The total protease activity in any given protein sample can be determined by subjecting it to a protease assay kit that uses a highly quenched dye-labelled protein substrate. Upon contact, the protease present in the sample will digest the substrate and release dye-labelled peptides in the process. Absorbance is then measured to determine protease activity. In general the more label released, the higher the signal will be.
The resulting absorbance values are then compared to a standard curve. In a nutshell, a standard curve is generated by allowing various known quantities of tyrosine to react with the reagent. To accurately measure the amount of tyrosine liberated in the process, you should create the standard curve by recording the absorbance values for the standards, the test samples and the blanks (for both standard and test samples) and calculate the difference between the absorbance of the test sample and the test blank. You can compute for the activity of enzyme in units per/ml by using the following equation: