Abstract

Small molecule fluorescent probes provide a powerful labelling technology to enhance our understanding of particular proteins. However, the discovery of a proper fluorescent probe for detecting PDE5 is still a challenge due to the highly conservative structure of the catalytic domain in the phosphodiesterase (PDE) families. Herein, we identified probes based on the key amino residues in the ligand binding pocket of PDE5 and catalytic-site-fluorescent probes PCO2001–PCO2003 were well designed and synthesized. Among them, PCO2003 exhibited extraordinary fluorescence properties and the ability to be applied to PDE5 visualization in live cells as well as in pulmonary tissue slices, demonstrating the location and expression level of PDE5 proteins. Overall, the environment-sensitive “turn-on” probe is economical, convenient and rapid for PDE5 imaging, implying that the catalytic-site-fluorescent probe will have a variety of future applications in pathological diagnosis as well as drug screening.

Highlights

  • Information visible to the naked eye is always more convictive

  • Small molecule fluorescent probes provide a powerful labelling technology to enhance our understanding of particular proteins

  • PCO2003 exhibited extraordinary fluorescence properties and the ability to be applied to PDE5 visualization in live cells as well as in pulmonary tissue slices, demonstrating the location and expression level of PDE5 proteins

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Summary

Introduction

Information visible to the naked eye is always more convictive. It is usually impossible to obtain visual signals of most biomolecules, cells and organisms by direct observation. PCO2003 exhibited extraordinary fluorescence properties and the ability to be applied to PDE5 visualization in live cells as well as in pulmonary tissue slices, demonstrating the location and expression level of PDE5 proteins. All these probes could be predicted to have good electro-static interactions in allusion to amino acid residues of the catalytic pocket in PDE5 protein, contributing to the strong receptor-ligand binding patterns (Fig. S2, ESI†).

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