核受体的不对称交叉反应性揭示了雌激素和雄激素信号之间的进化缓冲区
bioRxiv : the preprint server for biology
|December 25, 2025
概括
雌激醇比激素更强烈地与雄激素受体结合,揭示了类固醇激素相互作用中的意想不到的不对称性. 这一发现表明雌醇是一种古老的配体,并影响健康和疾病中的受体信号传递.
科学领域:
- 内分泌学 在内分泌学.
- 进化生物学 进化生物学
- 计算生物学 计算生物学
背景情况:
- 类固醇激素受体在生理学和疾病中起着至关重要的作用.
- 了解受体-连接体相互作用是解读激素信号的关键.
- 在类固醇激素结合的不对称性已经很差的特征.
研究的目的:
- 研究各种类固醇及其受体之间的结合亲和关系.
- 发现类固醇激素受体相互作用中的潜在不对称性.
- 探索类固醇受体关系的进化基础.
主要方法:
- 利用Boltz-2,一个深度学习框架,进行全方位的受体-连接体亲和力查.
- 进行了系统的in silico亲和力预测.
- 采用了祖先受体的结构建模和分析.
主要成果:
- 雌激醇对雄激素受体的预测亲和力高于.
- 雌激醇强烈地与多个类固醇激素受体结合,但不是相反.
- 祖先受体的重建表明,雌醇是一种古老的配体.
- 不对称的结合会影响生理和病理信号.
结论:
- 在类固醇激素受体结合中存在未被识别的不对称性,而雌醇显示出广泛的兼容性.
- 雌激醇与受体的古老兼容性与其他类固醇不断变化的特异性形成鲜明对比.
- 这种不对称性为雌激醇提供了一个调节雄激素受体信号的机制,对前列腺癌等疾病有影响.
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