变构调节
化学
抑制器
生物物理学
DNA
转录因子
抄写(语言学)
分子动力学
机制(生物学)
细胞生物学
动力学(音乐)
功能(生物学)
变构酶
结合位点
计算生物学
突变
血浆蛋白结合
动力学
DNA损伤
残留物(化学)
构象变化
蛋白质-蛋白质相互作用
过渡(遗传学)
氢键
DNA结合域
蛋白质结构
能源景观
生物化学
DNA修复
分子开关
转录调控
循环(图论)
蛋白质动力学
立体化学
蛋白质结构域
作者
Pablo Navarro Acero,Ming‐Hong Hao,Karan Kapoor
标识
DOI:10.1021/acs.jcim.5c02227
摘要
The tumor suppressor p53 regulates transcription in response to cellular stress, with mutations in its DNA-binding domain (DBD) found in most human cancers. The L1 loop within the DBD is believed to play a critical role in DNA recognition, yet its conformational dynamics remain poorly understood. Using enhanced molecular dynamics simulations combined with machine learning-derived collective variables, we reveal a novel conformational switch mechanism governing p53's DNA-binding activity. Our analysis identifies two distinct transition pathways between extended (DNA-binding competent) and recessed conformations, each characterized by specific hydrogen bond networks and high energy barriers. We discovered a potential allosteric mechanism regulating the DNA-p53 binding interface that could provide an atomistic basis for gene-specific transcription regulation. This mechanism would explain the prevalence of certain cancer mutations, particularly at residue R282. Finally, we provide a mechanistic rationale for how compounds targeting a reactivation pocket near the L1 loop may restore p53 function by modulating DNA binding kinetics rather than affinity, thereby reconciling previously observed rescue effects.
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