Zhang Yue, Wan Rong, Zhang Qunwei, Mo Yiqun
Department of Environmental and Occupational Health Sciences, School of Public Health and Information Sciences, University of Louisville, Louisville, KY, USA.
Methods Mol Biol. 2019;1894:133-143. doi: 10.1007/978-1-4939-8916-4_8.
Gelatin zymography is a relatively simple, inexpensive, and powerful technique to detect proteolytic enzymes capable of degrading gelatin from various biological sources. It has been used particularly to detect the two members of the matrix metalloproteinase family, MMP-2 (gelatinase A) and MMP-9 (gelatinase B), due to their potent gelatin-degrading activity. MMP-2 and MMP-9 are also able to degrade a number of extracellular matrix molecules including type IV, V, and XI collagens, laminin, and aggrecan core protein, thus making them important in the nanotoxicity research. In this technique, proteins are separated by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE), and gelatinases, activated by SDS, digest gelatin embedded in the gel. After staining with Coomassie Brilliant Blue R-250, areas of degradation are visible as clear bands against a blue-stained background. Here, we describe the detailed procedure for gelatin zymography.
明胶酶谱法是一种相对简单、成本低廉且功能强大的技术,用于检测能够降解来自各种生物来源的明胶的蛋白水解酶。由于基质金属蛋白酶家族的两个成员MMP - 2(明胶酶A)和MMP - 9(明胶酶B)具有强大的明胶降解活性,该技术尤其用于检测它们。MMP - 2和MMP - 9还能够降解多种细胞外基质分子,包括IV型、V型和XI型胶原蛋白、层粘连蛋白和聚集蛋白聚糖核心蛋白,因此它们在纳米毒性研究中具有重要意义。在这项技术中,蛋白质通过十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳(PAGE)进行分离,被SDS激活的明胶酶会消化凝胶中包埋的明胶。用考马斯亮蓝R - 250染色后,降解区域在蓝色背景下呈现为清晰的条带。在此,我们描述明胶酶谱法的详细步骤。