Sparano Brian A, Koide Kazunori
Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, USA.
J Am Chem Soc. 2007 Apr 18;129(15):4785-94. doi: 10.1021/ja070111z. Epub 2007 Mar 27.
Here, we describe a new paradigm for the development of small molecule-based RNA sensors. We prepared a series of potential PET (photoinduced electron transfer) sensors on the basis of 2',7'-dichlorofluorescein (DCF) fluorophore conjugated with two aniline derivatives as electron donors (quenchers). NMR and fluorescent spectroscopic analyses of these DCF derivatives revealed the correlation between the conformations, the PET, and the fluorescent intensities of these DCF derivatives, enabling us to select a sensor candidate. RNA aptamers were raised against the aniline-based quencher via in vitro selection (SELEX). One of these aptamers enhanced the fluorescence intensity of the DCF-aniline conjugate in a concentration-dependent manner. To demonstrate the power and generality of this approach, additional in vitro selection was performed and aptamers from this selection were found to have similar activities. These results show that one can develop fluorescence-inducing reporter RNA and morph it into remotely related sequences without prior structural insight into RNA-ligand binding.
在此,我们描述了一种基于小分子的RNA传感器开发的新范式。我们基于与两种苯胺衍生物(作为电子供体(猝灭剂))共轭的2',7'-二氯荧光素(DCF)荧光团制备了一系列潜在的PET(光诱导电子转移)传感器。对这些DCF衍生物的NMR和荧光光谱分析揭示了这些DCF衍生物的构象、PET和荧光强度之间的相关性,使我们能够选择一种传感器候选物。通过体外筛选(SELEX)产生了针对基于苯胺的猝灭剂的RNA适配体。其中一种适配体以浓度依赖的方式增强了DCF-苯胺共轭物的荧光强度。为了证明这种方法的有效性和通用性,进行了额外的体外筛选,发现来自该筛选的适配体具有相似的活性。这些结果表明,人们可以开发出诱导荧光的报告RNA,并将其转化为远距离相关的序列,而无需事先对RNA-配体结合进行结构洞察。