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黑色素瘤中利用胶原蛋白酶谱分析法分析基质金属蛋白酶(MMP)的酶活性

Analysis of Enzymatic Activity of Matrix Metalloproteinase (MMP) by Collagen Zymography in Melanoma.

作者信息

Walia Vijay, Samuels Yardena

机构信息

Laboratory of Cell and Developmental Signaling, National Cancer Institute-Frederick, Frederick, MD, USA.

Molecular Cell Biology Department, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Methods Mol Biol. 2018;1731:97-106. doi: 10.1007/978-1-4939-7595-2_10.

Abstract

Protein zymography is the most commonly used technique to study the enzymatic activity of matrix metalloproteinases (MMPs) and their inhibitors. MMPs are proteolytic enzymes that promote extracellular matrix degradation. MMPs are frequently mutated in malignant melanomas as well as other cancers and are linked to increasing incidence of tumor metastasis. Substrate zymography characterizes MMP activity by their ability to degrade preferred substrates. Here we describe the collagen zymography technique to measure the active or latent form of MMPs using MMP-8 as an example, which is a frequently mutated MMP family member in malignant melanomas. The same technique can be used with the modification of substrate to detect metalloproteinase activity of other MMPs. Both wild-type and mutated forms of MMPs can be analyzed using a single gel using this method.

摘要

蛋白质酶谱法是研究基质金属蛋白酶(MMPs)及其抑制剂酶活性最常用的技术。MMPs是促进细胞外基质降解的蛋白水解酶。MMPs在恶性黑色素瘤以及其他癌症中经常发生突变,并与肿瘤转移发生率增加有关。底物酶谱法通过MMPs降解首选底物的能力来表征其活性。在这里,我们以MMP-8为例描述胶原蛋白酶谱技术,以测量MMPs的活性或潜伏形式,MMP-8是恶性黑色素瘤中经常发生突变的MMP家族成员。通过对底物进行修饰,相同的技术可用于检测其他MMPs的金属蛋白酶活性。使用该方法可以在一块凝胶上分析MMPs的野生型和突变型。

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