Suppr超能文献

雌激素受体-α/配体的密切关系传递着生物活性的信号。

Intimate estrogen receptor-α/ligand relationships signal biological activity.

机构信息

Department of Physical & Chemical Sciences, University of Canterbury, Christchurch, New Zealand.

Department of Physical & Chemical Sciences, University of Canterbury, Christchurch, New Zealand.

出版信息

Toxicology. 2018 Sep 1;408:80-87. doi: 10.1016/j.tox.2018.07.003. Epub 2018 Jul 6.

Abstract

How does estrogen receptor-α bind its natural ligands - estrogens? How can other molecules mimic estrogens and elicit different estrogenic responses? The answers lie in a complex and intimate chemical biology between ligands and receptor. This delicate interaction at the ligand binding cleft signals, via conformational change, exposure of a specific new charge topography at a second site (Activation Function-2). This, in turn, attracts a regulatory protein which modulates gene expression and controls biological activity.

摘要

雌激素受体-α如何与其天然配体——雌激素结合?其他分子如何模拟雌激素并引发不同的雌激素反应?答案在于配体和受体之间复杂而密切的化学生物学关系。配体结合腔内的这种精细相互作用通过构象变化,在第二位点(激活功能 2)暴露特定的新电荷形貌来进行信号转导。反过来,这吸引了一种调节蛋白,调节基因表达并控制生物活性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验