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Tyrosine 133 mutation does not alter the accumulation of reactive oxygen and nitrogen species.
Abstract
<p>(A, B) Quantification of cells expressing different αSyn variants displaying ROS and RNS assessed with flow cytometry analysis. αSyn expression was induced for 6 h and the cells were stained for 1.5 h with DHR123 to visualize ROS (A) or with DAF-2 DA to visualize RNS (B). Forward scatter (FSC) and DHR123 (A) or DAF-2 DA (B) fluorescence of the cells, showing one representative result from at least four independent experiments. The percentage of the sub-populations of yeast cells with higher fluorescent intensities (P1) than the background are presented in the lower panels. Significance of differences was calculated with one-way ANOVA (****, <i>p</i> < 0.0001).</p- Image
- Figure
- Biophysics
- Biochemistry
- Cell Biology
- Plant Biology
- Computational Biology
- Environmental Sciences not elsewhere classified
- Biological Sciences not elsewhere classified
- yeast flavohemoglobin gene YHB 1
- C-terminal Y 133
- C-terminal tyrosine modifications
- wild-type α Syn
- C-terminal tyrosine nitration increases pathogenicity
- S 129-independent proteasome clearance
- PD
- 30P α Syn
- 30P mitochondrial fragmentation
- C-Terminal Tyrosine Residue Modifications Modulate
- α Syn
- α Syn cytotoxicity
- α Syn di-tyrosine dimers
- S 129 phosphorylation
- Lewy bodies
- peroxynitrite-induced nitrative stress
- Nitrated tyrosine residues
- tyrosine residues
- α Syn inclusion formation