Luminex-based triplex immunoassay for the simultaneous detection of soy, pea, and soluble wheat proteins in milk powder

被引:42
作者
Haasnoot, Willem [1 ]
du Pre, Jolanda G. [1 ]
机构
[1] Wageningen UR, Inst Food Safety, RIKILT, NL-6700 AE Wageningen, Netherlands
关键词
luminex; multiplex; immunoassay; vegetable proteins; soy; pea; soluble wheat proteins; milk powder; adulteration;
D O I
10.1021/jf063281o
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
An automated fluorescent microsphere-based flow cytometric triplex immunoassay, using the Luminex 100 flow analyzer with MultiAnalyte Profiling (xMAP) technology, was developed for the simultaneous detection of proteins from three vegetable sources as potential fraudulent adulterants in milk powder. In the final triplex inhibition immunoassay, soluble wheat proteins (SWP) and proteins from soy and pea were coupled to three different microsphere sets. A mixture of these microsphere sets was transferred to a microtiter plate well together with the sample and a mixture of three affinity-purified polyclonal antibodies raised against the proteins and labeled with a fluorophore (Alexa 532). After incubation for 1.5 h at room temperature in the dark, the fluorescence intensities on the microspheres were directly measured (no wash procedure) in the Luminex during 10 s per well (100 microspheres per set). The sensitivities of the three assays for plant protein extracts were determined as 0.5-0.6 mu g/mL at 50% inhibition. For the detection of the vegetable proteins in milk powder, the samples were dissolved in buffer (0.1 g in 10 mL) and further diluted (20 times) to create a 50% inhibition at approximately 0.5% of the vegetable proteins in the total protein content of milk powder. With the help of calibration standards, prepared under conditions comparable to those for sample materials, the triplex immunoassay proved to be quantitative above 0.1%, although concentrations in high-heated milk powders were underestimated. Due to the xMAP technology, in which 100 different microsphere sets can be distinguished, this triplex immunoassay can easily be extended to detect other possible adulterants.
引用
收藏
页码:3771 / 3777
页数:7
相关论文
共 11 条
[1]   Simultaneous detection of antibodies to foot-and-mouth disease non-structural proteins 3ABC, 3D, 3A and 3B by a multiplexed Luminex assay to differentiate infected from vaccinated cattle [J].
Clavijo, A ;
Hole, K ;
Li, MY ;
Collignon, B .
VACCINE, 2006, 24 (10) :1693-1704
[2]   A comparison of ELISA and flow micro sphere-based assays for quantification of immunoglobulins [J].
Dasso, J ;
Lee, J ;
Bach, H ;
Mage, RG .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 263 (1-2) :23-33
[3]   Applications of Luminex® xMAP™ technology for rapid, high-throughput multiplexed nucleic acid detection [J].
Dunbar, SA .
CLINICA CHIMICA ACTA, 2006, 363 (1-2) :71-82
[4]   Direct biosensor immunoassays for the detection of nonmilk proteins in milk powder [J].
Haasnoot, W ;
Olieman, K ;
Cazemier, G ;
Verheijen, R .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (11) :5201-5206
[5]  
Kettman JR, 1998, CYTOMETRY, V33, P234, DOI 10.1002/(SICI)1097-0320(19981001)33:2<234::AID-CYTO19>3.0.CO
[6]  
2-V
[7]  
Manso M. A., 2002, Bulletin of the International Dairy Federation, P25
[8]  
Manso MA, 2002, J AOAC INT, V85, P1090
[9]  
*MOL PROB INC, 2004, PROD INF
[10]   Comparison of multiplexed techniques for detection of bacterial and viral proteins [J].
Rao, RS ;
Visuri, SR ;
McBride, MT ;
Albala, JS ;
Matthews, DL ;
Coleman, MA .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (04) :736-742