Near-Infrared Small Molecule as a Specific Fluorescent Probe for Ultrasensitive Recognition of Antiparallel Human Telomere G-Quadruplexes.
Ming JinJing LiYang ChenJie ZhaoJiahui ZhangZhen ZhangPeiyao DuLibing ZhangXiao-Quan LuPublished in: ACS applied materials & interfaces (2021)
In the past 10 years, many fluorescent probes have been developed to recognize G-quadruplexes (G4s) since G4s play an important role in biological systems. However, the selectivity and sensitivity of existing probes for G4s limit their further applications. Herein, we design and synthesize a new probe (TOVJ) by introducing 9-vinyljulolidine into TO. The new probe exhibits almost no fluorescence in an aqueous solution. Upon interacting with G4s, especially the antiparallel G4s, the fluorescence intensity was greatly enhanced (maximum 2742-fold) with a large Stokes shift of 198 nm and the maximum emission peak at 694 nm (near-infrared region). TOVJ showed high sensitivity and selectivity to G4s over other DNA topologies (ssDNA/dsDNA), especially to antiparallel G4s. For antiparallel human telomere G4 detection, the limits of detection of Hum24 and 22AG Na+ were as low as 164 and 231 pM, respectively. This indicates that TOVJ is a highly sensitive fluorescence sensor that can be effectively used for antiparallel human telomere G4 detection. The result of live-cell imaging showed that TOVJ could enter live cells and locate in the mitochondria.
Keyphrases
- living cells
- fluorescent probe
- single molecule
- small molecule
- endothelial cells
- quantum dots
- label free
- pluripotent stem cells
- induced pluripotent stem cells
- loop mediated isothermal amplification
- induced apoptosis
- photodynamic therapy
- fluorescence imaging
- high resolution
- real time pcr
- energy transfer
- mass spectrometry
- heavy metals
- risk assessment
- cell cycle arrest
- protein protein
- highly efficient
- molecularly imprinted