کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2028981 | 1070459 | 2008 | 10 صفحه PDF | دانلود رایگان |
Conjugated equine estrogens (CEEs) are routinely used for hormone replacement therapy (HRT), making it important to understand the activities of individual estrogenic components. Although 17β-estradiol (17β-E2), the most potent estrogen in CEE, has been extensively characterized, the actions of nine additional less potent estrogens are not well understood. Structural differences between CEEs and 17β-E2 result in altered interactions with the two estrogen receptors (ERα and ERβ) and different biological activities. To better understand these interactions, we have determined the crystal structure of the CEE analog, 17β-methyl-17α-dihydroequilenin (NCI 122), in complex with the ERα ligand-binding domain and a peptide from the glucocorticoid receptor-interacting protein 1 (GRIP1) coactivator. NCI 122 has chemical properties, including an unsaturated B-ring and 17α-hydroxyl group, which are shared with some of the estrogens found in CEEs. Structural analysis of the NCI 122–ERα LBD–GRIP1 complex, combined with biochemical and cell-based comparisons of CEE components, suggests that factors such as decreased ligand flexibility, decreased ligand hydrophobicity and loss of a hydrogen bond between the 17-hydroxyl group and His524, contribute significantly to the reduced potency of CEEs on ERα.
Journal: Steroids - Volume 73, Issue 1, January 2008, Pages 59–68