Chokkathukalam Achuthanunni, Kim Dong-Hyun, Barrett Michael P, Breitling Rainer, Creek Darren J
Glasgow Polyomics, Wolfson Wohl Cancer Research Centre, College of Medical Veterinary & Life Sciences, University of Glasgow, G61 1QH, UK.
Bioanalysis. 2014 Feb;6(4):511-24. doi: 10.4155/bio.13.348.
The rapid emergence of metabolomics has enabled system-wide measurements of metabolites in various organisms. However, advances in the mechanistic understanding of metabolic networks remain limited, as most metabolomics studies cannot routinely provide accurate metabolite identification, absolute quantification and flux measurement. Stable isotope labeling offers opportunities to overcome these limitations. Here we describe some current approaches to stable isotope-labeled metabolomics and provide examples of the significant impact that these studies have had on our understanding of cellular metabolism. Furthermore, we discuss recently developed software solutions for the analysis of stable isotope-labeled metabolomics data and propose the bioinformatics solutions that will pave the way for the broader application and optimal interpretation of system-scale labeling studies in metabolomics.
代谢组学的迅速兴起使得在各种生物体中对代谢物进行全系统测量成为可能。然而,对代谢网络的机制理解进展仍然有限,因为大多数代谢组学研究无法常规地提供准确的代谢物鉴定、绝对定量和通量测量。稳定同位素标记为克服这些限制提供了机会。在这里,我们描述了一些当前稳定同位素标记代谢组学的方法,并举例说明了这些研究对我们理解细胞代谢所产生的重大影响。此外,我们讨论了最近开发的用于分析稳定同位素标记代谢组学数据的软件解决方案,并提出了生物信息学解决方案,这些方案将为代谢组学中系统规模标记研究的更广泛应用和最佳解读铺平道路。