Wagner R L, Apriletti J W, McGrath M E, West B L, Baxter J D, Fletterick R J
Graduate Group in Biophysics, University of California at San Francisco 94143-0448, USA.
Nature. 1995 Dec 14;378(6558):690-7. doi: 10.1038/378690a0.
The crystal structure of the rat alpha 1 thyroid hormone receptor ligand-binding domain bound with a thyroid hormone agonist reveals that ligand is completely buried within the domain as part of the hydrophobic core. In addition, the carboxy-terminal activation domain forms an amphipathic helix, with its hydrophobic face constituting part of the hormone binding cavity. These observations suggest a structural role for ligand, in establishing the active conformation of the receptor, that is likely to underlie hormonal regulation of gene expression for the nuclear receptors.
与甲状腺激素激动剂结合的大鼠α1甲状腺激素受体配体结合域的晶体结构表明,配体作为疏水核心的一部分完全埋藏在该结构域内。此外,羧基末端激活结构域形成一个两亲性螺旋,其疏水面构成激素结合腔的一部分。这些观察结果表明配体在建立受体活性构象中具有结构作用,这可能是核受体基因表达激素调节的基础。