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ERRγ tethers strongly bisphenol A and 4-α-cumylphenol in an induced-fit manner

Authors :
Hiroyuki Okada
Yoshimitsu Kakuta
Takatoshi Tokunaga
Takamasa Teramoto
Xiaohui Liu
Ayami Matsushima
Yasuyuki Shimohigashi
Source :
Biochemical and Biophysical Research Communications. 373:408-413
Publication Year :
2008
Publisher :
Elsevier BV, 2008.

Abstract

A receptor-binding assay and X-ray crystal structure analysis demonstrated that the endocrine disruptor bisphenol A (BPA) strongly binds to human estrogen-related receptor gamma (ERRgamma). BPA is well anchored to the ligand-binding pocket, forming hydrogen bonds with its two phenol-hydroxyl groups. In this study, we found that 4-alpha-cumylphenol lacking one of its phenol-hydroxyl groups also binds to ERRgamma very strongly. The 2.0 A crystal structure of the 4-alpha-cumylphenol/ERRgamma complex clearly revealed that ERRgamma's Leu345-beta-isopropyl plays a role in the tight binding of 4-alpha-cumylphenol and BPA, rotating in a back-and-forth induced-fit manner.

Details

ISSN :
0006291X
Volume :
373
Database :
OpenAIRE
Journal :
Biochemical and Biophysical Research Communications
Accession number :
edsair.doi.dedup.....298ec6a89be599794edef51d7e91f21c
Full Text :
https://doi.org/10.1016/j.bbrc.2008.06.050