Detection of femtomole quantities of mature cathepsin K with zymography

Cathepsin K, the most potent mammalian collagenase, has been implicated in osteoporosis, Cancer metastasis, atherosclerosis, and arthritis. Although procathepsin K is stable and readily detected, the active mature Cathepsin K eludes detection by in vitro methods due to its shorter half-life and inactivation at neutral pH. We describe, for the first time, reliable detection, visualization, and quantification of mature Cathepsin K to femtomole resolution using gelatin zymography. The specificity of the method was validated with Cathepsin K knockdown using small interfering RNA (siRNA) transfection of human monocyte-derived macrophages, and enzymatic activity confirmed with benzyloxycarbonyl-glycine-proline-arginine-7-amino-4-methylcoumarin (Z-GPR-AMC) substrate hydrolysis was fit to a computational model of Enzyme kinetics. Furthermore, Cathepsin K zymography was used to show that murine osteoclasts secrete more Cathepsin K than is stored intracellularly, and this was opposite to the behavior of the macrophages from which they were differentiated. In summary, this inexpensive, species-independent, antibody-free protocol describes a sensitive method with broad potential to elucidate previously undetectable Cathepsin K activity.