A homo-FRET assay for patatin-specific proteolytic activity
The potato protein patatin embeds bioactive peptides that require targeted hydrolysis to be released as promising food additives. This study presents a patatin-specific protease assay for assessing a wide range of protease activities in high-throughput format. Conjugating patatin to the amine reactive fluorogenic BODIPY FL dye provided a stable protease substrate with efficient homo-FRET quenching at a low degree (7-8) of labeling. Compared to commercial BODIPY-casein, BODIPY-patatin provided higher fluorescence enhancement (by de-quenching) at high protease concentrations, while the sensitivity was generally comparable for both highly specific (e.g. Trypsin) and industrial relevant proteases (e.g. Alcalase and Neutrase) at low doses. For Chymotrypsin, BODIPY-patatin provided a 39 % response improvement at 5 ng dose. A peptide-centric analysis of mass spectrometry-based bottom-up proteomics data identified several BODIPY-labeling sites with varying occupancies in patatin, indicating heterogenous labeling under the applied conjugation conditions. BODIPY-labeled patatin complements commercial BODIPY-labeled casein as a globular, plant-based alternative for screening of proteolytic activity.
Authors
- Michael T. Overgaard (ORCID: https://orcid.org/0000-0002-1423-2481)
- Egon Bech Hansen (ORCID: https://orcid.org/0000-0002-3795-6706)
- Lise Friis Christensen (ORCID: https://orcid.org/0000-0002-4103-2768)
- Simon Gregersen Echers (ORCID: https://orcid.org/0000-0001-9349-3235)
Institutions
- Aalborg University (DK)
- Technical University of Denmark (DK)
Publication Details
- Journal
- Food Chemistry
- Published
- 2024-09-02
- DOI
- https://doi.org/10.1016/j.foodchem.2024.141105
- Citations
- 2
- Primary Topic
- Protein Hydrolysis and Bioactive Peptides
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- Innovationsfonden