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      Protein lipoxidation: Detection strategies and challenges

      review-article
      a , b , c , b , a , d , d , d , *
      Redox Biology
      Elsevier
      Mass spectrometry, Reactive carbonyl species, Electrophilic lipids, Cyclopentenone prostaglandins, Target validation, Vimentin cysteine lipoxidation, ACR, acrolein, AGE, advanced glycation end product(s), ALE, advanced lipoxidation end product(s), CID, collisional induced dissociation, CHH, 7-(diethylamino)coumarin-3-carbohydrazide, cyPG, cyclopentenone prostaglandin(s), DNPH, 2,4-dinitrophenylhydrazine, ESI, electrospray ionization, GO, glyoxal, 4-HHE, 4-hydroxyhexanal, HNE, 4-hydroxynonenal, HEL, Nε-hexanoyl-lysine, MALDI, matrix assisted laser desorption/ionization, MDA, malondialdehyde, MS, mass spectrometry, NLS, neutral loss scans, ONE, 4-oxononenal, 15d-PGJ2, 15-deoxy-Δ12,14-prostaglandin J2, RCS, reactive carbonyl species.

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          Abstract

          Enzymatic and non-enzymatic lipid metabolism can give rise to reactive species that may covalently modify cellular or plasma proteins through a process known as lipoxidation. Under basal conditions, protein lipoxidation can contribute to normal cell homeostasis and participate in signaling or adaptive mechanisms, as exemplified by lipoxidation of Ras proteins or of the cytoskeletal protein vimentin, both of which behave as sensors of electrophilic species. Nevertheless, increased lipoxidation under pathological conditions may lead to deleterious effects on protein structure or aggregation. This can result in impaired degradation and accumulation of abnormally folded proteins contributing to pathophysiology, as may occur in neurodegenerative diseases. Identification of the protein targets of lipoxidation and its functional consequences under pathophysiological situations can unveil the modification patterns associated with the various outcomes, as well as preventive strategies or potential therapeutic targets. Given the wide structural variability of lipid moieties involved in lipoxidation, highly sensitive and specific methods for its detection are required. Derivatization of reactive carbonyl species is instrumental in the detection of adducts retaining carbonyl groups. In addition, use of tagged derivatives of electrophilic lipids enables enrichment of lipoxidized proteins or peptides. Ultimate confirmation of lipoxidation requires high resolution mass spectrometry approaches to unequivocally identify the adduct and the targeted residue. Moreover, rigorous validation of the targets identified and assessment of the functional consequences of these modifications are essential. Here we present an update on methods to approach the complex field of lipoxidation along with validation strategies and functional assays illustrated with well-studied lipoxidation targets.

          Graphical abstract

          Highlights

          • Protein lipoxidation may regulate protein activity in health and disease.

          • Lipoxidation by structurally diverse moieties may elicit specific functional outcomes.

          • The study of lipoxidation requires derivatization strategies and high resolution MS.

          • Lipoxidation functional assessment requires molecular and cellular biology approaches.

          • Importance of considering the potential interplay with other oxidative modifications.

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          Most cited references114

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          Lipid peroxidation: physiological levels and dual biological effects.

          Etsuo Niki (2009)
          Lipid peroxidation (LPO) has been shown to induce disturbance of membrane organization and functional loss and modification of proteins and DNA bases, and it has been implicated in the pathogenesis of various diseases. At the same time, LPO products have been shown to act as redox signaling mediators. Free and ester forms of both polyunsaturated fatty acids and cholesterol are important substrates for LPO in vivo and they are oxidized by both enzymatic and nonenzymatic mechanisms to give a variety of products. The results of numerous studies reported in the literatures show that the levels of LPO products in plasma of healthy human subjects are below 1 muM and that the molar ratios of LPO products to the respective parent lipids are below 1/1000, that is, below 0.1%. The levels of LPO products in human erythrocytes were found to be higher than those in plasma. Considerable levels of cholesterol oxidation products were observed. Although many LPO products exert cytotoxicity, sublethal concentrations of LPO products induce cellular adaptive responses and enhance tolerance against subsequent oxidative stress through upregulation of antioxidant compounds and enzymes. This adaptive response is observed not only for chemically reactive alpha,beta-unsaturated carbonyl compounds such as 4-hydroxy-2-nonenal and 15-deoxy-delta-12,14-prostaglandin J(2) but also for chemically stable compounds such as hydroxyoctadecadienoic acid, hydroxylcholesterol, and lysophosphatidylcholine. Such opposite dual functions of LPO products imply that LPO, and probably oxidative stress in general, may exert both deleterious and beneficial effects in vivo. LPO as well as reactive oxygen and nitrogen species has been shown to play an important role as a regulator of gene expression and cellular signaling messenger. In order to exert physiologically important functions as a regulator of gene expression and mediator of cellular signaling, the formation of LPO products must be strictly controlled and programmed. In contrast to LPO products by enzymatic oxidation, it appears difficult to regulate the formation of free radical-mediated LPO products. Even such unregulated LPO products may exert beneficial effects at low levels, but excessive unregulated LPO may lead to pathological disorders and diseases.
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            Protein carbonylation as a major hallmark of oxidative damage: update of analytical strategies.

            Protein carbonylation, one of the most harmful irreversible oxidative protein modifications, is considered as a major hallmark of oxidative stress-related disorders. Protein carbonyl measurements are often performed to assess the extent of oxidative stress in the context of cellular damage, aging and several age-related disorders. A wide variety of analytical techniques are available to detect and quantify protein-bound carbonyls generated by metal-catalyzed oxidation, lipid peroxidation or glycation/glycoxidation. Here we review current analytical approaches for protein carbonyl detection with a special focus on mass spectrometry-based techniques. The utility of several carbonyl-derivatization reagents, enrichment protocols and especially advanced mass spectrometry techniques are compared and discussed in detail. Furthermore, the mechanisms and biology of protein carbonylation are summarized based on recent high-throughput proteomics data. Copyright © 2013 Wiley Periodicals, Inc.
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              Chemistry of phospholipid oxidation.

              The oxidation of lipids has long been a topic of interest in biological and food sciences, and the fundamental principles of non-enzymatic free radical attack on phospholipids are well established, although questions about detail of the mechanisms remain. The number of end products that are formed following the initiation of phospholipid peroxidation is large, and is continually growing as new structures of oxidized phospholipids are elucidated. Common products are phospholipids with esterified isoprostane-like structures and chain-shortened products containing hydroxy, carbonyl or carboxylic acid groups; the carbonyl-containing compounds are reactive and readily form adducts with proteins and other biomolecules. Phospholipids can also be attacked by reactive nitrogen and chlorine species, further expanding the range of products to nitrated and chlorinated phospholipids. Key to understanding the mechanisms of oxidation is the development of advanced and sensitive technologies that enable structural elucidation. Tandem mass spectrometry has proved invaluable in this respect and is generally the method of choice for structural work. A number of studies have investigated whether individual oxidized phospholipid products occur in vivo, and mass spectrometry techniques have been instrumental in detecting a variety of oxidation products in biological samples such as atherosclerotic plaque material, brain tissue, intestinal tissue and plasma, although relatively few have achieved an absolute quantitative analysis. The levels of oxidized phospholipids in vivo is a critical question, as there is now substantial evidence that many of these compounds are bioactive and could contribute to pathology. The challenges for the future will be to adopt lipidomic approaches to map the profile of oxidized phospholipid formation in different biological conditions, and relate this to their effects in vivo. This article is part of a Special Issue entitled: Oxidized phospholipids-their properties and interactions with proteins. Copyright © 2012 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Redox Biol
                Redox Biol
                Redox Biology
                Elsevier
                2213-2317
                21 May 2015
                August 2015
                21 May 2015
                : 5
                : 253-266
                Affiliations
                [a ]Department of Pharmaceutical Sciences, Università degli Studi di Milano, Via Mangiagalli 25, 20133 Milan, Italy
                [b ]Mass Spectrometry Centre, QOPNA, Department of Chemistry, University of Aveiro, Aveiro 3810-193, Portugal
                [c ]School of Life and Health Sciences, Aston Triangle, Aston University, Birmingham B4 7ET, UK
                [d ]Department of Chemical and Physical Biology, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu, 9, Madrid 28040, Spain
                Author notes
                [* ]Corresponding author. dperezsala@ 123456cib.csic.es
                Article
                S2213-2317(15)00046-4
                10.1016/j.redox.2015.05.003
                4477048
                26072467
                40aeeab7-076f-4011-a4bc-5896464e111e
                © 2015 Published by Elsevier B.V.
                History
                : 13 April 2015
                : 14 May 2015
                : 19 May 2015
                Categories
                Review Article

                mass spectrometry,reactive carbonyl species,electrophilic lipids,cyclopentenone prostaglandins,target validation,vimentin cysteine lipoxidation,acr, acrolein,age, advanced glycation end product(s),ale, advanced lipoxidation end product(s),cid, collisional induced dissociation,chh, 7-(diethylamino)coumarin-3-carbohydrazide,cypg, cyclopentenone prostaglandin(s),dnph, 2,4-dinitrophenylhydrazine,esi, electrospray ionization,go, glyoxal,4-hhe, 4-hydroxyhexanal,hne, 4-hydroxynonenal,hel, nε-hexanoyl-lysine,maldi, matrix assisted laser desorption/ionization,mda, malondialdehyde,ms, mass spectrometry,nls, neutral loss scans,one, 4-oxononenal,15d-pgj2, 15-deoxy-δ12,14-prostaglandin j2,rcs, reactive carbonyl species.

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