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利用 AutoProteome 系统揭示主生物钟对光的蛋白质组反应。

Uncovering the proteome response of the master circadian clock to light using an AutoProteome system.

机构信息

Ottawa Institute of Systems Biology, University of Ottawa, Ottawa, Ontario, Canada K1H 8M5.

出版信息

Mol Cell Proteomics. 2011 Nov;10(11):M110.007252. doi: 10.1074/mcp.M110.007252. Epub 2011 Aug 22.

Abstract

In mammals, the suprachiasmatic nucleus (SCN) is the central circadian pacemaker that governs rhythmic fluctuations in behavior and physiology in a 24-hr cycle and synchronizes them to the external environment by daily resetting in response to light. The bilateral SCN is comprised of a mere ~20,000 neurons serving as cellular oscillators, a fact that has, until now, hindered the systematic study of the SCN on a global proteome level. Here we developed a fully automated and integrated proteomics platform, termed AutoProteome system, for an in-depth analysis of the light-responsive proteome of the murine SCN. All requisite steps for a large-scale proteomic study, including preconcentration, buffer exchanging, reduction, alkylation, digestion and online two-dimensional liquid chromatography-tandem MS analysis, are performed automatically on a standard liquid chromatography-MS system. As low as 2 ng of model protein bovine serum albumin and up to 20 μg and 200 μg of SCN proteins can be readily processed and analyzed by this system. From the SCN tissue of a single mouse, we were able to confidently identify 2131 proteins, of which 387 were light-regulated based on a spectral counts quantification approach. Bioinformatics analysis of the light-inducible proteins reveals their diverse distribution in different canonical pathways and their heavy connection in 19 protein interaction networks. The AutoProteome system identified vasopressin-neurophysin 2-copeptin and casein kinase 1 delta, both of which had been previously implicated in clock timing processes, as light-inducible proteins in the SCN. Ras-specific guanine nucleotide-releasing factor 1, ubiquitin protein ligase E3A, and X-linked ubiquitin specific protease 9, none of which had previously been implicated in SCN clock timing processes, were also identified in this study as light-inducible proteins. The AutoProteome system opens a new avenue to systematically explore the proteome-wide events that occur in the SCN, either in response to light or other stimuli, or as a consequence of its intrinsic pacemaker capacity.

摘要

在哺乳动物中,视交叉上核(SCN)是中央生物钟起搏器,它以 24 小时周期控制行为和生理的节律性波动,并通过对光的每日重置来与外部环境同步。双侧 SCN 由大约 20000 个神经元组成,作为细胞振荡器,直到现在,这一事实一直阻碍着对 SCN 进行全局蛋白质组水平的系统研究。在这里,我们开发了一种全自动集成的蛋白质组学平台,称为 AutoProteome 系统,用于深入分析小鼠 SCN 的光响应蛋白质组。大规模蛋白质组学研究的所有必需步骤,包括浓缩、缓冲交换、还原、烷基化、消化和在线二维液相色谱-串联 MS 分析,都在标准液相色谱-MS 系统上自动进行。该系统可以轻松处理和分析低至 2ng 的模型蛋白牛血清白蛋白和高达 20μg 和 200μg 的 SCN 蛋白。从一只老鼠的 SCN 组织中,我们能够自信地鉴定出 2131 种蛋白质,其中 387 种根据光谱计数定量方法是光调节的。对光诱导蛋白的生物信息学分析表明,它们在不同的规范途径中分布广泛,在 19 个蛋白质相互作用网络中连接紧密。AutoProteome 系统鉴定了血管加压素-神经垂体素 2-copeptin 和酪蛋白激酶 1 德尔塔,这两种蛋白以前都被认为与生物钟计时过程有关,是 SCN 中的光诱导蛋白。Ras 特异性鸟嘌呤核苷酸释放因子 1、泛素蛋白连接酶 E3A 和 X 连锁泛素特异性蛋白酶 9,以前都没有被认为与 SCN 时钟计时过程有关,在这项研究中也被鉴定为光诱导蛋白。AutoProteome 系统为系统地探索 SCN 中发生的蛋白质组范围的事件开辟了新途径,无论是对光还是其他刺激的反应,还是其内在生物钟能力的结果。

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