Construction of a Quantum-Dot-Based FRET Nanosensor through Direct Encoding of Streptavidin-Binding RNA Aptamers for N6-Methyladenosine Demethylase Detection.
Qian ZhangShuangnan ZhaoCong SuQian HanYun HanXiaorui TianYueying LiShuangshuang ZhangPublished in: Analytical chemistry (2023)
N6-Methyladenosine (m 6 A) demethylases can catalyze the removal of the methyl modification on m 6 A, and it is closely associated with the occurrence, proliferation, differentiation, and metastasis of malignancies. The m 6 A demethylases (e.g., fat mass and obesity-associated protein (FTO)) may act as a cancer biomarker and are crucial for anticancer drug screening and early clinical diagnosis. Herein, we demonstrate the construction of a quantum-dot-based Förster resonance energy-transfer (FRET) nanosensor through direct encoding of streptavidin-binding RNA aptamers (SA aptamers) for m 6 A demethylase detection. This nanosensor employs multiple Cy5-molecule-labeled SA aptamers as the building materials to construct the 605QD-RNA-Cy5 nanoassembly, and it exploits the hinder effect of m 6 A upon elongation and ligation reactions to distinguish m 6 A-containing RNA probes from demethylated RNA probes. When m 6 A demethylase is present, the m 6 A-containing RNA probes are demethylated to generate the demethylated RNA probes, initiating strand extension and ligation reactions to yield a complete transcription template for SA aptamers. Subsequently, a T7-assisted cascade transcription amplification reaction is activated to transcribe abundant SA aptamers with the incorporation of multiple Cy5 fluorophores. The Cy5-incorporated SA aptamers can self-assembly onto the streptavidin-coated 605QD surface to obtain the 605QD-SA aptamer-Cy5 nanoassemblies, resulting in the generation of distinct FRET signals. This nanosensor exhibits ultrahigh sensitivity and excellent specificity, and it can detect endogenous FTO at the single-cell level. Furthermore, this nanosensor can precisely measure enzyme kinetic parameters, screen m 6 A demethylase inhibitors, and differentiate the FTO expression between breast cancer patients and healthy individual tissues, offering a versatile platform for clinical diagnostic and drug discovery.
Keyphrases
- nucleic acid
- energy transfer
- single molecule
- living cells
- quantum dots
- type diabetes
- small molecule
- drug discovery
- metabolic syndrome
- gene expression
- transcription factor
- label free
- fluorescent probe
- insulin resistance
- poor prognosis
- risk assessment
- signaling pathway
- mass spectrometry
- skeletal muscle
- young adults
- physical activity
- real time pcr
- photodynamic therapy
- weight gain
- electronic health record
- high resolution
- rna seq
- molecularly imprinted