Quenched BODIPY Dye-Labeled Casein Substrates for the Assay of Protease Activity by Direct Fluorescence Measurement

• Published in: Analytical biochemistry Vol. 251; no. 2; pp. 144 - 152
• Main Authors: Jones, Laurie J., Upson, Rosalyn H., Haugland, Rosaria P., Panchuk-Voloshina, Nataliya, Zhou, Mingjie, Haugland, Richard P.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 05-09-1997
• Subjects: Animals; Boron Compounds; Caseins - chemistry; Endopeptidases - analysis; Fluorescein-5-isothiocyanate; Fluorescent Antibody Technique, Direct; Fluorescent Dyes; Humans; Hydrolysis; Protease Inhibitors - analysis; Spectrometry, Fluorescence; Xanthenes
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1006/abio.1997.2259

We have prepared casein conjugates of two BODIPY dyes for use as fluorogenic protease substrates in homogeneous assays. Both conjugates are labeled to such an extent that the dyes are efficiently quenched in the protein, yielding virtually nonfluorescent substrate molecules. These fluorogenic substrates release highly fluorescent BODIPY dye-labeled peptides upon protease digestion, with fluorescence increases proportional to enzyme activity. These quenched substrates are suitable for the continuous assay of enzymatic activity using standard fluorometers, filter fluorometers, or fluorescence microplate readers using either fluorescein excitation and emission wavelengths to measure BODIPY FL casein hydrolysis or Texas Red wavelengths to detect proteolysis of BODIPY TR-X casein. Most current techniques for detecting protease activity, such as the fluorescein thiocarbamoyl casein (FTC–casein) protease assay, require extensive manipulation, including separation steps, and are therefore labor intensive and error-prone. In comparison, we found the BODIPY dye-labeled casein protease assays to be simple and precise and to have greater sensitivity and a broader dynamic range of detection than the FTC-casein assay. We were able to sensitively detect the activities of a wide variety of enzymes with these new substrates, including serine, acid, sulfhydryl, and metalloproteases. We also found the assay suitable for quantitating protease inhibitor concentrations and for real-time analysis of proteolysis.