Lutz N W, Yahi N, Fantini J, Cozzone P J
Centre de Résonance Magnétique Biologique et Médicale, URA CNRS 1186, Faculté de Médecine, Marseille, France.
Magn Reson Med. 1996 Nov;36(5):788-95. doi: 10.1002/mrm.1910360519.
This work demonstrates that individual purine and pyrimidine NDP and NTP can be assigned in high resolution 31P NMR spectra from tissue extracts. To the best of our knowledge, it is shown for the first time that ATP, GTP, UTP, CTP, and the corresponding diphosphates can be quantitated in cell extracts without using HPLC or other biochemical methods. This work provides the basis for further optimization of nucleotide quantitation by 31P NMR spectroscopy, and for a full assessment of this method. Furthermore, a new technique was developed for 1H, 31P, and 13C NMR signal assignment and quantitation in cell extracts by using the same external reference capillary for all three nuclei. This allows for efficient, quantitative, multinuclear NMR spectroscopy without extract contamination by standard material.
这项工作表明,从组织提取物的高分辨率³¹P NMR光谱中可以明确分辨出单个嘌呤和嘧啶核苷二磷酸及核苷三磷酸。据我们所知,首次证明了无需使用高效液相色谱法或其他生化方法,就能在细胞提取物中对ATP、GTP、UTP、CTP以及相应的二磷酸进行定量分析。这项工作为通过³¹P NMR光谱进一步优化核苷酸定量分析以及全面评估该方法奠定了基础。此外,还开发了一种新技术,通过对所有三种原子核使用同一外部参比毛细管,来对细胞提取物中的¹H、³¹P和¹³C NMR信号进行归属和定量分析。这使得在不被标准物质污染提取物的情况下,能够高效、定量地进行多核磁共振光谱分析。