Markham Kelli A, Sikorski R Steven, Kohen Amnon
Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA.
Anal Biochem. 2004 Feb 1;325(1):62-7. doi: 10.1016/j.ab.2003.10.027.
A new method for the synthesis of the reduced form of beta-nicotinamide [U-14C]adenine dinucleotide 2(')-phosphate([Ad-14C]NADPH) is presented. The present synthesis results in a radioactive material with a specific activity that is greater than 220 mCi/mmol. This method could easily be adapted for syntheses of 14C-labeled NADH, NADP(+), or any nicotinamide cofactors with radiolabels in other positions. Since these cofactors are so ubiquitous, the use and applications of such labeled material has broad implications. The utility of the labeled cofactor for determination of substrates for nicotinamide-dependent enzymes in the nano- to femtomole scale, in alternative enzymatic assays, and in kinetic isotope effect studies is discussed.
本文介绍了一种合成还原型β-烟酰胺[U-14C]腺嘌呤二核苷酸2(')-磷酸([Ad-14C]NADPH)的新方法。目前的合成方法得到的放射性物质的比活度大于220 mCi/mmol。该方法可轻松适用于14C标记的NADH、NADP(+)或其他位置带有放射性标记的任何烟酰胺辅因子的合成。由于这些辅因子非常普遍,此类标记物质的使用和应用具有广泛的意义。本文还讨论了标记辅因子在纳摩尔至飞摩尔规模下用于测定烟酰胺依赖性酶的底物、替代酶促测定以及动力学同位素效应研究中的效用。