紊乱的c端在小GTPase Ran的活性中起关键作用。

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biochemistry Biochemistry Pub Date : 2025-03-18 Epub Date: 2025-02-25 DOI:10.1021/acs.biochem.4c00484
Wenyuan Wei, Melissa Valerio, Ning Ma, Hyunjun Kang, Le Xuan Truong Nguyen, Guido Marcucci, Nagarajan Vaidehi
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引用次数: 0

摘要

Ran是Ras超家族中的一个小GTPase,它控制核胞质转运,包括miR-126,一种支持白血病干细胞(LSCs)稳态和扩增的microRNA。Ran与Exportin 5结合,促进前体(pre)-miR-126通过核膜的运输,使其成熟。我们的目标是抑制Ran以阻止pre-miR-126向细胞质的运输。与其他Ras家族蛋白一样,由于Ran表面相对平坦且缺乏结合空腔,用小分子靶向Ran具有挑战性。Ran的活性受一个长而无序的c端调控,这为识别潜在的结合袋提供了机会。我们采用分子动力学模拟和实验相结合的方法,揭示了c端构象集合的关键作用,使Ran从gtp结合的“开状态”转变为gdp结合的“关状态”。我们还发现Ran c端可变地调节核苷酸结合位点和功能相关的Switch 1和2区域残基的构象。通过计算深度突变扫描和实验,我们确定了核心- c端界面的4个残基热点L182、Y197、D200和L201,以及介导核心和开关区之间变弹性通信的4个残基突变V27A、E70D、N122A和N122Y。这一信息为我们下一步设计新型Ran变构调制器铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disordered C-Terminus Plays a Critical Role in the Activity of the Small GTPase Ran.

Ran is a small GTPase of the Ras superfamily that governs nucleocytoplasmic transport, including that of miR-126, a microRNA that supports the homeostasis and expansion of leukemia stem cells (LSCs). Ran binds to Exportin 5 to facilitate the transport of precursor (pre)-miR-126 across the nuclear membrane for its maturation. Our goal is to inhibit Ran to prevent transport of pre-miR-126 to the cytoplasm. Like other Ras family proteins, targeting Ran with small molecules is challenging due to its relatively flat surface and lack of binding cavities. Ran's activity is regulated by a long and disordered C-terminus that provides opportunities for identifying cryptic binding pockets to target. We used a combination of molecular dynamics simulations and experiments and uncovered the critical role of the ensemble of the C-terminal conformations that enable the transition of Ran from the GTP-bound "on state" to its GDP-bound "off-state". We also showed that the Ran C-terminus allosterically modulates the conformations of residues in the nucleotide binding site and in the functionally relevant Switch 1 and 2 regions. Through computational deep mutational scans and experiments, we identified four residue hotspots L182, Y197, D200, and L201 at the core-C-terminus interface and four residue mutations V27A, E70D, N122A, and N122Y that mediate the allosteric communication between the core and switch regions. This information paves the way for our next step in the design of novel allosteric modulators for Ran.

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来源期刊
Biochemistry Biochemistry
Biochemistry Biochemistry 生物-生化与分子生物学
CiteScore
5.50
自引率
3.40%
发文量
336
审稿时长
1-2 weeks
期刊介绍: Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.
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