Kikuchi Nanami, Kolpashchikov Dmitry M
Chemistry Department, University of Central Florida, 4000 Central Florida Boulevard, Orlando, FL, 32816-2366, USA.
Chembiochem. 2016 Sep 2;17(17):1589-92. doi: 10.1002/cbic.201600323. Epub 2016 Jul 15.
Split spinach aptamer (SSA) probes for fluorescent analysis of nucleic acids were designed and tested. In SSA design, two RNA or RNA/DNA strands hybridized to a specific nucleic acid analyte and formed a binding site for low-fluorescent 3,5-difluoro-4-hydroxybenzylidene imidazolinone (DFHBI) dye, which resulted in up to a 270-fold increase in fluorescence. The major advantage of the SSA over state-of-the art fluorescent probes is high selectivity: it produces only background fluorescence in the presence of a single-base-mismatched analyte, even at room temperature. SSA is therefore a promising tool for label-free analysis of nucleic acids at ambient temperatures.
设计并测试了用于核酸荧光分析的分裂菠菜适配体(SSA)探针。在SSA设计中,两条RNA或RNA/DNA链与特定的核酸分析物杂交,并形成一个低荧光3,5-二氟-4-羟基苄叉咪唑啉酮(DFHBI)染料的结合位点,这导致荧光增强高达270倍。与现有技术的荧光探针相比,SSA的主要优点是选择性高:即使在室温下,在存在单碱基错配分析物的情况下,它也只会产生背景荧光。因此,SSA是一种在环境温度下进行核酸无标记分析的有前途的工具。