Binary (Split) Light‐up Aptameric Sensors. (8th October 2020)

• Record Type: Journal Article
• Authors: Kolpashchikov, Dmitry M.; Spelkov, Alexander A.
• Is Part Of: Angewandte Chemie. Volume 133:Number 10(2021)
• Page Start: 5040
• Page End: 5051
• Publication Date: 2020-10-08
• Subjects: fluorescent protein -- in vivo imaging -- label-free sensors -- molecular beacon -- RNA nanotechnology; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201914919
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: This Minireview discusses the design and applications of binary (also known as split) light‐up aptameric sensors (BLAS). BLAS consist of two RNA or DNA strands and a fluorogenic organic dye added as a buffer component. When associated, the two strands form a dye‐binding site, followed by an increase in fluorescence of the aptamer‐bound dye. The design is cost‐efficient because it uses short oligonucleotides and does not require conjugation of organic dyes with nucleic acids. In some applications, BLAS design is preferable over monolithic sensors because of simpler assay optimization and improved selectivity. RNA‐based BLAS can be expressed in cells and used for the intracellular monitoring of biological molecules. BLAS have been used as reporters of nucleic acid association events in RNA nanotechnology and nucleic‐acid‐based molecular computation. Other applications of BLAS include the detection of nucleic acids, proteins, and cancer cells, and potentially they can be tailored to report a broad range of biological analytes. Abstract : Binary light‐up aptameric sensors (BLAS) consist of two RNA or DNA strands and a fluorogenic organic dye added as a buffer component. When associated, the two strands form a dye‐binding site, followed by an increase in fluorescence of the aptamer‐bound dye. This Minireview summarizes the state of the art in BLAS development and outlines perspectives and applications.