THE BINDING OF ESTROGEN AND ESTROGEN ANTAGONISTS TO THE ESTROGEN-RECEPTOR

被引:4
作者
BOND, JP
SASSON, S
NOTIDES, AC
机构
[1] UNIV ROCHESTER, SCH MED & DENT, DEPT BIOPHYS, ROCHESTER, NY 14642 USA
[2] HEBREW UNIV JERUSALEM, SCH MED, DEPT PHARMACOL, IL-91010 JERUSALEM, ISRAEL
关键词
D O I
10.1016/0003-9861(92)90614-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The model of the estrogen receptor as a dimer of identical, interacting subunits and data obtained by Sasson and Notides (1988, Mol. Endocrinol. 2, 307-312) were used to find the standard free energy changes that describe the binding of estradiol and 4-hydroxytamoxifen to the estrogen receptor. For the binding of estradiol or 4-hydroxytamoxifen to the estrogen receptor the data do not deviate systematically from the best fit to the model. The standard free energy change for binding of one molecule of estradiol at one site and one molecule of 4-hydroxytamoxifen at the second site of estrogen receptor indicates that 4-hydroxytamoxifen antagonizes the binding of estradiol to the estrogen receptor. © 1992.
引用
收藏
页码:583 / 591
页数:9
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