Ottawa Institute of Systems Biology, University of Ottawa, Ottawa, Ontario, Canada K1H 8M5.
Mol Cell Proteomics. 2011 Nov;10(11):M110.007252. doi: 10.1074/mcp.M110.007252. Epub 2011 Aug 22.
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.
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。