Division of Clinical Biochemistry, Biocenter, Innsbruck Medical University, A-6020 Innsbruck, Austria.
Mol Cell Proteomics. 2013 Sep;12(9):2640-56. doi: 10.1074/mcp.M112.024109. Epub 2013 May 29.
We present the first comprehensive capillary electrophoresis electrospray ionization mass spectrometry (CESI-MS) analysis of post-translational modifications derived from H1 and core histones. Using a capillary electrophoresis system equipped with a sheathless high-sensitivity porous sprayer and nano-liquid chromatography electrospray ionization mass spectrometry (nano-LC-ESI-MS) as two complementary techniques, we characterized H1 histones isolated from rat testis. Without any pre-separation of the perchloric acid extraction, a total of 70 different modified peptides, including 50 phosphopeptides, were identified in the rat linker histones H1.0, H1a-H1e, and H1t. Out of the 70 modified H1 histone peptides, 27 peptides could be identified with CESI-MS only, and 11 solely with LC-ESI-MS. Immobilized metal-affinity chromatography enrichment prior to MS analysis yielded a total of 55 phosphopeptides; 22 of these peptides could be identified only by CESI-MS, and 19 only by LC-ESI-MS, showing the complementarity of the two techniques. We mapped 42 H1 modification sites, including 31 phosphorylation sites, of which 8 were novel sites. For the analysis of core histones, we chose a different strategy. In a first step, the sulfuric-acid-extracted core histones were pre-separated using reverse-phase high-performance liquid chromatography. Individual rat testis core histone fractions obtained in this way were digested and analyzed via bottom-up CESI-MS. This approach yielded the identification of 42 different modification sites including acetylation (lysine and N(α)-terminal); mono-, di-, and trimethylation; and phosphorylation. When we applied CESI-MS for the analysis of intact core histone subtypes from butyrate-treated mouse tumor cells, we were able to rapidly detect their degree of modification, and we found this method very useful for the separation of isobaric trimethyl and acetyl modifications. Taken together, our results highlight the need for additional techniques for the comprehensive analysis of post-translational modifications. CESI-MS is a promising new proteomics tool as demonstrated by this, the first comprehensive analysis of histone modifications, using rat testis as an example.
我们首次全面分析了源自 H1 和核心组蛋白的翻译后修饰。使用配备无鞘高灵敏度多孔喷雾器的毛细管电泳系统和纳升液相色谱电喷雾电离质谱 (nano-LC-ESI-MS) 作为两种互补技术,我们对从大鼠睾丸中分离出的 H1 组蛋白进行了分析。无需对高氯酸提取进行任何预分离,在大鼠连接组蛋白 H1.0、H1a-H1e 和 H1t 中总共鉴定出 70 种不同的修饰肽,包括 50 种磷酸肽。在 70 种修饰的 H1 组蛋白肽中,27 种肽只能通过 CESI-MS 鉴定,11 种肽只能通过 LC-ESI-MS 鉴定。MS 分析前的固定金属亲和色谱富集共得到 55 种磷酸肽;其中 22 种肽只能通过 CESI-MS 鉴定,19 种肽只能通过 LC-ESI-MS 鉴定,显示了两种技术的互补性。我们还鉴定了 42 个 H1 修饰位点,包括 31 个磷酸化位点,其中 8 个为新位点。对于核心组蛋白的分析,我们选择了不同的策略。在第一步中,硫酸提取的核心组蛋白预先通过反相高效液相色谱进行分离。以这种方式获得的各个大鼠睾丸核心组蛋白馏分被消化并通过自上而下的 CESI-MS 进行分析。这种方法鉴定了 42 个不同的修饰位点,包括乙酰化(赖氨酸和 N(α)-末端);单、二和三甲基化;和磷酸化。当我们将 CESI-MS 应用于丁酸处理的小鼠肿瘤细胞中完整的核心组蛋白亚型分析时,我们能够快速检测它们的修饰程度,并且我们发现这种方法对于分离等电的三甲基化和乙酰化修饰非常有用。总之,我们的结果强调需要额外的技术来全面分析翻译后修饰。CESI-MS 是一种很有前途的新蛋白质组学工具,正如本文首次对组蛋白修饰进行的全面分析所示,使用大鼠睾丸作为示例。