Probing Oxidant Effects on Superoxide Dismutase 1 Oligomeric States in Live Cells Using Single-Molecule Fluorescence Anisotropy.
Huanhuan ChenTai-Yen ChenPublished in: Chemical & biomedical imaging (2023)
The protein Cu/Zn superoxide dismutase (SOD1) is known to function as a dimer, but its concentration in cells (∼50 μM) and the dimerization constant ( K d of 500 μM) results suggest that it exists in a monomer-dimer equilibrium. It is unclear how the oligomeric state of SOD1 changes when cells are initially exposed to high levels of extracellular oxidative stress. To address this problem, we introduced the single-molecule fluorescence anisotropy (smFA) assay to explore SOD1 oligomeric states in live COS7 cells. smFA specifically probes the fluorescence polarization changes caused by molecular rotations where the fast-rotating molecules (either due to smaller hydrodynamic volume or less viscous environments) deteriorate the emission polarization and thus lower the anisotropy. After validating that smFA is effective in distinguishing monomeric and dimeric fluorescence proteins, we overexpressed SOD1 in live COS7 cells and investigated how its oligomeric state changes under basal, 2 h, and 24 h 100 μM H 2 O 2 treatments. We found that treating cells with H 2 O 2 promotes SOD1 dimerization and decreases cellular viscosity in 2 h. Interestingly, prolonged H 2 O 2 treatments show similar results as the basal conditions, indicating that cells return to a steady state similar to the basal state after 24 h, despite the presence of H 2 O 2 . Our results demonstrate that SOD1 changes its oligomeric state equilibrium in response to extracellular oxidative stresses. smFA will open new opportunities to explore the relationship between the SOD1 oligomer state and its H 2 O 2 -based signaling and transcription regulation roles.
Keyphrases
- single molecule
- induced apoptosis
- cell cycle arrest
- oxidative stress
- endoplasmic reticulum stress
- cell death
- risk assessment
- living cells
- small molecule
- mass spectrometry
- high throughput
- signaling pathway
- dna damage
- amyotrophic lateral sclerosis
- molecular dynamics
- cell proliferation
- minimally invasive
- binding protein
- pi k akt
- heavy metals
- fluorescent probe
- high speed
- fluorescence imaging