A Modular Synthesis of Modified Phosphoanhydrides

• Published in: Chemistry : a European journal 2015-07, Vol.21 (28), p.10116-10122
• Main Authors: Hofer, Alexandre, Cremosnik, Gregor S., Müller, André C., Giambruno, Roberto, Trefzer, Claudia, Superti-Furga, Giulio, Bennett, Keiryn L., Jessen, Henning J.
• Format: Article
• Language: English
• Subjects: Anhydrides - chemical synthesis; Anhydrides - chemistry; Chemistry; chemoselectivity; Conjugates; Construction; isotopic labeling; Modular; Molecular Structure; Nucleosides; Nucleosides - chemistry; Nucleotides; Nucleotides - chemistry; Phosphates - chemical synthesis; Phosphates - chemistry; phosphorylation; polyanions; Strategy; Sugars; Synthesis
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.201500838

Phosphoanhydrides (P‐anhydrides) are ubiquitously occurring modifications in nature. Nucleotides and their conjugates, for example, are among the most important building blocks and signaling molecules in cell biology. To study and manipulate their biological functions, a diverse range of analogues have been developed. Phosphate‐modified analogues have been successfully applied to study proteins that depend on these abundant cellular building blocks, but very often both the preparation and purification of these molecules are challenging. This study discloses a general access to P‐anhydrides, including different nucleotide probes, that greatly facilitates their preparation and isolation. The convenient and scalable synthesis of, for example, 18O labeled nucleoside triphosphates holds promise for future applications in phosphoproteomics. Building the building blocks: This study discloses a general method for the functionalization of unprotected nucleotides and sugar phosphates with P‐amidites in a highly modular way. The strategy facilitates the preparation of thiophosphate‐containing nucleotides, 18O‐labeled nucleoside triphosphates, and farnesylated nucleotides, as well as a range of dinucleoside polyphosphates and nucleotide sugars.