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白细胞介素-1受体相关激酶M死亡结构域:关于三个表面的故事

The IRAK-M death domain: a tale of three surfaces.

作者信息

Gürkan Berke, Poelman Hessel, Pereverzeva Liza, Kruijswijk Danielle, de Vos Alex F, Groenen Anouk G, Nollet Edgar E, Wichapong Kanin, Lutgens Esther, van der Poll Tom, Du Jiangfeng, Wiersinga W Joost, Nicolaes Gerry A F, van 't Veer Cornelis

机构信息

Center of Experimental and Molecular Medicine, Amsterdam UMC Location University of Amsterdam, Amsterdam, Netherlands.

Amsterdam Infection and Immunity Institute, Amsterdam UMC Location University of Amsterdam, Amsterdam, Netherlands.

出版信息

Front Mol Biosci. 2024 Jan 10;10:1265455. doi: 10.3389/fmolb.2023.1265455. eCollection 2023.

Abstract

The anti-inflammatory interleukin-1 receptor associated kinase-M (IRAK-M) is a negative regulator of MyD88/IRAK-4/IRAK-1 signaling. However, IRAK-M has also been reported to activate NF-κB through the MyD88/IRAK-4/IRAK-M myddosome in a MEKK-3 dependent manner. Here we provide support that IRAK-M uses three surfaces of its Death Domain (DD) to activate NF-κB downstream of MyD88/IRAK-4/IRAK-M. Surface 1, with central residue Trp74, binds to MyD88/IRAK-4. Surface 2, with central Lys60, associates with other IRAK-M DDs to form an IRAK-M homotetramer under the MyD88/IRAK-4 scaffold. Surface 3; with central residue Arg97 is located on the opposite side of Trp74 in the IRAK-M DD tetramer, lacks any interaction points with the MyD88/IRAK-4 complex. Although the IRAK-M DD residue Arg97 is not directly involved in the association with MyD88/IRAK-4, Arg97 was responsible for 50% of the NF-κB activation though the MyD88/IRAK-4/IRAK-M myddosome. Arg97 was also found to be pivotal for IRAK-M's interaction with IRAK-1, and important for IRAK-M's interaction with TRAF6. Residue Arg97 was responsible for 50% of the NF-κB generated by MyD88/IRAK-4/IRAK-M myddosome in IRAK-1/MEKK3 double knockout cells. By structural modeling we found that the IRAK-M tetramer surface around Arg97 has excellent properties that allow formation of an IRAK-M homo-octamer. This model explains why mutation of Arg97 results in an IRAK-M molecule with increased inhibitory properties: it still binds to myddosome, competing with myddosome IRAK-1 binding, while resulting in less NF-κB formation. The findings further identify the structure-function properties of IRAK-M, which is a potential therapeutic target in inflammatory disease.

摘要

抗炎性白细胞介素-1受体相关激酶-M(IRAK-M)是MyD88/IRAK-4/IRAK-1信号通路的负调节因子。然而,也有报道称IRAK-M可通过MyD88/IRAK-4/IRAK-M髓样分化因子88体,以MEKK-3依赖的方式激活核因子κB(NF-κB)。在此,我们证实IRAK-M利用其死亡结构域(DD)的三个表面在MyD88/IRAK-4/IRAK-M下游激活NF-κB。表面1的中心残基为色氨酸74,与MyD88/IRAK-4结合。表面2的中心残基为赖氨酸60,在MyD88/IRAK-4支架下与其他IRAK-M DD结合形成IRAK-M同四聚体。表面3的中心残基为精氨酸97,位于IRAK-M DD四聚体中色氨酸74的对面,与MyD88/IRAK-4复合物没有任何相互作用点。尽管IRAK-M DD残基精氨酸97不直接参与与MyD88/IRAK-4的结合,但精氨酸97通过MyD88/IRAK-4/IRAK-M髓样分化因子88体导致50%的NF-κB激活。还发现精氨酸97对IRAK-M与IRAK-1的相互作用至关重要,对IRAK-M与肿瘤坏死因子受体相关因子6(TRAF6)的相互作用也很重要。在IRAK-1/MEKK3双敲除细胞中,残基精氨酸97导致MyD88/IRAK-4/IRAK-M髓样分化因子88体产生50%的NF-κB。通过结构建模,我们发现精氨酸97周围的IRAK-M四聚体表面具有优异的特性,能够形成IRAK-M同八聚体。该模型解释了为什么精氨酸97的突变会导致具有增强抑制特性的IRAK-M分子:它仍然与髓样分化因子88体结合,与髓样分化因子88体中IRAK-1的结合竞争,同时导致较少的NF-κB形成。这些发现进一步确定了IRAK-M的结构-功能特性,其是炎性疾病中的一个潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0963/10806146/e270f1f1f0fd/fmolb-10-1265455-g001.jpg

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