前列腺素作为类固醇受体辅激剂1 (SRC1) 的每-ARNT-Sim (PAS) 域的候选配体
Nicolas Daffern1, Kade Kelley1, José A Villegas2
1Department of Molecular Biosciences, Northwestern University, Evanston, IL 60208.
bioRxiv : the preprint server for biology
|July 28, 2023
概括
类固醇受体协活性剂 (SRCs) 将前列腺素 (PGs) 结合到它们的PAS-B域. 这种相互作用,发生非共价或共价,可能调节转录因子结合.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 类固醇受体协活性剂 (SRCs) 是由真核生物中的转录因子招募的关键蛋白质.
- SRC蛋白质含有参与小分子结合和相互作用调节的双联Per-ARNT-Sim (PAS) 域.
研究的目的:
- 研究SRC1 PAS-B域与前列腺素 (PGs) 之间的相互作用.
- 阐明结合机制及其对转录激活的潜在监管影响.
主要方法:
- 计算式对接方式
- 解决方案核磁共振 (NMR) 光谱学
- 质谱测量质量谱测量
- 分子动力学模拟的模拟.
主要成果:
- 在SRC1 PAS-B域绑定某些前列腺素 (PGs).
- 结合发生在与转录因子结合部位重叠的表面上非共价.
- 还观察到对特定的氨酸残留物的共价结合,该残留物与疏水性口袋相邻.
- 这个口袋靠近,但在正反侧,正规的转录因子结合部位.
结论:
- 对SRC1 PAS-B域的前列腺素结合呈现出一种新的调节机制.
- 这种相互作用表明了调节转录激活剂-协同激活剂动态的潜在途径.
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