QUANTITATIVE ZYMOGRAPHY - DETECTION OF PICOGRAM QUANTITIES OF GELATINASES

被引:785
作者
KLEINER, DE
STETLERSTEVENSON, WG
机构
[1] Laboratory of Pathology, National Cancer Institute, Bethesda
关键词
D O I
10.1006/abio.1994.1186
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Zymography is an electrophoretic technique used to identify proteolytic activity in enzymes separated in polyacrylamide gels under nonreducing conditions. It has been used extensively in the qualitative evaluation 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 gelatinase A, a matrix metalloprotease, is directly proportional to the amount 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 gelatinase activity as well as demonstrate its usefulness as a qualitative technique for the analysis of gelatinase species present. (C) 1994 Academic Press, Inc.
引用
收藏
页码:325 / 329
页数:5
相关论文
共 17 条
  • [1] MATRIX METALLOPROTEINASES - A REVIEW
    BIRKEDALHANSEN, H
    MOORE, WGI
    BODDEN, MK
    WINDSOR, LJ
    BIRKEDALHANSEN, B
    DECARLO, A
    ENGLER, JA
    [J]. CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) : 197 - 250
  • [2] BROWN PD, 1990, CANCER RES, V50, P6184
  • [3] ASSOCIATION BETWEEN EXPRESSION OF ACTIVATED 72-KILODALTON GELATINASE AND TUMOR SPREAD IN NON-SMALL-CELL LUNG-CARCINOMA
    BROWN, PD
    BLOXIDGE, RE
    STUART, NSA
    GATTER, KC
    CARMICHAEL, J
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (07) : 574 - 578
  • [4] EXPRESSION OF ACTIVATED GELATINASE IN HUMAN INVASIVE BREAST-CARCINOMA
    BROWN, PD
    BLOXIDGE, RE
    ANDERSON, E
    HOWELL, A
    [J]. CLINICAL & EXPERIMENTAL METASTASIS, 1993, 11 (02) : 183 - 189
  • [5] ACTIVITY OF TYPE-IV COLLAGENASES IN BENIGN AND MALIGNANT BREAST DISEASE
    DAVIES, B
    MILES, DW
    HAPPERFIELD, LC
    NAYLOR, MS
    BOBROW, LG
    RUBENS, RD
    BALKWILL, FR
    [J]. BRITISH JOURNAL OF CANCER, 1993, 67 (05) : 1126 - 1131
  • [6] STUDY OF PROTEASES AND PROTEASE-INHIBITOR COMPLEXES IN BIOLOGICAL-FLUIDS
    GRANELLIPIPERNO, A
    REICH, E
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (01) : 223 - 234
  • [7] ELECTROPHORETIC ANALYSIS OF PLASMINOGEN ACTIVATORS IN POLYACRYLAMIDE GELS CONTAINING SODIUM DODECYL-SULFATE AND COPOLYMERIZED SUBSTRATES
    HEUSSEN, C
    DOWDLE, EB
    [J]. ANALYTICAL BIOCHEMISTRY, 1980, 102 (01) : 196 - 202
  • [8] KATO Y, 1992, J BIOL CHEM, V267, P11424
  • [9] Structural biochemistry and activation of matrix metalloproteases
    Kleiner, David E., Jr.
    Stevenson, William G. Stetler
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (05) : 891 - 897
  • [10] HIGHER-ORDER COMPLEX-FORMATION BETWEEN THE 72-KILODALTON TYPE-IV COLLAGENASE AND TISSUE INHIBITOR OF METALLOPROTEINASES-2
    KLEINER, DE
    UNSWORTH, EJ
    KRUTZSCH, HC
    STETLERSTEVENSON, WG
    [J]. BIOCHEMISTRY, 1992, 31 (06) : 1665 - 1672