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
- single cell
- living cells
- quantum dots
- cell therapy
- nucleic acid
- endoplasmic reticulum stress
- quality improvement
- magnetic resonance
- gold nanoparticles
- signaling pathway
- loop mediated isothermal amplification
- oxidative stress
- optical coherence tomography
- sensitive detection
- cell death
- mesenchymal stem cells
- energy transfer
- cell proliferation
- computed tomography
- mass spectrometry
- dna methylation
- amino acid
- high speed
- contrast enhanced
- pi k akt