The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization
National Institute on Aging · Brandeis University
Abstract
Loss-of-function DJ-1 mutations can cause early-onset Parkinson's disease. The function of DJ-1 is unknown, but an acidic isoform accumulates after oxidative stress, leading to the suggestion that DJ-1 is protective under these conditions. We addressed whether this represents a posttranslational modification at cysteine residues by systematically mutating cysteine residues in human DJ-1. WT or C53A DJ-1 was readily oxidized in cultured cells, generating a pI 5.8 isoform, but an artificial C106A mutant was not. We observed a cysteine-sulfinic acid at C106 in crystalline DJ-1 but no modification of C53 or C46. Oxidation of DJ-1 was promoted by the crystallization procedure. In addition, oxidation-induced…
Citation impact
- FWCI
- 37.83
- Percentile
- 100%
- References
- 33
Authors
10- RCRosa Canet-AvilesCorresponding
National Institute on Aging, Brandeis University
- MAMark A. Wilson
National Institute on Aging, Brandeis University
- DWDavid W. Miller
National Institute on Aging, Brandeis University
- RARili Ahmad
National Institute on Aging, Brandeis University
- CMChris McLendon
National Institute on Aging, Brandeis University
Topics & keywords
- Cysteine
- Neuroprotection
- Gene isoform
- Oxidative stress
- Mitochondrion
- Biochemistry
- Mutant
- Chemistry
- Good health and well-being