Ji Debin, Mohsen Michael G, Harcourt Emily M, Kool Eric T
Department of Chemistry, Stanford University, Stanford, CA, 94305, USA.
Angew Chem Int Ed Engl. 2016 Feb 5;55(6):2087-91. doi: 10.1002/anie.201509131. Epub 2016 Jan 6.
A new strategy is reported for the production of luminescence signals from DNA synthesis through the use of chimeric nucleoside tetraphosphate dimers in which ATP, rather than pyrophosphate, is the leaving group. ATP-releasing nucleotides (ARNs) were synthesized as derivatives of the four canonical nucleotides. All four derivatives are good substrates for DNA polymerase, with Km values averaging 13-fold higher than those of natural dNTPs, and kcat values within 1.5-fold of those of native nucleotides. Importantly, ARNs were found to yield very little background signal with luciferase. DNA synthesis experiments show that the ATP byproduct can be harnessed to elicit a chemiluminescence signal in the presence of luciferase. When using a polymerase together with the chimeric nucleotides, target DNAs/RNAs trigger the release of stoichiometrically large quantities of ATP, thereby allowing sensitive isothermal luminescence detection of nucleic acids as diverse as phage DNAs and short miRNAs.
据报道,一种新策略可通过使用嵌合核苷四磷酸二聚体从DNA合成中产生发光信号,其中ATP而非焦磷酸作为离去基团。ATP释放核苷酸(ARN)被合成为四种标准核苷酸的衍生物。所有四种衍生物都是DNA聚合酶的良好底物,其Km值平均比天然dNTPs高13倍,kcat值在天然核苷酸的1.5倍以内。重要的是,发现ARN与荧光素酶产生的背景信号非常少。DNA合成实验表明,在荧光素酶存在的情况下,ATP副产物可用于引发化学发光信号。当将聚合酶与嵌合核苷酸一起使用时,靶DNA/RNA会触发化学计量的大量ATP释放,从而能够对噬菌体DNA和短miRNA等多种核酸进行灵敏的等温发光检测。