Novel immuno-FRET assay method for Bacillus spores and Escherichia coli O157:H7

被引:12
作者
Bruno, JG
Ulvick, SJ
Uzzell, GL
Tabb, JS
Valdes, ER
Batt, CA
机构
[1] OmniSite Biodiagnost Inc, Austin, TX 78701 USA
[2] Agave Biosyst Inc, Ithaca, NY 14851 USA
[3] USA, ECBC, Aberdeen Proving Ground, MD 21010 USA
[4] Cornell Univ, Alliance Nanomed Technol, Ithaca, NY 14853 USA
关键词
bacteria; Bacillus; fluorescence; E. coli O157 : H7; FRET; immunofluorescence; Oregon Green; QSY-7; quencher; spores;
D O I
10.1006/bbrc.2001.5669
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Novel immunofluorescence resonance energy transfer (immuno-FRET) assays for both Bacillus cereus spores and Escherichia coli O157:H7 are reported. Both assays involve the use of dual (QSY-7 and Oregon Green 514-antibody)-labeled spores or vegetative bacteria, such that Oregon Green 514-labeled antibodies are quenched by proximal QSY-7 molecules that are covalently bound to the dual (Oregon Green 514 and QSY-7)-labeled cells. Upon introduction of unlabeled bacteria or spores, in the respective assays, an increase in fluorescence is observed in proportion to the numbers of unlabeled cells. This is due to migration of Oregon Green 514-labeled antibody from the dual-labeled cells to the unlabeled target cells as verified by fluorescence microscopy. Optimization of the QSY-7 surface density led to a B. cereus spore detection sensitivity of approximately 1.0 x 10(5) to 2.5 x 10(5) spores per milliliter and 3.5 x 10(5) cells per milliliter for E. coli using a conventional cuvette-based spectrofluorometer. (C) 2001 Academic Press.
引用
收藏
页码:875 / 880
页数:6
相关论文
共 15 条
[1]  
[Anonymous], NUCL ACIDS RES
[2]   Quantitative fluorescence resonance energy transfer measurements using fluorescence microscopy [J].
Gordon, GW ;
Berry, G ;
Liang, XH ;
Levine, B ;
Herman, B .
BIOPHYSICAL JOURNAL, 1998, 74 (05) :2702-2713
[3]   In vitro selection of signaling aptamers [J].
Jhaveri, S ;
Rajendran, M ;
Ellington, AD .
NATURE BIOTECHNOLOGY, 2000, 18 (12) :1293-1297
[4]   Development of a fluorogenic probe-based PCR assay for detection of Bacillus cereus in nonfat dry milk [J].
Kim, YR ;
Czajka, J ;
Batt, CA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (04) :1453-1459
[5]   FLUORESCENCE RESONANCE ENERGY-TRANSFER AS A NEW METHOD FOR THE EPITOPE-SPECIFIC CHARACTERIZATION OF ANTIPLATETLET ANTIBODIES [J].
KOKSCH, M ;
ROTHE, G ;
KIEFEL, V ;
SCHMITZ, G .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 187 (01) :53-67
[6]  
Koo K, 1998, APPL ENVIRON MICROB, V64, P2497
[7]  
Koo K, 1998, APPL ENVIRON MICROB, V64, P2490
[8]  
LIVAK KJ, 1995, PCR METH APPL, V4, P357
[9]   Fluorescence resonance energy transfer from pyrene to perylene labels for nucleic acid hybridization assays under homogeneous solution conditions [J].
Masuko, Masayuki ;
Ohuchi, Shohkichi ;
Sode, Koji ;
Ohtani, Hiroyuki ;
Shimadzu, Akira .
NUCLEIC ACIDS RESEARCH, 2000, 28 (08) :34
[10]   Molecular mechanisms of peptide loading by the tumor rejection antigen heat shock chaperone gp96 (GRP94) [J].
Sastry, S ;
Linderoth, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :12023-12035