A novel simple fluorometric protease assay for monitoring hydrolysis of proteins in real time

Measuring the activity of proteases is essential for investigating both the physiological functions and commercial applications of these enzymes. In contrast to the numerous protease assays that are based on chromogenic or fluorogenic peptide substrates, there is a lack of approaches to monitor degradation of proteins in real time. Here we report a protease assay where SYPRO Orange is employed as a fluorogenic probe to follow proteolysis. The functionality of the assay was demonstrated with the two subtilases of varying thermostability, using four different protein substrates. The assay is compatible with a real-time PCR instrument which allows continuous fluorescence measurements in low-volume samples even at high temperatures. This makes the assay especially suitable for high-throughput characterization of thermostable proteases.

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Publication Details

Journal
Analytical Biochemistry
Published
2024-10-16
DOI
https://doi.org/10.1016/j.ab.2024.115688
Citations
1
Primary Topic
Protein purification and stability
Type
article
Field-Weighted Citation Impact
0.23

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article

A novel simple fluorometric protease assay for monitoring hydrolysis of proteins in real time

Miha Bahun, Nataša Poklar Ulrih
1 citations
Analytical Biochemistry
Protein purification and stability
0.23
article

A novel simple fluorometric protease assay for monitoring hydrolysis of proteins in real time

Miha Bahun, Nataša Poklar Ulrih
article en
1 citations

Abstract

Measuring the activity of proteases is essential for investigating both the physiological functions and commercial applications of these enzymes. In contrast to the numerous protease assays that are based on chromogenic or fluorogenic peptide substrates, there is a lack of approaches to monitor degradation of proteins in real time. Here we report a protease assay where SYPRO Orange is employed as a fluorogenic probe to follow proteolysis. The functionality of the assay was demonstrated with the two subtilases of varying thermostability, using four different protein substrates. The assay is compatible with a real-time PCR instrument which allows continuous fluorescence measurements in low-volume samples even at high temperatures. This makes the assay especially suitable for high-throughput characterization of thermostable proteases.

Analytical BiochemistryVol. 696
University of Ljubljana (SI), Centre of Excellence for Integrated Approaches in Chemistry and Biology of Proteins (SI)
Javna Agencija za Raziskovalno Dejavnost RS
Openalex Percentile: Top 42%
Protein purification and stability
0.23
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