Assessment of gelatinases (MMP-2 and MMP-9) by gelatin zymography.

Methods Mol Biol

Department of Pathology, School of Medicine, Proteases and Cancer Program, Karmanos Cancer Institute, Wayne State University, Detroit, MI, USA.

Published: October 2012

AI Article Synopsis

  • Gelatin zymography is an effective technique for detecting proteolytic enzymes that degrade gelatin, especially MMP-2 and MMP-9, which are important in various biological processes.
  • This method utilizes polyacrylamide gel electrophoresis to assess the type, amount, and activation status of gelatinases in samples from cells, tissues, and biological fluids.
  • Proper interpretation of the data is crucial to avoid pitfalls, making it a valuable tool for studying gelatinase expression and its implications in cancer progression.

Article Abstract

Gelatin zymography is a simple yet powerful method to detect proteolytic enzymes capable of degrading gelatin from various biological sources. It is particularly useful for the assessment of two key members of the matrix metalloproteinase family, MMP-2 (gelatinase A) and MMP-9 (gelatinase B), due to their potent gelatin-degrading activity. This polyacrylamide gel electrophoresis-based method can provide a reliable assessment of the type of gelatinase, relative amount, and activation status (latent, compared with active enzyme forms) in cultured cells, tissues, and biological fluids. The method can be used to investigate factors that regulate gelatinase expression and modulate zymogen activation in experimental systems. The system provides information on the pattern of gelatinase expression and activation in human cancer tissues and how this relates to cancer progression. Interpretation of the data obtained in gelatin zymography requires a thorough understanding of the principles and pitfalls of the technique; this is particularly important when evaluating enzyme levels and the presence of active gelatinase species. If properly used, gelatin zymography is an excellent tool for the study of gelatinases in biological systems.

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http://dx.doi.org/10.1007/978-1-61779-854-2_8DOI Listing

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