Ultrasensitive "FRET-SEF" Probe for Sensing and Imaging MicroRNAs in Living Cells Based on Gold Nanoconjugates.
Jiadi SunFuwei PiJian JiHong-Tao LeiZhixian GaoYinzhi ZhangJean de Dieu HabimanaZaijun LiXiulan SunPublished in: Analytical chemistry (2018)
MicroRNAs (miRNAs), a kind of single-stranded small RNA molecule, play significant roles in the physiological and pathological processes of human beings. Currently, miRNAs have been demonstrated as important biomarkers critically related to many diseases and life nature, including several cancers and cell senescence. It is valuable to establish sensitive assays for monitoring the levels of intracellular up-regulated/down-regulated miRNA expression, which would contribute to the early prediction of the tumor risk and cardiovascular disease. Here, an oriented gold nanocross (AuNC)-decorated gold nanorod (AuNR) probe with "OFF-enhanced ON" fluorescence switching was developed based on fluorescence resonance energy transfer and surface enhanced fluorescence (FRET-SEF) principle. The nanoprobe was used to specifically detect miRNA in vitro, which gave two linear responses represented by the equation F = 1830.32 log C + 6349.27, R2 = 0.9901, and F = 244.41 log C + 1916.10, R2 = 0.9984, respectively, along with a detection limit of 0.5 aM and 0.03 fM, respectively. Furthermore, our nanoprobe was used to dynamically monitor the expression of intracellular up-regulated miRNA-34a from the HepG2 and H9C2 cells stimulated by AFB1 and TGF-β1, and the experimental results showed that the new probe not only could be used to quantitively evaluate miRNA oncogene in vitro, but also enabled tracking and imaging of miRNAs in living cells.
Keyphrases
- living cells
- energy transfer
- quantum dots
- single molecule
- fluorescent probe
- poor prognosis
- cardiovascular disease
- endothelial cells
- transcription factor
- high resolution
- binding protein
- silver nanoparticles
- reactive oxygen species
- cell cycle arrest
- gold nanoparticles
- type diabetes
- dna damage
- transforming growth factor
- bone marrow
- coronary artery disease
- cell therapy
- single cell
- long non coding rna
- reduced graphene oxide
- cell death
- stress induced
- fluorescence imaging
- mass spectrometry
- loop mediated isothermal amplification
- molecularly imprinted
- breast cancer risk