Zymography is an electrophoretic technique, based on
SDS-PAGE, that includes a substratecopolymerized with the polyacrylamidegel, for the detection of enzymeactivity. [cite journal |author= Lantz MS, Ciborowski P|title=Zymographic techniques for detection and characterization of microbial proteases. |journal= Methods Enzymol.|volume=235 |pages=563-594|year=1994|pmid=8057927] Samples are prepared in the standard SDS-PAGEtreatment buffer but without boiling, and without a reducing agent. Following electrophoresis, the SDS is removed from the gel (or zymogram) by incubation in unbuffered Triton X-100, followed by incubation in an appropriate digestion buffer, for an optimized length of time at 37°C. The zymogram is subsequently stained (commonly with Amido Black or Coomassie Brilliant Blue), and areas of digestion appear as clear bands against a darkly stained background where the substrate has been degraded by the enzyme. These protocols, however, are subject to much adjustment. For instance, "D. melanogaster" digestive glycosidases generally survive reducing conditions (i.e. the presence of 2-mercaptoethanol or DTT) and to an extent heating. Indeed, the separations following heating to 50 deg. C tend to exhibit a substantial increase in band resolution, without appreciable loss of activity. [cite journal |author= Martínez TF, Alarcón FJ, Díaz-López M, Moyano FJ|title= Improved detection of amylase activity by sodium dodecyl sulfate-polyacrylamide gel electrophoresis with copolymerized starch.|journal= Electrophoresis|volume= 21|pages=2940-2943|year=2000|pmid=11001307] [cite journal |author= Snoek-van Beurden PA, Von den Hoff JW|title= Zymographic techniques for the analysis of matrix metalloproteinases and their inhibitors.|journal= Biotechniques|volume=38 |pages=73-83|year=2005|pmid=15679089 ]
Gelatin is the most commonly used substrate, and is useful for demonstrating the activity of gelatin-degrading proteases, but zymography has been applied to a variety of enzymes, including xylanases, proteases, lipases, chitinases, etc.
A common protocol used in the past for zymography of α-amylase activity was the so-called starch film protocol of W.W. Doane. Here a native PAGE gel was run to separate the proteins in a homogenate. Subsequently, a thin gel with starch dissolved (or more properly, suspended) in it was overlaid for a period of time on top of the original gel. The starch was then stained with Lugol's iodine. Reverse zymography copolymerizes both the substrate and the enzyme with the acrylamide, and is useful for the demonstration of enzyme inhibitor activity. Following staining, areas of inhibition are visualized as dark bands against a clear (or lightly stained) background.
Imprint technique the enzyme is separated by native gel electrophoresis and the gel is laid on top of a substrate treated agarose.
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zymography — noun A form of electrophoresis used in the study of enzyme activity … Wiktionary
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zymographic — adjective Of or pertaining to zymography … Wiktionary