| 磷酸化调控泛素单体与Rad23A/Ubiquilin-1中泛素结合域互作的检测 |
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| 引用本文： | 冉梦琳,覃凌云,唐淳,董旭. 磷酸化调控泛素单体与Rad23A/Ubiquilin-1中泛素结合域互作的检测[J]. 波谱学杂志, 2019, 36(1): 15-22. DOI: 10.11938/cjmr20182652 |
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| 作者姓名： | 冉梦琳 覃凌云 唐淳 董旭 |
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| 作者单位： | 波谱与原子分子物理国家重点实验室,武汉磁共振中心(中国科学院武汉物理与数学研究所),湖北武汉430071;中国科学院大学,北京100049;波谱与原子分子物理国家重点实验室,武汉磁共振中心(中国科学院武汉物理与数学研究所),湖北武汉430071 |
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| 基金项目： | 国家重点研究计划资助项目（2017YFA0505400）． |
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| 摘 要： | 泛素(ubiquitin,Ub)是一种广泛存在、高度保守的信号蛋白质,它能够特异性识别成千上万种靶蛋白,以非共价方式行使不同的功能,其中包含蛋白质降解.Ubiquilin-1(Ubql-1)和Rad23A作为两种蛋白降解的转运因子,都包含有与泛素结合的结构域,被称为泛素结合域(ubiquitin-associated domain, UBA).2014年,泛素S65位磷酸化修饰的特异性激酶PINK1被发现,磷酸化使泛素在溶液中呈现舒展态与收缩态两种互相转换的构象.本文通过核磁共振(nuclear magnetic resonance, NMR)技术对UBA和磷酸化泛素之间的相互作用进行检测,观测磷酸化对UBA和泛素结合的影响.实验结果表明Rad23A-UBA2与Ubql-1 UBA都特异性的与磷酸化泛素的舒展态相互作用,但是磷酸化未改变泛素与UBA之间的亲和力.值得注意的是与Ubql-1 UBA相互作用时,磷酸化促进了泛素收缩态向舒展态的转换.
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| 关 键 词： | 泛素(Ub) 磷酸化 核磁共振(NMR) 蛋白质之间相互作用 泛素结合域(UBA) |
| 收稿时间： | 2018-05-18 |
Regulation of Inter-Protein Interactions Between Ubiquitin and Ubiquitin-Associated Domains in Rad23A/Ubiquilin-1 by Phosphorylation |
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| RAN Meng-lin,QIN Ling-yun,TANG Chun,DONG Xu. Regulation of Inter-Protein Interactions Between Ubiquitin and Ubiquitin-Associated Domains in Rad23A/Ubiquilin-1 by Phosphorylation[J]. Chinese Journal of Magnetic Resonance, 2019, 36(1): 15-22. DOI: 10.11938/cjmr20182652 |
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| Authors: | RAN Meng-lin QIN Ling-yun TANG Chun DONG Xu |
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| Affiliation: | 1. State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, National Center for Magnetic Resonance in Wuhan(Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences), Wuhan 430071, China;2. University of Chinese Academy of Sciences, Beijing 100049, China |
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| Abstract: | Ubiquitin is a conserved signaling protein. It is able to interact with thousands of target proteins specifically and perform its biological functions via non-covalent interactions. Ubiquilin-1 (Ubql-1) and Rad23A are two transport factors in the protein-degradation process, and both contain ubiquitin-associated domains (UBAs). S65 of the ubiquitin can be phosphorylated specifically by the kinase PINK1, and the phosphorylated ubiquitin has two interchangeable conformations in solution, the relaxed conformation and the retracted conformation. In this work, nuclear magnetic resonance (NMR) methods were used to characterize the regulation of interactions between the ubiquitin and the UBAs of Rad23A/Ubql-1 by phosphorylation. The results indicated that the UBAs selectively interacted with the relaxed conformation of the phosphorylated ubiquitin without affecting the affinity. When interacting with the UBA of Ubql-1, inter-protein binding appeared to be able to promote the transferring from the retracted conformation to the relaxed conformation. |
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| Keywords: | ubiquitin (Ub) phosphorylation nuclear magnetic resonance (NMR) inter-protein interaction ubiquitin-associated domain (UBA) |
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