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Facile screening of potential xenoestrogens by an estrogen receptor-based reusable optical biosensor.

Authors :
Liu, Lanhua
Zhou, Xiaohong
Lu, Yun
Shan, Didi
Xu, Bi
He, Miao
Shi, Hanchang
Qian, Yi
Source :
Biosensors & Bioelectronics. Nov2017, Vol. 97, p16-20. 5p.
Publication Year :
2017

Abstract

The apparent increase in hormone-induced cancers and disorders of the reproductive tract has led to a growing demand for new technologies capable of screening xenoestrogens. We reported an estrogen receptor (ER)-based reusable fiber biosensor for facile screening estrogenic compounds in environment. The bioassay is based on the competition of xenoestrogens with 17β-estradiol (E 2 ) for binding to the recombinant receptor of human estrogen receptor α (hERα) protein, leaving E 2 free to bind to fluorophore-labeled anti–E 2 monoclonal antibody. Unbound anti–E 2 antibody then binds to the immobilized E 2 –protein conjugate on the fiber surface, and is detected by fluorescence emission induced by evanescent field. As expected, the stronger estrogenic activity of xenoestrogen would result in the weaker fluorescent signal. Three estrogen-agonist compounds, diethylstilbestrol (DES), 4-n-nonylphenol (NP) and 4-n-octylphenol (OP), were chosen as a paradigm for validation of this assay. The rank order of estrogenic potency determined by this biosensor was DES>OP>NP, which were consistent with the published results in numerous studies. Moreover, the E 2 –protein conjugate modified optical fiber was robust enough for over 300 sensing cycles with the signal recoveries ranging from 90% to 100%. In conclusion, the biosensor is reusable, reliable, portable and amenable to on-line operation, providing a facile, efficient and economical alternative to screen potential xenoestrogens in environment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09565663
Volume :
97
Database :
Academic Search Index
Journal :
Biosensors & Bioelectronics
Publication Type :
Academic Journal
Accession number :
123814946
Full Text :
https://doi.org/10.1016/j.bios.2017.05.026