detection-of-protease-activity-by-fluorescent-peptide-zymography

Detection of Protease Activity by Fluorescent Peptide Zymography

The purpose of this method is to measure the proteolytic activity of complex biological samples. The samples are separated by molecular weight using ...

Ohio State University

Current zymographic techniques detect only a subset of known proteases due to the limited number of native proteins that have been optimized for incorporation into polyacrylamide gels. To address this limitation, we have developed a technique to covalently incorporate fluorescently labeled, protease-sensitive peptides using an azido-PEG3-maleimide crosslinker. Peptides incorporated into gels enabled measurement of MMP-2, -9, -14, and bacterial collagenase. Sensitivity analysis demonstrated that use of peptide functionalized gels could surpass detection limits of current techniques. Finally, electrophoresis of conditioned media from cultured cells resulted in the appearance of several proteolytic bands, some of which were undetectable by gelatin zymography. Taken together, these results demonstrate that covalent incorporation of fluorescent substrates can greatly expand the library of detectable proteases using zymographic techniques.

Ameya A. Deshmukh

Comprehensive Cancer Center,
James Cancer Hospital and Solove Research Center,
Department of Biomedical Engineering,
College of Engineering,
Comprehensive Cancer Center, James Cancer Hospital and Solove Research Center,
Department of Biomedical Engineering, College of Engineering

Ohio State University

Detection of Protease Activity by Fluorescent Peptide Zymography