BODIPY-alpha-casein, a pH-independent protein substrate for protease assays using fluorescence polarization

被引:41
作者
Schade, SZ [1 ]
Jolley, ME [1 ]
Sarauer, BJ [1 ]
Simonson, LG [1 ]
机构
[1] JOLLEY CONSULTING & RES INC,GRAYSLAKE,IL 60030
关键词
D O I
10.1006/abio.1996.0475
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
BODIPY-alpha-casein is a new fluorescent protein substrate designed for fluorescence polarization studies to measure proteolytic activity at any pH over the range from pH 2 to 11. Kinetic protease assays in real-time were performed in 1 to 5 min using an FPM-1 fluorescence polarization instrument. A purified enzyme or bacterial culture was mixed with the BODIPY-alpha-casein in a buffer of an appropriate pH and the decrease in fluorescence polarization was automatically recorded at 0.5-min intervals. The initial decrease in fluorescence polarization with time was dependent on protease concentration. In 3-min assays at 37 degrees C, the sensitivity of detection was 8 mU for pepsin at pH 2.0, 1 mU for papain at pH 6.0, 0.6 mU for proteinase It at pH 1.4, and 2 mU for Streptomyces griseus alkaline protease at pH 11. Only 1-10 mu l of a growing culture was necessary to assay the protease activity of Porphyromonas gingivalis or Treponema denticola, oral bacteria that possess certain proteases on their surfaces. These assays have clinical applications, since certain pathogens use proteolytic activity as a virulence mechanism and differ hom their nonpathogenic counterparts in this characteristic. Fluorescence polarization assays are simple, rapid, and reproducible. (C) 1996 Academic Press Inc.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 15 条
[1]  
BOLGER R, 1994, BIOTECHNIQUES, V17, P585
[2]   QUANTIFICATION OF ANTIGEN-ANTIBODY REACTION BY POLARIZATION OF FLUORESCENCE [J].
DANDLIKER, W ;
FEIGEN, GA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1961, 5 (04) :299-&
[3]   EVALUATION OF SERUM-CONTAINING SUBSTRATES FOR CULTIVATION OF ORAL SPIROCHETES [J].
FIEHN, NE ;
FRANDSEN, A .
JOURNAL OF PERIODONTAL RESEARCH, 1984, 19 (01) :61-66
[4]   CELLULAR LOCATION OF A TREPONEMA-DENTICOLA CHYMOTRYPSINLIKE PROTEASE AND IMPORTANCE OF THE PROTEASE IN MIGRATION THROUGH THE BASEMENT-MEMBRANE [J].
GRENIER, D ;
UITTO, VJ ;
MCBRIDE, BC .
INFECTION AND IMMUNITY, 1990, 58 (02) :347-351
[6]   ASSAY OF PROTEOLYTIC-ENZYMES BY THE FLUORESCENCE POLARIZATION TECHNIQUE [J].
MAEDA, H .
ANALYTICAL BIOCHEMISTRY, 1979, 92 (01) :222-227
[7]   THE MULTIPLE FORMS OF TRYPSIN-LIKE ACTIVITY PRESENT IN VARIOUS STRAINS OF PORPHYROMONAS-GINGIVALIS ARE DUE TO THE PRESENCE OF EITHER ARG-GINGIPAIN OR LYS-GINGIPAIN [J].
POTEMPA, J ;
PIKE, R ;
TRAVIS, J .
INFECTION AND IMMUNITY, 1995, 63 (04) :1176-1182
[8]   PROTEASES OF TREPONEMA-DENTICOLA OUTER SHEATH AND EXTRACELLULAR VESICLES [J].
ROSEN, G ;
NAOR, R ;
RAHAMIM, E ;
YISHAI, R ;
SELA, MN .
INFECTION AND IMMUNITY, 1995, 63 (10) :3973-3979
[9]   PRODUCTION AND CHARACTERIZATION OF MONOCLONAL-ANTIBODIES TO BACTEROIDES-GINGIVALIS [J].
SIMONSON, LG ;
MERRELL, BR ;
ROUSE, RF ;
SHKLAIR, IL .
JOURNAL OF DENTAL RESEARCH, 1986, 65 (02) :95-97
[10]   EFFECT OF SALTS UPON PH-DEPENDENCE OF ACTIVITY OF PAPAIN AND SUCCINYL-PAPAIN [J].
SLUYTERM.LA ;
DEGRAAF, MJM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 258 (02) :554-&