在激活EGF受体的过程中,通过等离子体膜进行符合性合
Nicholas F Endres1, Rahul Das, Adam W Smith
1Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Cell
|February 5, 2013
概括
表皮生长因子受体 (EGFR) 的激活取决于其表面密度. 结合EGF释放了固体约束,促进了跨膜螺旋相互作用和受体激活.
科学领域:
- 生物化学 生物化学
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
背景情况:
- 表皮生长因子受体 (EGFR) 激活机制尚未完全理解.
- 在溶液中,EGFR的细胞内域表现出内在活性.
研究的目的:
- 为了研究EGFR激活的调节.
- 确定EGFR表面密度在自酸化中的作用.
主要方法:
- 测量EGFR自化作为细胞表面密度的函数.
- 光交叉相关谱学以评估二分化.
- 核磁共振 (NMR) 和功能测试.
主要成果:
- 只有在没有EGF的高表面密度下,EGFR才能摆脱抑制.
- 跨膜螺旋和细胞内模块一起使构成性活动成为可能.
- 隔离的细胞内模块是不活跃的,当它被绑在膜上时,它无法二元化.
- 激活需要N端的跨膜螺旋相互作用,促进柔膜段相互作用和膜释放.
结论:
- 结合EGF可以缓解细胞外硬质约束.
- 这促进了跨膜螺旋体通过N端关联的激活.
- EGFR激活由连接体结合和受体表面密度来调节.
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