Cited by 270Alzheimer's disease research and treatmentsLipid Membrane Structure and BehaviorAntioxidant Activity and Oxidative Stress

The Lipid Peroxidation Product, 4‐Hydroxy‐2‐trans‐Nonenal, Alters the Conformation of Cortical Synaptosomal Membrane Proteins

Subramaniam, Ram, Roediger, Fred, Jordan, Brad, Mattson, Mark P., Keller, Jeffrey N., Waeg, Georg, Butterfield, D. Allan·1997·Journal of Neurochemistry

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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Crossref · 10.1046/j.1471-4159.1997.69031161.x

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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].”

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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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