TR&D 1 Isobaric Mass Tags for Ultra-Plexed Protein Quantification p. 398

项目摘要 蛋白质定量技术的持续发展是现代生物学和医学的关键。 实际上，在定量分析（多重）期间平行处理样品的能力对于许多生物技术领域是必不可少的。 DBP的应用。通过化学标记的样品多路复用提供了许多关键优势。第一、 在单个质谱分析中并行处理样品减少了所需的材料量 从任何一个样本;这是特别相关的组织为基础的工作。其次，多路复用大大减少了 样品制备和仪器分析时间要求，这对于扩展应用至关重要 蛋白质组学分析到转化医学。第三，高度复杂的分析有助于收集生物信息。 复制数据，这显然是该领域进步的必要条件。第四，能够将联合收割机样品组合成 单次分析允许更少的MS实验，这反过来又允许在所有条件下更大的数据重叠。 最后，化学标记与生物组织和液体相容。我们得出结论， 生物液体和组织对于蛋白质组学在转化医学中的应用至关重要。在这个TR & D 我们的目标是将化学标记扩展到前所未有的30重分析，并有可能进行更多的分析。 更高，通过合成新的中子编码的化学标签。此外，我们将开发新技术， MS/MS采样重叠，因为需要进行MS/MS扫描和鉴定，以从 等压标记

Project Summary The continued development of protein quantification technologies is key to modern biology and medicine. Indeed, the ability to parallel process samples during quantitative analysis (multiplex) is essential for many of the proposed DBP applications. Sample multiplexing via chemical labeling offers numerous key advantages. First, parallel processing of samples in a single mass spectrometric analysis reduces the amount of material required from any one sample; this is particularly relevant for tissue-based work. Second, multiplexing greatly reduces sample preparation and instrument analysis time requirements, which is essential for the expanded application of proteomic analysis to translational medicine. Third, highly plexed analyses facilitate collection of biological replicate data, an obvious requisite for the field's advancement. Fourth, the ability to combine samples into a single analysis permits fewer MS experiments, which in turn allows for greater data overlap across all conditions. Finally, chemical labeling is compatible with biological tissues and fluids. We conclude the ability to analyze biological fluids and tissues is vital for the application of proteomics to translational medicine. In this TR&D project we aim to expand chemical labeling to an unprecedented 30-plex analysis, with the possibility to go much higher, by synthesis of new neutron-encoded chemical tags. Further, we will develop new technologies to boost MS/MS sampling overlap, since an MS/MS scan and identification is required to obtain quantitative data from isobaric tagging.