Aix Marseille Univ CNRS, LISM, UMR 7255, IMM FR 3479, 31 Chemin Joseph Aiguier, 13009, Marseille, France.
Institut Jean-Pierre Bourgin, INRAE, AgroParisTech, Université Paris-Saclay, 78000, Versailles, France.
Talanta. 2020 Nov 1;219:121261. doi: 10.1016/j.talanta.2020.121261. Epub 2020 Jul 2.
Guanosine tetraphosphate (G4P) and guanosine pentaphosphate (G5P) are signalling nucleotides found in bacteria and photosynthetic eukaryotes that are implicated in a wide-range of processes including stress acclimation, developmental transitions and growth control. Measurements of G4P/G5P levels are essential for studying the diverse roles of these nucleotides. However, G4P/G5P quantification is particularly challenging in plants and algae due to lower cellular concentrations, compartmentalization and high metabolic complexity. Despite recent advances the speed and accuracy of G4P quantification in plants and algae can still be improved. Here, we report a new approach for rapid and accurate G4P quantification which relies on the use of synthesized stable isotope-labelled as internal standards. We anticipate that this approach will accelerate research into the function of G4P signaling in plants, algae and other organisms.
四磷酸鸟苷 (G4P) 和五磷酸鸟苷 (G5P) 是在细菌和光合真核生物中发现的信号核苷酸,它们参与多种过程,包括应激适应、发育转变和生长控制。测量 G4P/G5P 水平对于研究这些核苷酸的多种作用至关重要。然而,由于细胞浓度较低、区室化和高代谢复杂性,在植物和藻类中定量测定 G4P/G5P 特别具有挑战性。尽管最近取得了进展,但仍可以提高植物和藻类中 G4P 定量的速度和准确性。在这里,我们报告了一种新的快速准确测定 G4P 的方法,该方法依赖于使用合成的稳定同位素标记的内标。我们预计,这种方法将加速研究 G4P 信号在植物、藻类和其他生物体中的功能。