Dickhut Clarissa, Radau Sonja, Zahedi René P
Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V., Otto-Hahn-Str. 6b, 44227, Dortmund, Germany.
Methods Mol Biol. 2014;1156:417-30. doi: 10.1007/978-1-4939-0685-7_28.
Bottom-up mass spectrometry (MS) is still the method of choice for analyzing protein phosphorylation. However, the low stoichiometry of phosphorylation, especially in highly complex samples, renders the specific enrichment of phosphopeptides prior to analysis inevitable. In recent years, specific phosphopeptide enrichment strategies combined with high-performance liquid chromatography (HPLC)-MS (LC-MS) provided researchers deeper insights into the phosphorylation networks of biological systems.Here, we describe two protocols for the enrichment of phosphopeptides from biological samples using titanium dioxide (TiO2) resins, enabling the handling of small sample amounts (<20 μg of protein) as well as larger sample amounts (up to the milligram range), depending on the scientific issue to be solved.Furthermore, we imply quality control steps during sample preparation to ensure the reproducibility and reliability of the phosphoproteomic findings.
自下而上的质谱分析法(MS)仍然是分析蛋白质磷酸化的首选方法。然而,磷酸化的化学计量比很低,尤其是在高度复杂的样品中,这使得在分析之前对磷酸肽进行特异性富集成为必然。近年来,特异性磷酸肽富集策略与高效液相色谱(HPLC)-MS(LC-MS)相结合,为研究人员深入了解生物系统的磷酸化网络提供了帮助。在此,我们描述了两种使用二氧化钛(TiO2)树脂从生物样品中富集磷酸肽的方法,根据要解决的科学问题,可以处理少量样品(<20μg蛋白质)以及大量样品(高达毫克范围)。此外,我们在样品制备过程中引入了质量控制步骤,以确保磷酸化蛋白质组学研究结果的可重复性和可靠性。