De. Kleiner et Wg. Stetlerstevenson, QUANTITATIVE ZYMOGRAPHY - DETECTION OF PICOGRAM QUANTITIES OF GELATINASES, Analytical biochemistry, 218(2), 1994, pp. 325-329
Zymography is an electrophoretic technique used to identify proteolyti
c activity in enzymes separated in polyacrylamide gels under nonreduci
ng conditions. It has been used extensively in the qualitative evaluat
ion of proteases present in tumors and cell culture conditioned media.
Using commercially available precast gels and a modern image analysis
system, we have evaluated zymography as a quantitative technique. The
degree of digestion of gelatin within the zymogram by purified gelati
nase A, a matrix metalloprotease, is directly proportional to the amou
nt of enzyme loaded over a 10- 20-fold range. With an overnight (18 h)
digestion period, the linear range of this assay extended from 10 to
120 pg of enzyme. The initial rate of digestion is proportional to the
enzyme loading and varying the incubation time results in a shift in
the linear range of the assay. Active and latent forms of gelatinase A
show the same degree of digestion in this assay system. These results
justify the use of zymography in the quantitative assessment of gelat
inase activity as well as demonstrate its usefulness as a qualitative
technique for the analysis of gelatinase species present. (C) 1994 Aca
demic Press, Inc.