Electrochemical Visualization of Membrane Proteins in Single Cells at a Nanoscale Using Scanning Electrochemical Cell Microscopy.
Rong JinWenting ZhouYanyan XuDe-Chen JiangDanjun FangPublished in: Analytical chemistry (2023)
The electrochemical visualization of proteins in the plasma membrane of single fixed cells was achieved with a spatial resolution of 160 nm using scanning electrochemical cell microscopy. The model protein, the carcinoembryonic antigen (CEA), is linked with a ruthenium complex (Ru(bpy) 3 2+ )-tagged antibody, which exhibits redox peaks in its cyclic voltammetry curves after a nanopipette tip contacts the cellular membrane. Based on the potential-resolved oxidation or reduction currents, an uneven distribution of membrane CEAs on the cells is electrochemically visualized, which could only be achieved previously using super-resolution optical microscopy. Compared with current electrochemical microscopy, the single-cell scanning electrochemical cell microscopy (SECCM) strategy not only improves the spatial resolution but also utilizes the potential-resolved current from the antibody-antigen complex to increase electrochemical imaging accuracy. Eventually, the electrochemical visualization of cellular proteins at the nanoscale enables the super-resolution study of cells to provide more biological information.
Keyphrases
- label free
- high resolution
- gold nanoparticles
- induced apoptosis
- single cell
- single molecule
- molecularly imprinted
- ionic liquid
- cell cycle arrest
- high throughput
- high speed
- electron microscopy
- electron transfer
- endoplasmic reticulum stress
- signaling pathway
- cell therapy
- rna seq
- healthcare
- cell death
- nitric oxide
- oxidative stress
- cell proliferation
- photodynamic therapy
- climate change
- human health
- pi k akt
- bone marrow