Ontology highlight
ABSTRACT: Objective
The highly conserved 14-3-3 proteins interact with key players involved in Parkinson's disease (PD) and other neurodegenerative disorders. We recently demonstrated that 14-3-3 phosphorylation is increased in PD models and that increased 14-3-3 phosphorylation reduces the neuroprotective effects of 14-3-3 proteins. Here, we investigated whether 14-3-3 phosphorylation is altered in postmortem brains from control, PD, Alzheimer's Disease (AD), Alzheimer's with Lewy Bodies (ADLB), Dementia with Lewy Bodies (DLB), and Progressive Supranuclear Palsy (PSP) subjects at three conserved sites: serine 58 (S58), serine 185 (S185), and serine 232 (S232).Methods
S58, S185, and S232 phosphorylation was measured by western blot analysis of Triton X-100 soluble and insoluble fract
SUBMITTER: McFerrin MB
PROVIDER: S-EPMC5497531 | biostudies-literature | 2017 Jul
REPOSITORIES: biostudies-literature