Weindl Daniel, Wegner André, Hiller Karsten
Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-Belval, Luxembourg.
Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-Belval, Luxembourg.
Methods Enzymol. 2015;561:277-302. doi: 10.1016/bs.mie.2015.04.003. Epub 2015 Jun 14.
Stable isotopes have been used to trace atoms through metabolism and quantify metabolic fluxes for several decades. Only recently non-targeted stable isotope labeling approaches have emerged as a powerful tool to gain insights into metabolism. However, the manual detection of isotopic enrichment for a non-targeted analysis is tedious and time consuming. To overcome this limitation, the non-targeted tracer fate detection (NTFD) algorithm for the automated metabolome-wide detection of isotopic enrichment has been developed. NTFD detects and quantifies isotopic enrichment in the form of mass isotopomer distributions (MIDs) in an automated manner, providing the means to trace functional groups, determine MIDs for metabolic flux analysis, or detect tracer-derived molecules in general. Here, we describe the algorithmic background of NTFD, discuss practical considerations for the freely available NTFD software package, and present potential applications of non-targeted stable isotope labeling analysis.
几十年来,稳定同位素一直被用于追踪原子在代谢过程中的踪迹并量化代谢通量。直到最近,非靶向稳定同位素标记方法才作为一种深入了解代谢的强大工具出现。然而,手动检测非靶向分析中的同位素富集既繁琐又耗时。为克服这一限制,已开发出用于自动全代谢组范围检测同位素富集的非靶向示踪剂命运检测(NTFD)算法。NTFD以质量同位素异构体分布(MIDs)的形式自动检测和量化同位素富集,提供追踪官能团、确定用于代谢通量分析的MIDs或一般检测示踪剂衍生分子的方法。在此,我们描述NTFD的算法背景,讨论免费提供的NTFD软件包的实际注意事项,并介绍非靶向稳定同位素标记分析的潜在应用。