CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging.
Xuan ZhaoNa NaJin OuyangPublished in: Chemical science (2022)
The biological state at the subcellular level is highly relevant to many diseases, and the monitoring of organelles such as mitochondria is crucial based on this. However, most DNA and protein based nanoprobes used for the detection of mitochondrial RNAs (mitomiRs) lack spatial selectivity, which leads to inefficiencies in probe delivery and signal turn-on. Herein, we constructed a novel DNA nanoprobe named protein delivery nano-corona (PDNC) to improve the delivery efficiency of Cas protein, for spatially selective imaging of mitomiRs in living cells switched on by a CRISPR/Cas system. Combined with a single-molecule counting method, this strategy enables highly sensitive detection of low-abundance mitomiR. Therefore, the strategy in this work opens up new opportunities for cell identification, early clinical diagnosis, and research in biological behaviour at the subcellular level.
Keyphrases
- single molecule
- living cells
- crispr cas
- genome editing
- sensitive detection
- atomic force microscopy
- high resolution
- fluorescent probe
- protein protein
- amino acid
- binding protein
- quantum dots
- single cell
- oxidative stress
- stem cells
- mass spectrometry
- reactive oxygen species
- small molecule
- photodynamic therapy
- endoplasmic reticulum
- cancer therapy
- mesenchymal stem cells
- cell therapy
- circulating tumor
- antibiotic resistance genes