Center for Systems Microbiology, Department of Systems Biology, Technical University of Denmark, Lyngby, Denmark.
Anal Biochem. 2011 Feb 15;409(2):249-59. doi: 10.1016/j.ab.2010.10.029. Epub 2010 Oct 29.
Quantification of nucleotides is an important part of metabolomics but has been hampered by the lack of fast, sensitive, and reliable methods. We present a less time-consuming, more sensitive, and more precise method for the quantitative determination of nucleoside triphosphates (NTPs), 5-ribosyl-1-pyrophosphate (PRPP), and inorganic pyrophosphate (PP(i)) in cell extracts. The method uses one-dimensional thin-layer chromatography (TLC) and radiolabeled biological samples. Nucleotides are resolved at the level of ionic charge in an optimized acidic ammonium formate and chloride solvent, permitting quantification of NTPs. The method is significantly simpler and faster than both current two-dimensional methods and high-performance liquid chromatography (HPLC)-based procedures, allowing a higher throughput while common sources of inaccuracies and technical problems are avoided. For determination of PP(i), treatment with inorganic pyrophosphatase (PPase) of the radiolabeled phosphate is employed for removal of contaminating pyrophosphate. Biological examples performed in triplicates showed standard deviations of approximately 10% of the mean for the determined concentrations of NTPs.
核苷酸的定量分析是代谢组学的重要组成部分,但由于缺乏快速、灵敏和可靠的方法而受到阻碍。我们提出了一种耗时更短、更灵敏、更精确的方法,用于定量测定核苷三磷酸(NTPs)、5-核糖-1-焦磷酸(PRPP)和无机焦磷酸(PP(i))在细胞提取物中的含量。该方法使用一维薄层层析(TLC)和放射性标记的生物样本。核苷酸在优化的酸性甲酸铵和氯化溶剂中根据离子电荷水平进行分离,从而能够定量测定 NTPs。该方法比目前的二维方法和基于高效液相色谱(HPLC)的方法都更加简单和快速,在提高通量的同时避免了常见的不准确和技术问题来源。对于 PP(i)的测定,使用无机焦磷酸酶(PPase)处理放射性标记的磷酸盐以去除杂质焦磷酸盐。重复进行了三次的生物学实例显示,所测定的 NTP 浓度的标准偏差约为平均值的 10%。