Accurate analysis of microRNAs (miRNAs) at the single-cell level is extremely important for deeply understanding their multiple and intricate biological functions. Despite some advancements in analyzing single-cell miRNAs, challenges such as intracellular interferences and insufficient detection limits still remain. In this work, an ultrasensitive nanopore sensor for quantitative single-cell miRNA-155 detection is constructed based on ionic current rectification (ICR) coupled with enzyme-free catalytic hairpin assembly (CHA). Benefiting from the enzyme-free CHA amplification strategy, the detection limit of the nanopore sensor for miRNA-155 reaches 10 fM and the nanopore sensor is more adaptable to complex intracellular environments. With the nanopore sensor, the concentration of miRNA-155 in living single cells is quantified to realize the early diagnosis of triple-negative breast cancer (TNBC). Furthermore, the nanopore sensor can be applied in screening anticancer drugs by tracking the expression level of miRNA-155. This work provides an adaptive and universal method for quantitatively analyzing intracellular miRNAs, which will greatly improve our understanding of cell heterogeneity and provide a more reliable scientific basis for exploring major diseases at the single-cell level.
Keyphrases
- single cell
- single molecule
- solid state
- rna seq
- high throughput
- label free
- loop mediated isothermal amplification
- poor prognosis
- real time pcr
- reactive oxygen species
- ionic liquid
- induced apoptosis
- gold nanoparticles
- high resolution
- stem cells
- wastewater treatment
- cell proliferation
- oxidative stress
- mesenchymal stem cells
- cell death
- bone marrow
- signaling pathway
- mass spectrometry
- binding protein
- simultaneous determination
- cell cycle arrest
- tandem mass spectrometry