The Lipid Peroxidation Product, 4‐Hydroxy‐2‐trans‐Nonenal, Alters the Conformation of Cortical Synaptosomal Membrane Proteins
Abstract
Alzheimer's disease (AD) is widely held to be a disorder associated with oxidative stress due, in part, to the membrane action of amyloid beta-peptide (A beta). A beta-associated free radicals cause lipid peroxidation, a major product of which is 4-hydroxy-2-trans-nonenal (HNE). We determined whether HNE would alter the conformation of synaptosomal membrane proteins, which might be related to the known neurotoxicity of A beta and HNE. Electron paramagnetic resonance spectroscopy, using a protein-specific spin label, MAL-6 (2,2,6,6-tetramethyl-4-maleimidopiperidin-1-oxyl), was used to probe conformational changes in gerbil cortical synaptosomal membrane proteins, and a lipid-specific stearic acid label, 5-nitroxide stearate, was used to probe for HNE-induced alterations in the fluidity of the bilayer domain of these membranes. Synaptosomal membranes, incubated with low concentrations of HNE, exhibited changes in protein conformation and bilayer order and motion (fluidity). The changes in protein conformation were found to be concentration- and time-dependent. Significant protein conformational changes were observed at physiologically relevant concentrations of 1-10 microM HNE, reminiscent of similar changes in synaptosomal membrane proteins from senile plaque- and A beta-rich AD hippocampal and inferior parietal brain regions. HNE-induced modifications in the physical state of gerbil synaptosomal membrane proteins were prevented completely by using excess glutathione ethyl ester, known to protect neurons from HNE-caused neurotoxicity. Membrane fluidity was found to increase at higher concentrations of HNE (50 microM). The results obtained are discussed with relevance to the hypothesis of A beta-induced free radical-mediated lipid peroxidation, leading to subsequent HNE-induced alterations in the structure and function of key membrane proteins with consequent neurotoxicity in AD brain.
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HNE binds to and changes the structure of proteins, altering protein conformation and causing loss of function.
“Protein conformation is also altered with loss of function by HNE that binds to and changes the structure of proteins [28].”
From Mitochondrial Oxidative and Nitrosative Stress and Alzheimer Disease (2020) · cites this paper as [28]
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References 39 · Cited by 270
- Authors
- Subramaniam, R., Roediger, F., Jordan, B., Mattson, M. P., Keller, J. N., Waeg, G., & Butterfield, D. A.
- Affiliations
- University of Kentucky (US)
- University of Graz (AT)
- Corresponding author
- Butterfield, D. Allan
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 1997-09
- Volume
- 69
- Issue
- 3
- Pages
- 1161-1169
- ISSN
- 0022-3042 (ISSN-L)
- 1471-4159
- OpenAlex
- W2022887646
- Cited by
- 270
- References
- 39
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 10 · 2022: 2 · 2021: 6 · 2020: 11 · 2019: 7 · 2018: 5 · 2017: 2 · 2016: 5 · 2015: 13 · 2014: 7 · 2013: 10 · 2012: 11
- FWCI
- 5.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (P01AG010836, P01AG005119, AG 10836, AG0 5119)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Keywords
- lipid peroxidation, Alzheimer's disease, amyloid-beta, protein conformation, membrane fluidity, oxidative stress, glutathione ethyl ester, neurotoxicity, free radicals
- MeSH terms
- Aldehydes, Animals, Cerebral Cortex, Cross-Linking Reagents, Cyclic N-Oxides, Dose-Response Relationship, Drug, Electron Spin Resonance Spectroscopy, Free Radicals, Gerbillinae, Intracellular Membranes, Kinetics, Male, Membrane Lipids, Membrane Proteins, Models, Chemical, Phospholipids, Protein Conformation, Spin Labels, Synaptosomes, Lipid Peroxidation
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