A Family of "Click" Nucleosides for Metal-Mediated Base Pairing: Unravelling the Principles of Highly Stabilizing Metal-Mediated Base Pairs

作者：Richters Tim; Krug Olga; Koesters Jutta; Hepp Alexander; Mueller Jens

来源：Chemistry - A European Journal, 2014, 20(25): 7811-7818.

DOI：10.1002/chem.201402221

• bioinorganic chemistry
• click chemistry
• cycloaddition
• DNA
• silver

A family of artificial nucleosides has been developed by applying the Cu-I-catalyzed Huisgen 1,3-dipolar cycloaddition. Starting from 2-deoxy-beta-D-glycosyl azide as a common precursor, three bidentate nucleosides have been synthesized. The 1,2,3-triazole involved in all three nucleobases is complemented by 1,2,4-triazole (TriTri), pyrazole (TriPyr), or pyridine (TriPy). Molecular structures of two metal complexes indicate that metal-mediated base pairs of TriPyr may not be fully planar. An investigation of DNA oligonucleotide duplexes comprising the new "click" nucleosides showed that they can bind Ag-I to form metal-mediated base pairs. In particular the mispair formed from TriPy and the previously established imidazole nucleoside is significantly stabilized in the presence of Ag-I. A comparison of different oligonucleotide sequences allowed the determination of general factors involved in the stabilization of nucleic acids duplexes with metal-mediated base pairs.

• 出版日期2014-6-16