Spatiotemporally Controlled DNA Nanoclamps: Single-Molecule Imaging of Receptor Protein Oligomerization.
Xuan ZhaoQingzhi HanNa NaJin OuyangPublished in: Analytical chemistry (2021)
Cell membrane surface receptor proteins play an important role in cellular biological processes. There are numerous methods to detect receptors, yet developing an artificially controlled and specific detection and treatment strategy remains a challenge. Herein, we develop such a strategy based on upconversion nanoparticles (UCNPs) loaded DNA probes that enable two-color ratiometric imaging excitated by a 980 nm laser. The light response controllable signal opening strategy avoids waste during probe transportation and improves sensitivity. Thereby the number of receptors on individual DU145 cell membranes is counted by single-molecule detection. Due to the different expression of specific receptor proteins, the number of single fluorescent dots counted can be used as a basis for distinguishing DU145 from other cells. This work is highly controllable to increase sensitivity, providing a platform for cancer diagnosis and treatment.
Keyphrases
- single molecule
- living cells
- atomic force microscopy
- fluorescent probe
- high resolution
- binding protein
- quantum dots
- induced apoptosis
- label free
- photodynamic therapy
- poor prognosis
- drug delivery
- loop mediated isothermal amplification
- young adults
- high throughput
- papillary thyroid
- cell therapy
- mass spectrometry
- stem cells
- signaling pathway
- nitric oxide
- real time pcr
- cancer therapy
- energy transfer
- combination therapy
- high speed
- squamous cell
- circulating tumor cells