Visualizing orthogonal RNAs simultaneously in live mammalian cells by fluorescence lifetime imaging microscopy (FLIM).
Nadia SarfrazEmilia MoscosoTherese OertelHarrison J LeeSuman RanjitEsther BraselmannPublished in: Nature communications (2023)
Visualization of RNAs in live cells is critical to understand biology of RNA dynamics and function in the complex cellular environment. Detection of RNAs with a fluorescent marker frequently involves genetically fusing an RNA aptamer tag to the RNA of interest, which binds to small molecules that are added to live cells and have fluorescent properties. Engineering efforts aim to improve performance and add versatile features. Current efforts focus on adding multiplexing capabilities to tag and visualize multiple RNAs simultaneously in the same cell. Here, we present the fluorescence lifetime-based platform Riboglow-FLIM. Our system requires a smaller tag and has superior cell contrast when compared with intensity-based detection. Because our RNA tags are derived from a large bacterial riboswitch sequence family, the riboswitch variants add versatility for using multiple tags simultaneously. Indeed, we demonstrate visualization of two RNAs simultaneously with orthogonal lifetime-based tags.
Keyphrases
- label free
- induced apoptosis
- single molecule
- cell cycle arrest
- living cells
- high resolution
- single cell
- quantum dots
- cell therapy
- nucleic acid
- magnetic resonance
- quality improvement
- loop mediated isothermal amplification
- high throughput
- gold nanoparticles
- cell death
- dna methylation
- sensitive detection
- endoplasmic reticulum stress
- mesenchymal stem cells
- copy number
- real time pcr
- energy transfer
- mass spectrometry
- bone marrow
- high speed
- genome wide