与疾病相关的SHP2突变体的相位分离是MAPK过活化的基础
Guangya Zhu1, Jingjing Xie1, Wenna Kong1
1Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 201203, China; University of the Chinese Academy of Sciences, Beijing 100049, China.
Cell
|October 1, 2020
概括
与疾病相关的SHP2突变通过促进液态相分离 (LLPS) 导致发育障碍. 抑制SHP2LLPS可恢复蛋白质氨酸酶 (PTP) 的活性,并可为这些疾病提供治疗策略.
科学领域:
- 生物化学
- 分子生物学
- 遗传学
背景情况:
- SHP2 (PTPN11) 是一种非受体蛋白氨酸酶,对发育中的RAS-MAPK信号至关重要.
- 激活和非激活PTPN11突变导致重叠的发育障碍,这种悖论无法单独通过酶活性来解释.
研究的目的:
- 研究液态相分离 (LLPS) 在SHP2相关发育障碍中的作用.
- 确定LLPS是否是疾病相关的SHP2突变的常见机制.
- 探索SHP2LLPS的治疗向.
主要方法:
- 使用LLPS试验分析SHP2突变者的行为.
- 研究了PTP域在SHP2LLPS中的作用.
- 评估了全抑制剂对SHP2LLPS和活性的影响.
- 在LLPS凝聚物中研究了突变型和野生型SHP2之间的相互作用.
主要成果:
- 与疾病相关的SHP2突变表现出由PTP域介导的常见LLPS行为.
- 通过自身抑制机制调节SHP2LLPS,并且可以通过全抑制剂减弱,增强PTP活性.
- 在LLPS中突变的SHP2可以招募和激活野生类型的SHP2,促进MAPK信号传递.
结论:
- 在与SHP2相关的人类疾病中,LLPS充当功能增强机制.
- LLPS是蛋白质氨酸酸酶 (PTP) 的新型调节机制.
- 针对SHP2LLPS是一个潜在的治疗策略,用于发育障碍.
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