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Molecular recognition of endocrine disruptors by synthetic and natural 17β-estradiol receptors: a comparative study

Bernadette Tse Sum Bui ,  Karsten Haupt 

Compiegne University of Technology, UMR CNRS 6022, Compiegne, France

Abstract

A β-estradiol receptor binding mimic was synthesized using molecular imprinting. Polymers (bulk and microgels) were prepared in acetonitrile by using methacrylic acid and ethyleneglycoldimethacrylate as the cross-linker. The selectivity was evaluated by radioligand binding assays. The imprinted polymers were very specific to β-estradiol since the control polymers bound virtually no radioligand. The bulk polymer was employed to screen endocrine disrupting chemicals. Structurally-related steroids like α-estradiol, estrone and ethynylestradiol showed respectively 14, 5 and 0.7 % of cross-reactivities with β-estradiol whereas most unrelated chemicals do not bind at all. These results are compared to those obtained with bioassays using cells in culture bearing β-estradiol-induced genes.

 

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Related papers

Presentation: Poster at SMCBS'2007 International Workshop, by Bernadette Tse Sum Bui
See On-line Journal of SMCBS'2007 International Workshop

Submitted: 2007-09-08 09:38
Revised:   2009-06-07 00:44