fluorophore. This fluorophore is crosslinked to the enzyme, which limits its diffusion and makes the imaging more precise.


Using this probe, the intracellular localization of active nitroreductases was mapped with single-molecule precision in a living cell. Such information could be essential for the development of improved therapies with fewer side effects.


 

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