6 research outputs found
Development and Applications of Fluorogen/Light-Up RNA Aptamer Pairs for RNA Detection and More.
The central role of RNA in living systems made it highly desirable to have noninvasive and sensitive technologies allowing for imaging the synthesis and the location of these molecules in living cells. This need motivated the development of small pro-fluorescent molecules called "fluorogens" that become fluorescent upon binding to genetically encodable RNAs called "light-up aptamers." Yet, the development of these fluorogen/light-up RNA pairs is a long and thorough process starting with the careful design of the fluorogen and pursued by the selection of a specific and efficient synthetic aptamer. This chapter summarizes the main design and the selection strategies used up to now prior to introducing the main pairs. Then, the vast application potential of these molecules for live-cell RNA imaging and other applications is presented and discussed.journal article2020importe
Genetically Encoded Catalytic Hairpin Assembly for Sensitive RNA Imaging in Live Cells
DNA
and RNA nanotechnology has been used for the development of
dynamic molecular devices. In particular, programmable enzyme-free
nucleic acid circuits, such as catalytic hairpin assembly, have been
demonstrated as useful tools for bioanalysis and to scale up system
complexity to an extent beyond current cellular genetic circuits.
However, the intracellular functions of most synthetic nucleic acid
circuits have been hindered by challenges in the biological delivery
and degradation. On the other hand, genetically encoded and transcribed
RNA circuits emerge as alternative powerful tools for long-term embedded
cellular analysis and regulation. Herein, we reported a genetically
encoded RNA-based catalytic hairpin assembly circuit for sensitive
RNA imaging inside living cells. The split version of Broccoli, a
fluorogenic RNA aptamer, was used as the reporter. One target RNA
can catalytically trigger the fluorescence from tens-to-hundreds of
Broccoli. As a result, target RNAs can be sensitively detected. We
have further engineered our circuit to allow easy programming to image
various target RNA sequences. This design principle opens the arena
for developing a large variety of genetically encoded RNA circuits
for cellular applications