辅活化剂
核受体辅活化子2
核受体辅活化子3
核受体
核受体辅活化子1
生物
雌激素相关受体γ
雌激素相关受体α
神经元源性孤儿受体1
核受体辅阻遏物1
细胞生物学
受体
酶联受体
转录因子
5-HT5A受体
毛皮-1
雌激素受体
遗传学
基因
癌症
乳腺癌
作者
Stéphanie Gaillard,Mary A. Dwyer,Donald P. McDonnell
摘要
Abstract Estrogen receptor-related receptor-α (ERRα) is an orphan nuclear receptor that does not appear to require a classical small molecule ligand to facilitate its interaction with coactivators and/or hormone response elements within target genes. Instead, the apo-receptor is capable of interacting in a constitutive manner with coactivators that stimulate transcription by acting as protein ligands. We have screened combinatorial phage libraries for peptides that selectively interact with ERRα to probe the architecture of the ERRα-coactivator pocket. In this manner, we have uncovered a fundamental difference in the mechanism by which this receptor interacts with peroxisome proliferator-activated receptor-γ coactivator-1α, as compared with members of the steroid receptor coactivator subfamily of coactivators. Our findings suggest that it may be possible to develop ERRα ligands that exhibit different pharmacological activities as a consequence of their ability to differentially regulate coactivator recruitment. In addition, these findings have implications beyond ERRα because they suggest that subtle alterations in the structure of the activation function-2 pocket within any nuclear receptor may enable differential recruitment of coactivators, an observation of notable pharmaceutical importance.
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