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通过定量磷酸化蛋白质组学对肌肉特异性激酶信号进行全局分析。

Global analysis of muscle-specific kinase signaling by quantitative phosphoproteomics.

作者信息

Dürnberger Gerhard, Camurdanoglu Bahar Z, Tomschik Matthias, Schutzbier Michael, Roitinger Elisabeth, Hudecz Otto, Mechtler Karl, Herbst Ruth

机构信息

From the ‡Gregor Mendel Institute of Molecular Plant Biology, Dr. Bohr-Gasse 3, 1030 Vienna, Austria; §Institute for Molecular Pathology (IMP), Dr. Bohr-Gasse 7, 1030 Vienna, Austria; ¶Institute of Molecular Biotechnology (IMBA), Dr. Bohr-Gasse 3, 1030 Vienna, Austria;

‖Center for Brain Research, Medical University of Vienna, Spitalgasse 4, 1090 Vienna, Austria;

出版信息

Mol Cell Proteomics. 2014 Aug;13(8):1993-2003. doi: 10.1074/mcp.M113.036087. Epub 2014 Jun 4.

Abstract

The development of the neuromuscular synapse depends on signaling processes that involve protein phosphorylation as a crucial regulatory event. Muscle-specific kinase (MuSK) is the key signaling molecule at the neuromuscular synapse whose activity is required for the formation of a mature and functional synapse. However, the signaling cascade downstream of MuSK and the regulation of the different components are still poorly understood. In this study we used a quantitative phosphoproteomics approach to study the phosphorylation events and their temporal regulation downstream of MuSK. We identified a total of 10,183 phosphopeptides, of which 203 were significantly up- or down-regulated. Regulated phosphopeptides were classified into four different clusters according to their temporal profiles. Within these clusters we found an overrepresentation of specific protein classes associated with different cellular functions. In particular, we found an enrichment of regulated phosphoproteins involved in posttranscriptional mechanisms and in cytoskeletal organization. These findings provide novel insights into the complex signaling network downstream of MuSK and form the basis for future mechanistic studies.

摘要

神经肌肉突触的发育依赖于信号传导过程,其中蛋白质磷酸化作为关键的调节事件参与其中。肌肉特异性激酶(MuSK)是神经肌肉突触处的关键信号分子,其活性对于成熟且功能正常的突触形成是必需的。然而,MuSK下游的信号级联反应以及不同组分的调节仍知之甚少。在本研究中,我们使用定量磷酸化蛋白质组学方法来研究MuSK下游的磷酸化事件及其时间调控。我们总共鉴定出10,183个磷酸肽段,其中203个有显著的上调或下调。根据其时间分布,受调控的磷酸肽段被分为四个不同的簇。在这些簇中,我们发现与不同细胞功能相关的特定蛋白质类别存在过度富集。特别是,我们发现参与转录后机制和细胞骨架组织的受调控磷酸化蛋白质有所富集。这些发现为MuSK下游复杂的信号网络提供了新的见解,并为未来的机制研究奠定了基础。

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