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• W2788583602 abstract "RNA aptamers that generate a strong fluorescence signal upon binding a nonfluorescent small-molecule dye offer a powerful means for the selective imaging of individual RNA species. Unfortunately, conventional in vitro discovery methods are not efficient at generating such fluorescence-enhancing aptamers, because they primarily exert selective pressure based on target affinity—a characteristic that correlates poorly with fluorescence enhancement. Thus, only a handful of fluorescence-enhancing aptamers have been reported to date. In this work, we describe a method for converting DNA libraries into “gene-linked RNA aptamer particles” (GRAPs) that each display ∼105 copies of a single RNA sequence alongside the DNA that encodes it. We then screen large libraries of GRAPs in a high-throughput manner using the FACS instrument based directly on their fluorescence-enhancing properties. Using this strategy, we demonstrate the capability to generate fluorescence-enhancing aptamers that produce a variety of different emission wavelengths upon binding the dye of interest." @default.
• W2788583602 created "2018-03-06" @default.
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• W2788583602 date "2018-03-05" @default.
• W2788583602 modified "2023-10-12" @default.
• W2788583602 title "Direct Selection of Fluorescence-Enhancing RNA Aptamers" @default.
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• W2788583602 doi "https://doi.org/10.1021/jacs.7b10724" @default.
• W2788583602 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29505267" @default.
• W2788583602 hasPublicationYear "2018" @default.
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