A real-time fluorescence assay for protease activity and inhibitor screening based on the aggregation-caused quenching of a perylene probe

Luminescence. 2018 Jun;33(4):790-796. doi: 10.1002/bio.3478. Epub 2018 Apr 1.

Abstract

We have established a real-time and label-free fluorescence turn-on strategy for protease activity detection and inhibitor screening via peptide-induced aggregation-caused quenching of a perylene probe. Because of electrostatic interactions and high hydrophilicity, poly-l-glutamic acid sodium salt (PGA; a negatively charged peptide) could induce aggregation of a positively charged perylene probe (probe 1) and the monomer fluorescence of probe 1 was effectively quenched. After a protease was added, PGA was enzymatically hydrolyzed into small fragments and probe 1 disaggregated. The fluorescence recovery of probe 1 was found to be proportional to the concentration of protease in the range from 0 to 1 mU/ml. The detection limit was down to 0.1 mU/ml. In the presence of a protease inhibitor, protease activity was inhibited and fluorescence recovery reduced. Moreover, we demonstrated the potential application of our method in a complex mixture sample including 1% human serum. Our method is simple, fast and cost effective.

Keywords: aggregation; fluorescence; peptide; perylene probe; protease activity.

MeSH terms

  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Fluorescent Dyes / chemistry
  • Fluorescent Dyes / pharmacology*
  • Peptides / chemistry
  • Perylene / chemistry
  • Perylene / pharmacology*
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / pharmacology*
  • Protein Aggregates / drug effects
  • Spectrometry, Fluorescence
  • Structure-Activity Relationship
  • Time Factors

Substances

  • Fluorescent Dyes
  • Peptides
  • Protease Inhibitors
  • Protein Aggregates
  • Perylene