酸化依赖的伪酶域二分化驱动全长MLKL寡合化
Yanxiang Meng1,2, Sarah E Garnish1,2, Katherine A Davies1,2
1Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, VIC, 3052, Australia.
Nature communications
|October 26, 2023
概括
亡细胞死亡依赖于RIPK3激酶激活MLKL. 这项研究揭示了RIPK3酸化触发MLKL二度化和四度化,这对于膜透和细胞死亡至关重要.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 亡是一种亲炎性细胞死亡途径,与各种人类疾病有关.
- 死亡亡的终端阶段,涉及RIPK3激酶和MLKL,尚未完全理解.
研究的目的:
- 从结构上阐明RIPK的MLKL激活机制3.
- 了解MLKL的寡合化如何导致细胞膜透.
主要方法:
- 负染色电子显微镜的电子显微镜.
- 结构建模 结构建模
- 突变分析 突变分析
主要成果:
- 通过RIPK3介导的酸化会诱导MLKL伪激酶域的二分化.
- MLKL的二元化驱动了延长型同位基的形成.
- 在MLKL内部的一个中央卷轴卷轴核化了四聚体组件,先于膜通透.
结论:
- MLKL四重化是其破坏膜功能的关键先决条件.
- 了解MLKL激活提供了对亡相关疾病的见解.
- 结构细节揭示了RIPK3激酶激活MLKL的机制.
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