Reeve A E, Huang R C
Anal Biochem. 1983 Apr 1;130(1):14-8. doi: 10.1016/0003-2697(83)90643-7.
A method for the synthesis and purification of guanosine 5'-[gamma-S]triphosphate labeled with 32P in the beta-position is described. The first step in the synthesis involves the quantitative transfer of 32Pi from [gamma-32P]dATP to 5'-GMP catalyzed by GMP kinase. Further incubation of the beta-32P]GDP product with [gamma-S]GTP and nucleoside diphosphate kinase results in the synthesis of [beta-32P][gamma-S]GTP with a yield of 10 to 18%. The 32P-labeled [gamma-S]nucleotide is purified by binding to mercury-agarose and eluting with buffer containing beta-mercaptoethanol. Specific incorporation of 32P into the beta-position was demonstrated by treating [beta-32P][gamma-S]GTP with 7% formic acid to remove the gamma-thiophosphate and digesting the remaining [beta-32P]GDP with nucleotide pyro-phosphatase. Although 5'-GMP was released after pyrophosphatase digestion, the only 32P radioactivity detected was as inorganic phosphate.
描述了一种合成和纯化在β位用32P标记的鸟苷5'-[γ-S]三磷酸的方法。合成的第一步涉及由GMP激酶催化将[γ-32P]dATP中的32Pi定量转移至5'-GMP。将β-32P]GDP产物与[γ-S]GTP和核苷二磷酸激酶进一步温育,可合成[β-32P][γ-S]GTP,产率为10%至18%。通过与汞琼脂糖结合并用含β-巯基乙醇的缓冲液洗脱来纯化32P标记的[γ-S]核苷酸。用7%甲酸处理[β-32P][γ-S]GTP以去除γ-硫代磷酸酯,并用核苷酸焦磷酸酶消化剩余的[β-32P]GDP,从而证明32P特异性掺入β位。尽管焦磷酸酶消化后释放出5'-GMP,但检测到的唯一32P放射性为无机磷酸盐。