BTB E3 连接酶 KEAP1 的双价抑制剂能瞬间激活 NRF2 以抑制急性炎症反应

IF 6.6 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mengchen Lu , Jianai Ji , Yifei Lv , Jing Zhao , Yuting Liu , Qiong Jiao , Tian Liu , Yi Mou , Qidong You , Zhengyu Jiang
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引用次数: 0

摘要

大多数含 BTB 的 E3 连接酶都是同源二聚体,通过与多个脱胶子接合来识别单一底物,E3 连接酶 KEAP1 二聚体及其底物 NRF2 就是其中的代表。使 KEAP1 失活以阻碍泛素依赖性 NRF2 降解,从而激活 NRF2。虽然已报道了多种 KEAP1 抑制剂,但所有报道的抑制剂都以单价方式与 KEAP1 结合,并以滞后方式激活 NRF2。在此,我们报告了一种独特的二价 KEAP1 抑制剂 biKEAP1 (3),它能与细胞 KEAP1 二聚体结合,直接释放被螯合的 NRF2 蛋白,从而立即激活 NRF2。3 能促进 NRF2 的核转位,直接抑制促炎细胞因子的转录。体内实验数据显示,3 以前所未有的效力及时减轻了多个急性炎症模型的急性炎症负担。我们的研究结果表明,二价 KEAP1 抑制剂能直接使螯合底物 NRF2 抑制炎症转录反应,减轻各种急性炎症损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bivalent inhibitors of the BTB E3 ligase KEAP1 enable instant NRF2 activation to suppress acute inflammatory response

Bivalent inhibitors of the BTB E3 ligase KEAP1 enable instant NRF2 activation to suppress acute inflammatory response

Bivalent inhibitors of the BTB E3 ligase KEAP1 enable instant NRF2 activation to suppress acute inflammatory response

Most BTB-containing E3 ligases homodimerize to recognize a single substrate by engaging multiple degrons, represented by E3 ligase KEAP1 dimer and its substrate NRF2. Inactivating KEAP1 to hinder ubiquitination-dependent NRF2 degradation activates NRF2. While various KEAP1 inhibitors have been reported, all reported inhibitors bind to KEAP1 in a monovalent fashion and activate NRF2 in a lagging manner. Herein, we report a unique bivalent KEAP1 inhibitor, biKEAP1 (3), that engages cellular KEAP1 dimer to directly release sequestered NRF2 protein, leading to an instant NRF2 activation. 3 promotes the nuclear translocation of NRF2, directly suppressing proinflammatory cytokine transcription. Data from in vivo experiments showed that 3, with unprecedented potency, reduced acute inflammatory burden in several acute inflammation models in a timely manner. Our findings demonstrate that the bivalent KEAP1 inhibitor can directly enable sequestered substrate NRF2 to suppress inflammatory transcription response and dampen various acute inflammation injuries.

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来源期刊
Cell Chemical Biology
Cell Chemical Biology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
14.70
自引率
2.30%
发文量
143
期刊介绍: Cell Chemical Biology, a Cell Press journal established in 1994 as Chemistry & Biology, focuses on publishing crucial advances in chemical biology research with broad appeal to our diverse community, spanning basic scientists to clinicians. Pioneering investigations at the chemistry-biology interface, the journal fosters collaboration between these disciplines. We encourage submissions providing significant conceptual advancements of broad interest across chemical, biological, clinical, and related fields. Particularly sought are articles utilizing chemical tools to perturb, visualize, and measure biological systems, offering unique insights into molecular mechanisms, disease biology, and therapeutics.
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