Matrix metalloproteinase activity assays: Importance of zymography

被引:119
作者
Kupai, K. [1 ]
Szucs, G. [1 ]
Cseh, S. [2 ]
Hajdu, I. [2 ]
Csonka, C. [1 ,3 ]
Csont, T. [1 ,3 ]
Ferdinandy, P. [1 ,3 ]
机构
[1] Univ Szeged, Cardiovasc Res Grp, Dept Biochem, H-6720 Szeged, Hungary
[2] TargetEx, Dunakeszi, Hungary
[3] Pharmahungary Grp, Szeged, Hungary
关键词
Matrix metalloproteinases; MMP inhibitors; FRET; Zymography; IN-SITU ZYMOGRAPHY; BREAST-CANCER; METALLOELASTASE MMP-12; RHEUMATOID-ARTHRITIS; EXPRESSION; INHIBITORS; ATHEROSCLEROSIS; STIMULATION; COLLAGENASE; MT5-MMP;
D O I
10.1016/j.vascn.2010.02.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases capable of degrading extracellular matrix, including the basement membrane. MMPs are associated with various physiological processes such as morphogenesis, angiogenesis, and tissue repair. Moreover, due to the novel non-matrix related intra- and extracellular targets of MMPs, dysregulation of MMP activity has been implicated in a number of acute and chronic pathological processes, such as arthritis, acute myocardial infarction, chronic heart failure, chronic obstructive pulmonary disease, inflammation, and cancer metastasis. MMPs are considered as viable drug targets in the therapy of the above diseases. Methods: For the development of selective MMP inhibitor molecules, reliable methods are necessary for target validation and lead development. Here, we discuss the major methods used for MMP assays, focusing on substrate zymography. We highlight some problems frequently encountered during sample preparations, electrophoresis, and data analysis of zymograms. Results and Discussion: Zymography is a widely used technique to study extracellular matrix-degrading enzymes, such as MMPs, from tissue extracts, cell cultures, serum or urine. This simple and sensitive technique identifies MMPs by the degradation of their substrate and by their molecular weight and therefore helps to understand the widespread role of MMPs in different pathologies and cellular pathways. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:205 / 209
页数:5
相关论文
共 48 条
[1]   Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancer [J].
Ahokas, K ;
Lohi, J ;
Lohi, H ;
Elomaa, O ;
Karjalainen-Lindsberg, ML ;
Kere, J ;
Saarialho-Kere, U .
GENE, 2002, 301 (1-2) :31-41
[2]   Conformational variability of matrix metalloproteinases: Beyond a single 3D structure [J].
Bertini, I ;
Calderone, V ;
Cosenza, M ;
Fragai, M ;
Lee, YM ;
Luchinat, C ;
Mangani, S ;
Terni, B ;
Turano, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (15) :5334-5339
[3]   Tissue inhibitors of metalloproteinases: evolution, structure and function [J].
Brew, K ;
Dinakarpandian, D ;
Nagase, H .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1477 (1-2) :267-283
[4]   Understanding the role of tissue degrading enzymes and their inhibitors in development and disease [J].
Cawston, Tim E. ;
Wilson, Amy J. .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2006, 20 (05) :983-1002
[5]   Molecular balance of capillary tube formation versus regression in wound repair: Role of matrix metalloproteinases and their inhibitors [J].
Davis, George E. ;
Saunders, W. Brian .
JOURNAL OF INVESTIGATIVE DERMATOLOGY SYMPOSIUM PROCEEDINGS, 2006, 11 (01) :44-56
[6]   Development of selective inhibitors and substrate of matrix metalloproteinase-12 [J].
Devel, L ;
Rogakos, V ;
David, A ;
Makaritis, A ;
Beau, F ;
Cuniasse, P ;
Yiotakis, A ;
Dive, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (16) :11152-11160
[7]  
Dorman Gyorgy, 2007, Recent Pat Cardiovasc Drug Discov, V2, P186, DOI 10.2174/157489007782418964
[8]   MMP7 expression regulated by endocrine therapy in ERβ-positive colon cancer cells [J].
Fang, Yu-Jing ;
Pan, Zhi-Zhong ;
Li, Li-Ren ;
Lu, Zhen-Hai ;
Zhang, Li-Yi ;
Wan, De-Sen .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2009, 28
[9]   ENHANCED DETECTION OF CASEIN ZYMOGRAPHY OF MATRIX METALLOPROTEINASES [J].
FERNANDEZRESA, P ;
MIRA, E ;
QUESADA, AR .
ANALYTICAL BIOCHEMISTRY, 1995, 224 (01) :434-435
[10]   Metalloproteinase MT5-MMP is an essential modulator of neuro-immune interactions in thermal pain stimulation [J].
Folgueras, Alicia R. ;
Valdes-Sanchez, Teresa ;
Llano, Elena ;
Menendez, Luis ;
Baamonde, Ana ;
Denlinger, Bristol L. ;
Belmonte, Carlos ;
Juarez, Lucia ;
Lastra, Ana ;
Garcia-Suarez, Olivia ;
Astudillo, Aurora ;
Kirstein, Martina ;
Pendas, Alberto M. ;
Farinas, Isabel ;
Lopez-Otin, Carlos .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (38) :16451-16456