Key result
Ultrasensitive fluorescence assay achieves ~10,000-fold reporter-to-target ratio to visualize hERG channels in living cells.
A novel dual signal amplification fluorescence assay allows for ultrasensitive visualization of hERG potassium channels in living cells, offering a new tool for arrhythmia research.
Dysfunction of the human ether-a-go-go related gene (hERG)-encoded potassium channel is identified as a major cause of the long QT syndrome, a marker for lethal cardiac arrhythmia. Furthermore, recent studies revealed that hERG K + channel is a regulator of tumor cell apoptosis and proliferation. Herein, an ultrasensitive fluorescence assay combining DNA-functionalized gold nanoparticles and rolling circle amplification (RCA) was attempted for the first time to visualize hERG channels in living cells. The spherical nucleic acid gold nanoparticles, which can anchor on hERG channels in the cell membrane, not only act as the primary amplification elements but also trigger the subsequent RCA reaction to achieve the secondary amplification. Within 30 min, the ratio of reporter to target can reach up to 10 4, realizing the detection of hERG channels in cells with low-level expression. Therefore, the strategy provides a valuable tool for hERG-related studies. More importantly, it opens a new horizon for imaging various membrane proteins which possess specific aptamers or antibodies.
No takes yet. Share an insight, caveat, or question.
Yang et al. (2018) studied this question. Ultrasensitive fluorescence assay combining DNA-functionalized gold nanoparticles and rolling circle amplification (RCA) was evaluated on Visualization of hERG channels in living cells. An ultrasensitive fluorescence assay combining DNA-functionalized gold nanoparticles and rolling circle amplification achieved a reporter to target ratio of up to 10^4 within 30 minutes.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: