ISOTOPE-ASSISTED DIFFERENTIAL METABOLOMICS

同位素辅助差异代谢组学

• 批准号: 8168939
• 负责人: JOHN LUTE MARKLEY
• 金额: $ 2.36万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-03-01 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8168939
• 关键词: Arabidopsis; Biological; Cataloging; Catalogs; Chemicals; Computer Retrieval of Information on Scientific Projects Database; Coupled; Databases; Funding; Future; Grant; Institution; Isotopes; Mass Spectrum Analysis; Monitor; NMR Spectroscopy; One-Step dentin bonding system; Research; Research Personnel; Resources; Sampling; Source; Stable Isotope Labeling; Structure; Technology; Time; United States National Institutes of Health; high throughput analysis; human tissue; metabolomics; novel strategies; small molecule

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Obtain additional spectral information from representatives of the 100 important metabolites of Arabidopsis and populate the database. In the future, we will have a catalog containing the structures of the 10,000 or more' most-abundant small molecules in all human tissues. We will also be able to use this information to monitor their fluctuations in concentration in real time, as our bodies continually change. The purpose of this proposal is to take us one step closer to creating metabolomic technologies to fill this void. This proposal explores the use of stable isotope labeling of biological samples coupled with the analytical high sensitivity of mass spectrometry (MS) and the chemical selectivity of high-field NMR spectroscopy as enabling technologies for high-throughput analysis of metabolomes. We call this novel approach isotope assisted metabolomics.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 从拟南芥的100种重要代谢物的代表中获得额外的光谱信息并填充数据库。在未来，我们将拥有一个包含所有人体组织中10，000或更多“最丰富的小分子”结构的目录。我们还将能够利用这些信息来监测它们在真实的时间内的浓度波动，因为我们的身体在不断变化。这项提议的目的是让我们更接近创造代谢组学技术来填补这一空白。该提案探讨了使用稳定同位素标记的生物样品加上分析的高灵敏度的质谱（MS）和化学选择性的高场NMR光谱作为使能技术的代谢组的高通量分析。我们称这种新方法为同位素辅助代谢组学。