Snyder Nathaniel W, Khezam Maya, Mesaros Clementina A, Worth Andrew, Blair Ian A
Centers for Cancer Pharmacology and Excellence in Environmental Toxicology, Department of Pharmacology, University of Pennsylvania.
J Vis Exp. 2013 May 20(75):e50433. doi: 10.3791/50433.
Here we present a workflow to analyze the metabolic profiles for biological samples of interest including; cells, serum, or tissue. The sample is first separated into polar and non-polar fractions by a liquid-liquid phase extraction, and partially purified to facilitate downstream analysis. Both aqueous (polar metabolites) and organic (non-polar metabolites) phases of the initial extraction are processed to survey a broad range of metabolites. Metabolites are separated by different liquid chromatography methods based upon their partition properties. In this method, we present microflow ultra-performance (UP)LC methods, but the protocol is scalable to higher flows and lower pressures. Introduction into the mass spectrometer can be through either general or compound optimized source conditions. Detection of a broad range of ions is carried out in full scan mode in both positive and negative mode over a broad m/z range using high resolution on a recently calibrated instrument. Label-free differential analysis is carried out on bioinformatics platforms. Applications of this approach include metabolic pathway screening, biomarker discovery, and drug development.
在此,我们展示了一种用于分析感兴趣的生物样品(包括细胞、血清或组织)代谢谱的工作流程。首先通过液 - 液萃取将样品分离为极性和非极性部分,并进行部分纯化以利于下游分析。初始萃取的水相(极性代谢物)和有机相(非极性代谢物)均进行处理,以检测广泛的代谢物。代谢物根据其分配特性通过不同的液相色谱方法进行分离。在本方法中,我们展示了微流超高效(UP)液相色谱方法,但该方案可扩展至更高流速和更低压力。进入质谱仪可通过通用或化合物优化的源条件。在最近校准的仪器上,使用高分辨率在宽质荷比范围内以正模式和负模式在全扫描模式下对广泛的离子进行检测。在生物信息学平台上进行无标记差异分析。该方法的应用包括代谢途径筛选、生物标志物发现和药物开发。