Cited by 311Redox biology and oxidative stressAntioxidant Activity and Oxidative StressAdvanced Glycation End Products research

Modification of glucose-6-phosphate dehydrogenase by 4-hydroxy-2-nonenal. Formation of cross-linked protein that inhibits the multicatalytic protease.

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Friguet, B., Stadtman, E.R., Szweda, L.I.·1994·Journal of Biological Chemistry

Abstract

Incubation of glucose-6-phosphate dehydrogenase (Glu-6-PDH) from Leuconostoc mesenteroides with the lipid peroxidation product 4-hydroxy-2-nonenal leads to the formation of cross-linked protein.This is accompanied by the appearance of protein-associated fluorescence with excitation and emission maxima of 340 and 415 nm, respectively, and with the disappearance of histidine and lysine residues.Cross-linked protein is less susceptible than native Glu-6-PDH to proteolysis by the multicatalytic protease, a multienzymic proteolytic complex involved in the intracellular degradation of damaged proteins.In addition, 4-hydroxy-2-nonenalmodified Glu-6-PDH inhibits the multicatalytic protease and can therefore prevent the efficient degradation of oxidized protein.These findings may have important implications for the accumulation of altered protein and fluorescent material in uiuo, processes that are believed to be involved in age-and disease-related impairment of cellular function.Reactive oxygen species readily interact with polyunsaturated fatty acids, often resulting in the formation of cytotoxic aldehydes such as 4-hydroxy-2-nonenal (HNE)l and malondialdehyde (for review see Ref. 1).Modification of various biomolecules by these lipid peroxidation products has been implicated in a number of degenerative diseases associated with aging (2-5) and is believed to result in the formation of fluorescent material that accumulates in a variety of postmitotic cells as they age (6-13).These results have led many to postulate a role for lipid peroxidation in the aging process.There is little direct evidence, however, primarily because the chemical nature of various modifications and the effects on cellular function are not well understood.Information on the mechanisms by which lipid peroxidation products react with biological materials is required for the development of reliable methods for detection of specific modifications in various tissue preparations.Identification of cellular targets and elucidation of the properties of modified biomolecules should provide insight into mechanisms by which these processes contribute to the pathophysiology of aging.HNE, a major product of lipid peroxidation, is significantly more reactive under physiological conditions than many other * The costs of publication of this article were defrayed in part by the payment of page charges.This article must therefore be hereby marked "aduertisement" in accordance with 18 U.S.C.Section 1734 solely to indicate this fact.

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  • The multiple higher mass electrophoretic components containing tissue metalloproteinase inhibitor 3 and vitronectin suggest the presence of covalent crosslinks.

    “The multiple, higher mass electrophoretic components containing these proteins suggest the presence of covalent crosslinks, protein modifications that can be caused by reactive lipid and carbohydrate oxidation products (22, 23).”

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References 38 · Cited by 311

Research works printed but not linked: 3

  1. Tappel, A. L. (1980) in Free Radicals in Biology (Pryor, W. A,, ed) vol. 4, pp.
  2. Esterbauer, H., Koller, E., Slee, R. G., and Koster, J. F. (1986) Biochem. J. 239, 9. Kikugawa, K, and Beppu, M. (1987) Chem. Phys. Lipids 44, 277-296 2-47, Academic Press, New York 405-409
  3. Carney, J. M., Starke-Reed, P. E., Oliver, C. N., Landum, R. W., Cheng, M. S., Wu, J. F., and Floyd, R. A. (1991) Proc. Natl. Acad. Sei. U. S. A. 88, 3633- 3636 3-15, Plenum Press, New York Commun. 69,896901 7,521-536

Authors
Friguet, B., Stadtman, E. R., & Szweda, L. I.
Affiliations
National Institutes of Health (US)
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1994-08
Volume
269
Issue
34
Pages
21639-21643
ISSN
0021-9258 (ISSN-L)
OpenAlex
W1522000230
Cited by
311
References
38
Citations by year
2026: 2 · 2025: 3 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 3 · 2020: 3 · 2019: 4 · 2018: 3 · 2017: 6 · 2016: 5 · 2015: 5 · 2014: 7 · 2013: 15 · 2012: 13
FWCI
2.53
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
  • Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
Keywords
glucose-6-phosphate dehydrogenase, 4-hydroxynonenal, lipid peroxidation, protein cross-linking, protease inhibition, protein fluorescence, protein degradation, aging, reactive oxygen species, Leuconostoc mesenteroides, malondialdehyde
MeSH terms
Aldehydes, Amino Acids, Animals, Cross-Linking Reagents, Cysteine Endopeptidases, Glucosephosphate Dehydrogenase, Leuconostoc, Liver, Models, Chemical, Multienzyme Complexes, Protease Inhibitors, Spectrometry, Fluorescence, Spectrophotometry, Proteasome Endopeptidase Complex, Rats

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