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Oxidation of low-density lipoprotein by hypochlorite causes aggregation that is mediated by modification of lysine residues rather than lipid oxidation
Open accessAbstract
Peroxidation of low-density lipoprotein (LDL) lipid is generally thought to represent the initial step in a series of modification reactions that ultimately transform the protein moiety of the lipoprotein into a form recognized by receptors different from those that bind native LDL. Uptake of LDL via these alternative receptors can lead to the formation of lipid-laden cells, which are typical for the early stages of atherogenesis. We have studied the oxidative modification of LDL by hypochlorite (-OCl), a powerful oxidant produced from H2O2 and chloride via the action of myeloperoxidase which is released from activated neutrophils and monocytes. Exposure of LDL to reagent or enzymically generated -OCl at 4 or 37 degrees C resulted in immediate and preferential oxidation of amino acid residues of apolipoprotein B-100, the single protein associated with LDL. Lysine residues quantitatively represented the major target and, like tryptophan, were oxidized to approximately the same extent with reagent or enzymically generated -OCl. In contrast, LDL lipid oxidation was less favoured than protein oxidation, as judged by the amounts of lipid hydroperoxides, chlorohydrins, cholesterol or fatty acid oxidation products formed. Treatment with -OCl caused aggregation of LDL, as shown by an increased turbidity of the oxidized LDL solution and elution from a size-exclusion h.p.l.c. column of high-molecular-mass LDL complexes. Chemical modification of lysine residues before oxidation with -OCl prevented aggregation, while it enhanced the extent of lipid peroxidation. Treatment of LDL with -OCl also caused the formation of carbonyl groups and release of ammonia; both these modifications were inhibited by lysine-residue modification before oxidation. These results demonstrate that aggregation reactions are dependent on initial lysine oxidation by -OCl, followed by deamination and carbonyl formation, but do not involve lipid (per)oxidation. We propose that the observed -OCl-mediated aggregation of LDL is caused, at least in part, by cross-linking of apoproteins by Schiff-base formation independently of lipid peroxidation.
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“Protein chlorination has been associated with structural changes of target proteins including fragmentation, crosslinking, aggregation, unfolding, and modulation of specific functions such as immunogenicity, enzymatic activity and ligand-receptor interaction (48, 79).”
From Hypochlorous Acid: From Innate Immune Factor and Environmental Toxicant to Chemopreventive Agent Targeting Solar UV-Induced Skin Cancer (2022) · cites this paper as [79]
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Cites
A SPECTROPHOTOMETRIC METHOD FOR MEASURING THE BREAKDOWN OF HYDROGEN PEROXIDE BY CATALASE
Beers, R. F., & Sizer, I. W. (1952) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50881-x · Cited by 6,781
Epstein, F. H., Steinberg, D. I., Parthasarathy, S., Carew, T. E., Khoo, J. C., & Witztum, J. L. (1989) · New England Journal of Medicine · doi:10.1056/nejm198904063201407 · Cited by 6,425
[49] Determination of carbonyl content in oxidatively modified proteins
Levine, R. L., Garland, D. L., Oliver, C. N., Amici, A., Climent, I., Lenz, A.-G., Ahn, B. W., Shaltiel, S., & Stadtman, E. R. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86141-h · Cited by 5,895
A Receptor-Mediated Pathway for Cholesterol Homeostasis
Brown, M. S., & Goldstein, J. L. (1986) · Science · doi:10.1126/science.3513311 · Cited by 5,703
Janero, D. R. (1990) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(90)90131-2 · Cited by 2,735
Goldstein, J. L., Ho, Y. K., Basu, S. K., & Brown, M. S. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.333 · Cited by 2,447
Ylä‐Herttuala, S., Palinski, W., Rosenfeld, M. E., Parthasarathy, S., Carew, T. E., Butler, S. S., Witztum, J. L., & Steinberg, D. H. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114271 · Cited by 1,877
Autoantibody against oxidised LDL and progression of carotid atherosclerosis
Salonen, J. T., Korpela, H., Salonen, R., Nyyssönen, K., Ylä‐Herttuala, S., Yamamoto, R., Butler, S., Palinski, W., & Witztum, J. L. (1992) · The Lancet · doi:10.1016/0140-6736(92)90926-t · Cited by 1,311
Antioxidant defenses and lipid peroxidation in human blood plasma.
Frei, B. B., Stocker, R., & Ames, B. N. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.24.9748 · Cited by 1,254
Studies on the chlorinating activity of myeloperoxidase.
Harrison, J., & Schultz, J. (1976) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)33749-3 · Cited by 925
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Szuchman-Sapir, A. J., Pattison, D. I., Davies, M. J., & Witting, P. K. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.09.023 · Cited by 12
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Shi, J. L., & Mitch, W. A. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.2c09556 · Cited by 12
Exner, M., Alt, E., Hermann, M., Hofbauer, R., Kapiotis, S., Quehenberger, P., Speiser, W., Minar, E., & Gmeiner, B. M. K. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)02131-7 · Cited by 11
In Vitro Cellular Assays for Oxidative Stress and Biomaterial Response
Mitov, M. I., Patil, V. S., Alstott, M. C., Dziubla, T. D., & Butterfield, D. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803269-5.00006-1 · Cited by 10
Reactive Oxygen and Nitrogen Species and Liver Ischemia-Reperfusion Injury: An Overview
Alban, F. T. E., Gyamfi, D., van Golen, R. F., & Heger, M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-803951-9.00008-2 · Cited by 11
New insights into the effects of the protein moiety of oxidized LDL (oxLDL)
Vicca, S., Massy, Z. A., Hennequin, C., Rihane, D., Nguyen‐Khoa, T., Drüeke, T. B., & Lacour, B. (2003) · Kidney International · doi:10.1046/j.1523-1755.63.s84.44.x · Cited by 10
The Human Eosinophil Proteome. Changes Induced by Birch Pollen Allergy
Woschnagg, C., Forsberg, J., Engström, Å., Odreman, F., Venge, P., & Garcia, R. C. (2009) · Journal of Proteome Research · doi:10.1021/pr800984e · Cited by 10
Modified Low-Density Lipoproteins and High-Density Lipoproteins
Koller, E., Volf, I., Gurvitz, A., & Koller, F. (2006) · Pathophysiology of Haemostasis and Thrombosis · doi:10.1159/000093225 · Cited by 10
Pentikäinen, M. O., Öörni, K., & Kovanen, P. T. (2001) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/hq1201.099423 · Cited by 10
Tertov, V. V., Kaplun, V. V., & Orekhov, A. N. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006811720282 · Cited by 10
Shimamura, Y., Oura, Y., Tsuchiya, M., Yamanashi, Y., Ogasawara, A., Oishi, M., Komuro, M., Sasaki, K., & Masuda, S. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1328055 · Cited by 9
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Amin, F., & Bano, B. (2018) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2018.1500946 · Cited by 9
Beta-blockers inhibit the modification of low-density lipoproteins by sodium hypochlorite in vitro
Seifert‐Held, T., Zschörnig, O., Arnhold, J., & Arnold, K. (1997) · Chemistry and Physics of Lipids · doi:10.1016/s0009-3084(96)02637-0 · Cited by 9
Effect of fluid mechanical stresses and plasma constituents on aggregation of LDL
Rm, T., del Rio, J. D., & Weinberg, P. D. (2003) · Journal of Lipid Research · doi:10.1194/jlr.m200477-jlr200 · Cited by 9
Visible light powered self-disinfecting coatings for influenza viruses
Weng, D., Qi, H., Wu, T.-T., Yan, M., Sun, R., & Lu, Y. (2012) · Nanoscale · doi:10.1039/c2nr30388d · Cited by 8
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Llorente‐Cortés, V., & Badimón, L. (1998) · Revista Española de Cardiología · doi:10.1016/s0300-8932(98)74802-x · Cited by 8
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Wang, H., Martin, M. W., & Yin, S.-A. (2010) · Czech Journal of Food Sciences · doi:10.17221/104/2009-cjfs · Cited by 7
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Grune, T., Catalgol, B., & Jung, T. (2012) · Wiley eBooks · doi:10.1002/9781118493038.ch1 · Cited by 7
Magon, N. J., Turner, R., Kettle, A. J., & Winterbourn, C. C. (2023) · Redox Biochemistry and Chemistry · doi:10.1016/j.rbc.2023.100002 · Cited by 6
Ahmad, P., Tantry, I. Q., Ali, A., Siddiqui, S. A., Rehman, S. U., Waris, S., & Jairajpuri, M. A. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108332 · Cited by 6
Wang, Y., Hammer, A., Höefler, G., Malle, E., Hawkins, C. L., Chuang, C. Y., & Davies, M. J. (2023) · Antioxidants · doi:10.3390/antiox12020420 · Cited by 5
Wang, H., Zhang, X., Li, P., Huang, F., Xiu, T., Wang, H., Zhang, W., Zhang, W., & Tang, B. (2023) · Angewandte Chemie · doi:10.1002/ange.202315861 · Cited by 5
Hartsema, E. A., Hemmling, H., & Hawkins, C. L. (2025) · Advances in Redox Research · doi:10.1016/j.arres.2025.100119 · Cited by 4
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Vellosa, J. C. R., Barbosa, F. D. D., de, O. M. M., & Oliveira, F. (2007) · Cited by 3
Belik, I. V., Ivantsova, A. A., Mamedova, Z. E., & Denisenko, A. D. (2016) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20166204471 · Cited by 3
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Rao, V. A. (2015) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-1-4939-2543-8_11 · Cited by 2
Jerlich, A., Hammel, M., Horáková, Ľ., & Schaur, R. J. (2001) · Redox Report · doi:10.1179/135100001101536319 · Cited by 2
McCall, M. R., & Frei, B. B. (2000) · Developments in cardiovascular medicine · doi:10.1007/978-1-4615-4649-8_5 · Cited by 2
Vellosa, J. C. R. (2008) · Americanae (AECID Library) · Cited by 2
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Antwerpen, P. V., Boudjeltia, K. Z., Vaes, M., Babar, S., Madhoun, P., Moguilevsky, N., Vanhaeverbeek, M., Nève, J., & Ducobu, J. (2006) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfl143 · Cited by 1
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(2005) · CRC Press eBooks · doi:10.1201/9781420030853.pt3 · Cited by 1
Belik, I. V., Ivantsova, A. A., Mamedova, Z. E., & Denisenko, A. D. (2016) · Biochemistry (Moscow) Supplement Series B Biomedical Chemistry · doi:10.1134/s1990750816040028 · Cited by 1
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Liu, G., Wu, H., Chai, X., Shao, Y., Hu, L., Liu, B., & Fang, J. (2011) · International Conference on Bioinformatics and Biomedical Engineering · doi:10.1109/icbbe.2011.5780161
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Af, R. (2022) · UNSWorks (UNSW Sydney) · doi:10.26190/unsworks/21514
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Constantinescu, P. (2015) · Research Online (University of Wollongong)
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Frei, B. B. (1998) · Springer eBooks · doi:10.1007/978-88-470-2244-7_7
Coremans, C., Boudjeltia, K. Z., Antwerpen, P. V., & Delporte, C. (2021) · CRC Press eBooks · doi:10.1201/9781003212287-9
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Kubala, L., & Lojek, A. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8399-0_5
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Gutierrez, B. (2021) · Scholarworks (University of Massachusetts Amherst) · doi:10.7275/6325158.0
Sharma, V. K. (2012) · Wiley eBooks · doi:10.1002/9781118482469.ch3
Resistance of native and circulating modified low-density lipoproteins in human blood to association
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Resistance of native and circulating modified low-density lipoproteins in human blood to association
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Brown, B. E. (2004) · The Sydney eScholarship Repository (The University of Sydney)
Heinecke, J. W. (1997) · Springer eBooks · doi:10.1007/978-94-017-1607-9_19
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Coker, M. S. A. (2011) · Otago University Research Archive (University of Otago)
Metadata
- Authors
- Hazell, L. J., van den Berg, J. J. M., & Stocker, R.
- Affiliations
- The Heart Research Institute (AU)
- Children's Hospital Oakland Research Institute, Oakland, CA 94609, U.S.
- Corresponding author
- Stocker, R
- ORCID
- Stocker, R
- Venue
- Biochemical Journal
- Publisher
- Portland Press Ltd.
- Published
- 1994-08-15
- Volume
- 302
- Issue
- 1
- Pages
- 297-304
- ISSN
- 0264-6021 (ISSN-L)
- 1470-8728
- PMC
- PMC1137223
- OpenAlex
- W2142527036
- Cited by
- 267
- References
- 44
- Citations by year
- 2025: 2 · 2024: 4 · 2023: 5 · 2022: 3 · 2021: 6 · 2020: 7 · 2019: 4 · 2018: 6 · 2017: 5 · 2016: 11 · 2015: 5 · 2014: 6 · 2013: 7 · 2012: 9
- FWCI
- 5.61
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Biochemical Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Health and Human Services
- Tobacco-Related Disease Research Program
- National Institutes of Health (5r01dk034400-10)
- Medical Research Council
- National Health and Medical Research Council
- National Institute of Diabetes and Digestive and Kidney Diseases (P01DK032094, DK-34400, DK32094)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- LDL oxidation, hypochlorite, lysine oxidation, LDL aggregation, apolipoprotein B-100, lipid peroxidation, myeloperoxidase, atherogenesis, Schiff base formation, protein cross-linking, carbonyl formation, tryptophan oxidation, lipid hydroperoxides, neutrophils, monocytes
- MeSH terms
- Adult, Female, Humans, Hypochlorous Acid, Lipoproteins, LDL, Lysine, Male, Oxidation-Reduction
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