Department of Chemistry, College of Natural Sciences, Seoul National University, Seoul 151-747, Korea.
J Org Chem. 2011 Jan 21;76(2):417-23. doi: 10.1021/jo1017102. Epub 2010 Dec 21.
Among the numerous chemosensors available for diphosphate (P(2)O(7)(4-), PPi) and nucleoside triphosphates (NTPs), only a few can distinguish between PPi and NTPs. Hence, very few bioanalytical applications based on such selective chemosensors have been realized. We have developed a new fluorescence sensing system for distinction between PPi and NTPs based on the combination of two sensors, a binuclear Zn(II) complex (1·2Zn) and boronic acid (BA), in which one chemosensor (1·2Zn) shows signal changes depending on the PPi (or NTP) concentration, and the other (BA) blocks the signal change caused by NTPs; this system enables the distinction of PPi from NTPs and is sensitive to nanomolar concentrations of PPi. The new sensing system has been successfully used for the direct quantification of RNA polymerase activity.
在众多可用于二磷酸(P(2)O(7)(4-), PPi)和核苷三磷酸(NTPs)的化学传感器中,只有少数几种能够区分 PPi 和 NTPs。因此,基于此类选择性化学传感器的生物分析应用很少得到实现。我们开发了一种新的荧光传感系统,用于区分 PPi 和 NTPs,该系统基于两个传感器的组合,即双核 Zn(II)配合物(1·2Zn)和硼酸(BA),其中一个化学传感器(1·2Zn)根据 PPi(或 NTP)浓度显示信号变化,而另一个(BA)则阻止 NTP 引起的信号变化;该系统能够区分 PPi 和 NTPs,并且对纳摩尔浓度的 PPi 敏感。该新传感系统已成功用于直接定量 RNA 聚合酶活性。