Off-On Squalene Epoxidase-Specific Fluorescent Probe for Fast Imaging in Living Cells.

Anal Chem

Key Laboratory of Cluster Science of Ministry of Education, Beijing Key Laboratory of Photo-electronic/Electro-photonic Conversion Materials, Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, Analytical and Testing Center, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, People's Republic of China.

Published: November 2021

AI Article Synopsis

  • SQLE is an enzyme that is a focus for new cancer therapies and fungicides, but tracking it in live cells is tough.
  • A new fluorescent probe called TPE-Ter has been developed that can bind specifically to SQLE, showing strong emission signals and quick responses.
  • Tests in live cells and fungi show that TPE-Ter can effectively monitor SQLE levels and help assess antifungal drug effectiveness in just about 30 minutes.

Article Abstract

SQLE (squalene epoxidase) is a cell membrane-bound enzyme. It is a target of fungicides and may become a new target for cancer therapy. Therefore, monitoring the content and distribution of the key enzyme in living cells is very challenging. To achieve this goal, tetraphenyl ethylene-Ter (TPE-Ter) was first designed as a new fluorescent probe to SQLE based on its active cavity. Spectral experiments discovered that SQLE/TPE-Ter shows stronger emission with fast response time and low interference from other analytes. Molecular dynamics simulation clearly confirmed the complex structure of SQLE/TPE-Ter, and the key residues contribute to restriction of TPE-Ter single-molecular motion in the cavity. TPE-Ter-specific response to SQLE is successfully demonstrated in living cells such as LO2, HepG2, and fungi. Imaging of TPE-Ter-treated fungi indicates that it can be used to rapidly assess antifungal drug susceptibility (30 min at least). The present work provides a powerful tool to detect content and distribution of SQLE in living cells.

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http://dx.doi.org/10.1021/acs.analchem.1c03168DOI Listing

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