Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA 30332, USA.
Anal Biochem. 2010 Jun 1;401(1):91-8. doi: 10.1016/j.ab.2010.02.035. Epub 2010 Mar 3.
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.
组织蛋白酶 K 是最有效的哺乳动物胶原酶,与骨质疏松症、癌症转移、动脉粥样硬化和关节炎有关。虽然原组织蛋白酶 K 稳定且易于检测,但由于其半衰期较短且在中性 pH 下失活,活性成熟的组织蛋白酶 K 难以通过体外方法检测。我们首次描述了使用明胶酶谱法可靠地检测、可视化和定量纳摩尔分辨率的成熟组织蛋白酶 K。该方法的特异性通过用小干扰 RNA (siRNA) 转染人单核细胞来源的巨噬细胞来降低组织蛋白酶 K 进行了验证,并且用苯甲氧基羰基-甘氨酸-脯氨酸-精氨酸-7-氨基-4-甲基香豆素 (Z-GPR-AMC) 底物水解的酶活性进行拟合来验证酶动力学的计算模型。此外,组织蛋白酶 K 酶谱法用于表明,与分化而来的巨噬细胞相反,破骨细胞分泌的组织蛋白酶 K 多于细胞内储存的组织蛋白酶 K。总之,这种廉价、与物种无关且无需抗体的方案描述了一种灵敏的方法,具有阐明以前无法检测到的组织蛋白酶 K 活性的广泛潜力。