George Joseph
Department of Hepatology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Methods Mol Biol. 2025;2918:187-199. doi: 10.1007/978-1-0716-4482-9_15.
Zymography is an electrophoretic technique to measure the proteolytic activity of native enzymes on a nonreducing sodium dodecyl sulfate polyacrylamide gel. It is a simple and powerful tool to assess the amount of various proteases present in both physiological and pathological conditions. The concerned protease degrades the protein substrate that is incorporated with the gel and resolves during the incubation period. Staining with Coomassie brilliant blue (CBB) reveals the sites of proteolysis as clear white bands. The intensity and area of the bands are linearly related to the amount of protease present in the loaded sample. Matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9), also known as gelatinases, have the indigenous property to digest gelatin and several other protein molecules present in the extracellular matrix. Here, we describe the detailed protocols and methods of zymography, with a special emphasis on the determination of gelatinases present in conditioned culture media and tissue extracts.
酶谱法是一种电泳技术,用于在非还原十二烷基硫酸钠聚丙烯酰胺凝胶上测量天然酶的蛋白水解活性。它是评估生理和病理条件下各种蛋白酶含量的一种简单而强大的工具。相关蛋白酶会降解与凝胶结合并在孵育期分解的蛋白质底物。用考马斯亮蓝(CBB)染色会将蛋白水解位点显示为清晰的白色条带。条带的强度和面积与上样样品中蛋白酶的含量呈线性相关。基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶-9(MMP-9),也称为明胶酶,具有消化明胶和细胞外基质中存在的其他几种蛋白质分子的固有特性。在此,我们描述酶谱法的详细方案和方法,特别强调对条件培养基和组织提取物中明胶酶的测定。