Justesen J, Ferbus D, Thang M N
Nucleic Acids Res. 1980 Jul 25;8(14):3073-85. doi: 10.1093/nar/8.14.3073.
The interferon induced enzyme 2'5' oligoadenylate synthetase produces 2'5' pppA(pA)n the first discovered natural nucleotide with a 2'5' linkage. We describe a direct assay of this enzyme based on separation by thin layer chromatography (TLC) of the substrate ATP and the products 2'5' pppA(pA)n (n larger than or equal to 1). This technique presents obvious advantages compared to the currently used methods. Moreover the enzyme uses other nucleotides as substrates forming co-oligonucleotides 2'5 pppA(pA)n pN (N = U,G,C,dA,dG,dT and dC). Additional procedures are described using different developing solvent systems for the separation of the core-2'5' oligonucleotides (2'5' A(pA)npN) containing AMP-residues entirely and those with another nucleotide at the 2' end.
干扰素诱导酶2'5'寡腺苷酸合成酶产生2'5' pppA(pA)n,这是首次发现的具有2'5'连接的天然核苷酸。我们描述了一种基于薄层色谱(TLC)分离底物ATP和产物2'5' pppA(pA)n(n大于或等于1)的该酶直接检测方法。与目前使用的方法相比,该技术具有明显优势。此外,该酶使用其他核苷酸作为底物形成共寡核苷酸2'5 pppA(pA)n pN(N = U、G、C、dA、dG、dT和dC)。还描述了使用不同展开溶剂系统分离完全含有AMP残基的核心2'5'寡核苷酸(2'5' A(pA)npN)和2'端带有另一种核苷酸的寡核苷酸的其他方法。