化学
可药性
突变体
光解
质谱法
生物物理学
突变
共价键
蛋白质结构
GTP酶
紫外线
立体化学
结晶学
生物化学
构象变化
罗亚
结构生物学
紫外线
GTP'
超家族
蛋白质-蛋白质相互作用
作者
Haozhe Wu,Zheyi Liu,Haibo Jiang,Heng Zhao,Chen Dong,Yu Lu,Shijia Zu,Yongjie Guo,Can Lai,Pan Luo,Ke Xu,Yuxin Yang,Yafang Yang,Zhongya Sun,Qingcheng Huang,Huan Xiong,Lanxin Zhou,Yipan Luo,Yuhan Zeng,Daohai Du
摘要
Pathogenic mutations in “undruggable” Ras superfamily proteins challenge drug development by inducing subtle, dynamic conformational changes. Here, we integrated X-ray crystallography with native mass spectrometry and ultraviolet photodissociation (nMS-UVPD) to reveal a cryptic conformation in the oncogenic Y42C mutant of RhoA. While crystallography alone resolved two ambiguous structures, nMS-UVPD determined the dominant conformation by directly mapping the mutant’s conformational dynamics, identifying an enhanced Mg2+-locked conformation. We explored the mechanism of mutation impairing GTP hydrolysis. This state unmasks a previously hidden, druggable pocket adjacent to Cys42, guiding our identification of a covalent inhibitor. Our integrated approach establishes a roadmap for targeting pathogenic protein mutants previously considered “undruggable” due to their highly dynamic nature.
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