Gupta Priyadarshini, Rani Vibha
Transcriptome Laboratory, Centre of Emerging Diseases, Department of Biotechnology, Jaypee Institute of Information Technology, Noida, UP, India.
Methods Mol Biol. 2025;2917:213-223. doi: 10.1007/978-1-0716-4478-2_18.
Matrix metalloproteinases (MMPs) are proteolytic enzymes regulating the degradation of collagen as well as other proteins in the extracellular matrix (ECM), tissue repair, and remodeling. Validating MMPs as current drug targets can potentially establish the clinical relevance of their quantitative expression and distribution and open new therapeutic venues in tumor and metastasis. Zymography is a technique used for the identification of the proteolytic activity of MMPs in diverse biological samples. In gel diffusion zymography, analysis of the functional activity of the gelatinases (MMP-2 and MMP-9) by the digestion of gelatin as a substrate, added to agarose gel to assess the active forms of MMPs, is done. Here we describe a detailed experimental protocol to quantitate the gelatinase activity within the cell culture.
基质金属蛋白酶(MMPs)是一类蛋白水解酶,可调节细胞外基质(ECM)中胶原蛋白以及其他蛋白质的降解、组织修复和重塑。验证MMPs作为当前的药物靶点可能会确立其定量表达和分布的临床相关性,并为肿瘤和转移开辟新的治疗途径。酶谱法是一种用于鉴定多种生物样品中MMPs蛋白水解活性的技术。在凝胶扩散酶谱法中,通过将明胶作为底物进行消化来分析明胶酶(MMP-2和MMP-9)的功能活性,将其添加到琼脂糖凝胶中以评估MMPs的活性形式。在此,我们描述了一种详细的实验方案,用于定量细胞培养物中的明胶酶活性。