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Ran 结合蛋白 RanBPM 可以通过与 TRAF6 相互作用来抑制 NF-κB 通路。

The Ran-binding protein RanBPM can depress the NF-κB pathway by interacting with TRAF6.

机构信息

Department of Biochemistry and Molecular Biology, National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, 5 Dong Dan San Tiao St, Beijing, 100005, China.

出版信息

Mol Cell Biochem. 2012 Jan;359(1-2):83-94. doi: 10.1007/s11010-011-1002-3. Epub 2011 Jul 30.

Abstract

Ran-binding protein in microtubule-organizing center (RanBPM) has been reported to interact with the neurotrophin receptors p75NTR and TrkA, meanwhile p75NTR and TrkA can also interact with TRAF6. Whether RanBPM interacts directly with TRAF6 has not yet been established. In this study, using a yeast two-hybrid system and glutathione-S: -transferase pull-down assays, we determined that RanBPM binds to the TRAF6 C-terminus through its SPRY motif. Complex formation between overexpressed RanBPM and TRAF6 was also confirmed with a co-immunoprecipitation assay, laser scanning confocal and fluorescence resonance energy transfer. Additional co-immunoprecipitation experiments verified that endogenous RanBPM and TRAF6 interact in several mammalian cell lines. A series of experiments revealed that RanBPM influences TRAF6 ubiquitination and the TRAF6-triggered NF-κB signaling pathway through RanBPM's interaction with TRAF6. These data suggest that RanBPM participates in gene transcription by binding to TRAF6.

摘要

微管组织中心中的 Ran 结合蛋白(RanBPM)已被报道与神经营养因子受体 p75NTR 和 TrkA 相互作用,同时 p75NTR 和 TrkA 也可以与 TRAF6 相互作用。然而,RanBPM 是否直接与 TRAF6 相互作用尚未确定。在这项研究中,我们使用酵母双杂交系统和谷胱甘肽 S-转移酶下拉测定法,确定 RanBPM 通过其 SPRY 基序与 TRAF6 的 C 末端结合。通过共免疫沉淀实验、激光扫描共聚焦和荧光共振能量转移实验也证实了过表达的 RanBPM 和 TRAF6 之间的复合物形成。另外的共免疫沉淀实验验证了内源性 RanBPM 和 TRAF6 在几种哺乳动物细胞系中相互作用。一系列实验表明,RanBPM 通过与 TRAF6 的相互作用影响 TRAF6 的泛素化和 TRAF6 触发的 NF-κB 信号通路。这些数据表明,RanBPM 通过与 TRAF6 结合参与基因转录。

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