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Redox proteomics identification of 4‐hydroxynonenal‐modified brain proteins in Alzheimer's disease: Role of lipid peroxidation in Alzheimer's disease pathogenesis
Authors:Marzia Perluigi  Rukhsana Sultana  Giovanna Cenini  Fabio Di Domenico  Maurizio Memo  William M Pierce  Raffaella Coccia  D Allan Butterfield
Affiliation:1. Department of Biochemical Sciences, University of Rome “La Sapienza”, Rome, Italy;2. Both authors contributed equally to this work.;3. Department of Chemistry, University of Kentucky, Lexington, KY, USA;4. Department of Biomedical Sciences and Biotechnologies, University of Brescia, Brescia, Italy;5. Department of Pharmacology, University of Louisville School of Medicine and VAMC, Louisville, KY, USA;6. Center of Membrane Sciences, University of Kentucky, Lexington, KY, USA;7. Sanders‐Brown Center on Aging, University of Kentucky, Lexington, KY, USA
Abstract:Numerous studies have shown that neuronal lipids are highly susceptible to oxidative stress including in those brain areas directly involved in the neurodegenerative process of Alzheimer's disease (AD). Lipid peroxidation directly damages membranes and also generates a number of secondary biologically active products (toxic aldehydes)that are capable of easily attacking lipids, proteins, and DNA. Accumulating evidence has demonstrated regionally increased brain lipid peroxidation in patients with AD; however, extensive studies on specific targets of lipid peroxidation‐induced damage are still missing. The present study represents a further step in understanding the relationship between oxidative modification of protein and neuronal death associated with AD. We used a proteomics approach to determine specific targets of lipid peroxidation in AD brain, both in hippocampus and inferior parietal lobule, by coupling immunochemical detection of 4‐hydroxynonenal‐bound proteins with 2‐D polyacrylamide gel electrophoresis and MS analysis. We identified 4‐hydroxynonenal‐bound proteins in the hippocampus and inferior parietal lobule brain regions of subjects with AD. The identified proteins play different biological functions including energy metabolism, antioxidant system, and structural proteins, thus impairing multiple molecular pathways. Our results provide further evidence for the role of lipid peroxidation in the pathogenesis of AD.
Keywords:4‐Hydroxynonenal  Alzheimer's disease  Lipid peroxidation  Protein oxidation  Redox proteomics
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