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Development of a chemiluminometric immunosensor array for on-site monitoring of genetically modified organisms

Authors
Jang, Hye-JeeCho, Il-HoonKim, Hee-SooJeon, Jin-WooHwang, Se-YoungPaek, Se-Hwan
Issue Date
20-7월-2011
Publisher
ELSEVIER SCIENCE SA
Keywords
Genetically modified organisms; Marker proteins; Sandwich-type immunoassys; Chemiluminometric signal; Photodiode array
Citation
SENSORS AND ACTUATORS B-CHEMICAL, v.155, no.2, pp.598 - 605
Indexed
SCIE
SCOPUS
Journal Title
SENSORS AND ACTUATORS B-CHEMICAL
Volume
155
Number
2
Start Page
598
End Page
605
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/111974
DOI
10.1016/j.snb.2011.01.016
ISSN
0925-4005
Abstract
Genetically modified organisms (GMOs) have been mainly developed for mass production of agricultural plants; however, there are concerns that transgenic crops might cause side effects on ecosystems and human beings. Therefore, to quantitatively trace the genetically modified products, we constructed a chemiluminometric immunosensor array for the detection of recombinant marker proteins expressed in GMOs, i.e., 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS), neomycin phosphotransferase II (NPT II), and phophinothricin acethyltransferase (PAT). Monoclonal and polyclonal antibodies specific to each marker were raised, and the specificities and immunoreactivities to the respective markers were characterized. The capture antibodies were immobilized on predetermined regions of a glass slide where the sandwich-type immunoassays were carried out. Photodiodes were located on the bottom of the slide in an aligned arrangement to the immobilized antibody sites such that the light signals resulting from the immunoassays could be detected in situ. Under optimal conditions, the immunosensors were able to detect 1% GMO marked with EPSPS, which was the minimum content over the total content, and 3% GMOs labeled with NPT lot PAT. The sensor array developed in this study would be useful for measuring a particular GMO in a specimen containing unidentified species. (C) 2011 Elsevier B.V. All rights reserved.
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