Fluorescence polarization immunoassay:: Detection of antibody to Brucella abortus

被引:42
作者
Nielsen, K
Lin, M
Gall, D
Jolley, M
机构
[1] Canadian Food Inspect Agcy, Anim Dis Res Inst, Nepean, ON K2H 8P9, Canada
[2] Jolley Consulting & Res Inc, Grayslake, IL 60030 USA
来源
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY | 2000年 / 22卷 / 01期
关键词
D O I
10.1006/meth.2000.1038
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence polarization immunoassay (FPA) is a homogeneous immunoassay useful for rapid and accurate detection of antibody or antigen. The principle of the assay is that a fluorescent dye (attached to an antigen or an antibody fragment) can be excited by plane-polarized light at the appropriate wavelength. As a rule, a small molecule rotates faster when in solution than a larger molecule, The rotation rate may be assessed by measuring light intensity in the vertical and horizontal planes. Generally, the time it takes a molecule to rotate through a given angle is an indication of its size. When a small molecule that rotates rapidly is bound to a larger molecule, the rotation rate is decreased and this decrease is measured. Because it Is a primary antigen-antibody interaction, the rate of reaction is very rapid and usually a result may be obtained in minutes. This technology was applied to the detection of antibody to Brucella abortus in serum and milk, providing for the first time a rapid primary binding assay that is cost effective for use in the field. (C) 2000 Academic Press.
引用
收藏
页码:71 / 76
页数:6
相关论文
共 22 条
[1]  
BENTLEY K L, 1985, Biotechniques, V3, P356
[2]  
BOLGER R, 1994, BIOTECHNIQUES, V17, P585
[3]  
Bolger R, 1994, Am Biotechnol Lab, V12, P116
[4]   QUANTIFICATION OF ANTIGEN-ANTIBODY REACTION BY POLARIZATION OF FLUORESCENCE [J].
DANDLIKER, W ;
FEIGEN, GA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1961, 5 (04) :299-&
[5]   FLUORESCENCE POLARIZATION IN IMMUNOCHEMISTRY [J].
DANDLIKER, WB ;
SAUSSURE, VA .
IMMUNOCHEMISTRY, 1970, 7 (09) :799-+
[6]   APPLICATION OF FLUORESCENCE ENERGY-TRANSFER AND POLARIZATION TO MONITOR ESCHERICHIA-COLI CAMP RECEPTOR PROTEIN AND LAC PROMOTER INTERACTION [J].
HEYDUK, T ;
LEE, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (05) :1744-1748
[7]  
JOLLEY ME, 1981, CLIN CHEM, V27, P1190
[9]  
Lakowicz J. R., 2010, PRINCIPLES FLUORESCE
[10]   FLUORESCENCE ANISOTROPY ASSAYS IMPLICATE PROTEIN-PROTEIN INTERACTIONS IN REGULATING TRP REPRESSOR DNA-BINDING [J].
LETILLY, V ;
ROYER, CA .
BIOCHEMISTRY, 1993, 32 (30) :7753-7758