Tam-Chang Suk-Wah, Carson Travis D, Huang Liming, Publicover Nelson G, Hunter Kenneth W
Department of Chemistry, College of Science, University of Nevada, Reno, NV 89557, USA.
Anal Biochem. 2007 Jul 15;366(2):126-30. doi: 10.1016/j.ab.2007.03.006. Epub 2007 Mar 13.
In this article, we present the design principles and application of a motif composed of a stem-loop probe (SP) hybridized to a fluorescently labeled universal reporter (UR) for sensing unlabeled nucleic acids. At room temperature, SP-UR is in the hairpin-closed form in which the fluorophore of UR is in proximity to the G bases of the hairpin, where consequently the fluorescent emission is quenched significantly. On hybridization with target, SP-UR is trapped in the hairpin-opened configuration in which the fluorophore and the G quenchers are apart. This turns off quenching, increases emission intensity, and signals the presence of target. Compared with the common approach that employs an oligonucleotide probe with a covalently linked fluorophore, the use of a fluorescently labeled universal reporter strand hybridized to an unlabeled stem-loop probe provides a more efficient approach to the fabrication of nucleic acid sensors and microarrays potentially useful for real-time analysis.
在本文中,我们介绍了一种由茎环探针(SP)与荧光标记通用报告分子(UR)杂交组成的基序的设计原理及应用,用于检测未标记的核酸。在室温下,SP-UR呈发夹封闭形式,其中UR的荧光团靠近发夹的G碱基,因此荧光发射被显著淬灭。与靶标杂交时,SP-UR被困在发夹打开的构型中,此时荧光团和G淬灭剂分离。这消除了淬灭,增加了发射强度,并表明靶标的存在。与使用共价连接荧光团的寡核苷酸探针的常用方法相比,使用与未标记茎环探针杂交的荧光标记通用报告链为制造可能用于实时分析的核酸传感器和微阵列提供了一种更有效的方法。