Trace Analysis and Biosensor Research Center, Department of Physics, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand.
J Fluoresc. 2012 Nov;22(6):1617-25. doi: 10.1007/s10895-012-1105-6. Epub 2012 Jul 19.
In order to alter a typical molecular aptamer beacon (MAB) to detect a different analyte there is currently a need to change the whole sensor unit including the expensive labeling fluorophores. In this work a DNA-based reconfigurable molecular aptamer beacon was developed. It is composed of two parts: a variable part and a constant part. The variable part comprises an aptamer strand and its complementary strand while the constant part is an oligonucleotide doubly labeled with a Förster Resonance Energy Transfer (FRET) pair and the two parts become joined via DNA hybridization. The sensor exists in two conformations: a folded (high FRET) and an unfolded (low FRET) in the absence and presence of the aptamer-target binding respectively. This sensor can be reconfigured by washing away the aptamer and the complementary strand using proper complementary strands, called washers. As a proof of the principle, a sensor that bound the enzyme thrombin, an analyte with a strong binding, was first constructed and then reconfigured to bind adenosine, selected as an analyte with a weak binding. We believe that the design is of universal use applicable to many types of aptamers.
为了将典型的分子适体荧光报告基因(MAB)改变为检测不同的分析物,目前需要改变整个传感器单元,包括昂贵的标记荧光团。在这项工作中,开发了一种基于 DNA 的可重构分子适体荧光报告基因。它由两部分组成:可变部分和恒定部分。可变部分包括适体链及其互补链,而恒定部分是用Förster 共振能量转移(FRET)对双标记的寡核苷酸,两个部分通过 DNA 杂交连接在一起。在不存在和存在适体-靶结合的情况下,传感器分别存在两种构象:折叠(高 FRET)和展开(低 FRET)。通过使用适当的互补链(称为洗涤链)洗掉适体和互补链,可以对传感器进行重新配置。作为原理的证明,首先构建了与酶凝血酶结合的传感器,凝血酶是一种具有强结合的分析物,然后将其重新配置为与腺苷结合,腺苷被选为具有弱结合的分析物。我们相信,这种设计具有普遍适用性,适用于许多类型的适体。