Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Sakai 599-8531, Japan.
Curr Opin Biotechnol. 2010 Feb;21(1):35-44. doi: 10.1016/j.copbio.2010.01.012. Epub 2010 Feb 18.
Metabolomics, as an essential part of genomics studies, intends holistic understanding of metabolic networks through simultaneous analysis of a myriad of both known and unknown metabolites occurring in living organisms. The initial stage of metabolomics was designed for the reproducible analyses of known metabolites based on their comparison to available authentic compounds. Such metabolomics platforms were mostly based on mass spectrometry (MS) technologies enabled by a combination of different ionization methods together with a variety of separation steps including LC, GC, and CE. Among these, Fourier-transform ion cyclotron resonance MS (FT-ICR/MS) is distinguished from other MS technologies by its ultrahigh resolution power in mass to charge ratio (m/z). The potential of FT-ICR/MS as a distinctive metabolomics tool has been demonstrated in nontargeted metabolic profiling and functional characterization of novel genes. Here, we discuss both the advantages and difficulties encountered in the FT-ICR/MS metabolomics studies.
代谢组学作为基因组学研究的重要组成部分,旨在通过同时分析生物体内存在的大量已知和未知代谢物,全面了解代谢网络。代谢组学的初始阶段是基于对已知代谢物的可重复性分析而设计的,其基础是将其与可用的纯化合物进行比较。这些代谢组学平台大多基于质谱 (MS) 技术,该技术通过不同的电离方法与多种分离步骤(包括 LC、GC 和 CE)相结合得以实现。在这些方法中,傅里叶变换离子回旋共振质谱 (FT-ICR/MS) 因其在质荷比 (m/z) 方面的超高分辨率能力而与其他 MS 技术区分开来。FT-ICR/MS 作为一种独特的代谢组学工具的潜力已在非靶向代谢物分析和新型基因的功能表征中得到证明。在这里,我们讨论了在 FT-ICR/MS 代谢组学研究中遇到的优势和困难。