Fundamentals on the biochemistry of peroxynitrite and protein tyrosine nitration.

In this review we provide an analysis of the biochemistry of peroxynitrite and tyrosine nitration. Peroxynitrite is the product of the diffusion-controlled reaction between superoxide (O2•-) and nitric oxide (•NO). This process is in competition with the enzymatic dismutation of O2•- and the diffusion of •NO across cells and tissues and its reaction with molecular targets (e.g. guanylate cyclase). Understanding the kinetics and compartmentalization of the O2•- / •NO interplay is critical to rationalize the shift of •NO from a physiological mediator to a cytotoxic intermediate. Once formed, peroxynitrite (ONOO- and ONOOH; pKa = 6,8) behaves as a strong one and two-electron oxidant towards a series of biomolecules including transition metal centers and thiols. In addition, peroxynitrite anion can secondarily evolve to secondary radicals either via its fast reaction with CO2 or through proton-catalyzed homolysis. Thus, peroxynitrite can participate in direct (bimolecular) and indirect (through secondary radical intermediates) oxidation reactions; through these processes peroxynitrite can participate as cytotoxic effector molecule against invading pathogens and/or as an endogenous pathogenic mediator. Peroxynitrite can cause protein tyrosine nitration in vitro and in vivo. Indeed, tyrosine nitration is a hallmark of the reactions of •NO-derived oxidants in cells and tissues and serves as a biomarker of oxidative damage. Protein tyrosine nitration can mediate changes in protein structure and function that affect cell homeostasis. Tyrosine nitration in biological systems is a free radical process that can be promoted either by peroxynitrite-derived radicals or by other related •NO-dependent oxidative processes. Recently, mechanisms responsible of tyrosine nitration in hydrophobic biostructures such as membranes and lipoproteins have been assessed and involve the parallel occurrence and connection with lipid peroxidation. Experimental strategies to reveal the proximal oxidizing mechanism during tyrosine nitration in given pathophysiologically-relevant conditions include mapping and identification of the tyrosine nitration sites in specific proteins.

Introduction

Oxidants and free radical species are physiologically and continuously formed in cells [1], [2], and can participate in redox signaling [3], [4]; however, under pathological conditions the formation of these species may significantly increase and mediate oxidative damage of different biomolecules such as lipids, sugars, DNA and proteins [5], [6], [7].

At a cellular level there are several sources of oxidants and free radical species, mainly based on the action of different enzymes present in plasma membrane (lipoxygenase, prostaglandin synthase, NADPH oxidase), mitochondrial electron transport chain (NADH dehydrogenase, ubiquinone), peroxisomes (oxidases and flavoproteins), endoplasmic reticulum and nuclear membrane (cytochrome P450 and cytochrome b5) and other enzymes such as oxidoreductases (xanthine oxidase, myeloperoxidase, P450 enzymes) or soluble heme-proteins (hemoglobin, myoglobin, cytochrome c). Lipid peroxidation in membranes is an important source of free radical species. Importantly, the family of nitric oxide synthases (NOS), generate the relatively stable and signal transducing free radical, nitric oxide (•NO), and NADPH oxidases family (NOX) among other enzymes produce superoxide radical anion (O2•-) [8], [9]. Finally, oxidants can be formed by the action of environmental factors such as, high energy irradiation, air pollutants, toxic chemicals and drug metabolism.

By the action of these enzymatic and non-enzymatic pathways several biologically-relevant oxidants can be formed including O2•-, hydrogen peroxide (H2O2) hypochlorite (HOCl) and hypobromide (HOBr), singlet oxygen (1O2), hydroxyl radical (•OH), peroxynitrite (ONOO-), nitrogen dioxide (•NO2) and carbonate radical (CO3•-) among others (Fig. 1). The production of these species can be enhanced in the presence of redox-active transition metal centers such as Fe3+, Cu2+, which in turn can potentiate the effect of oxidants (e.g. catalysis of nitration reactions) [1], [2].

Fig. 1

Main sources of oxidants and the O•- /•NO interplay. Free radicals can be formed by a variety of intra and extracellular sources. The simultaneous generation of nitric oxide and superoxide radicals yields peroxynitrite. Both, peroxynitrite and its secondary oxidants can mediate oxidative modifications in biomolecules. Antioxidant enzyme systems such as SOD, or peroxiredoxins (PRX) participate in controlling steady state levels of peroxynitrite. Other peroxidatic systems include catalase (CAT) and glutathione peroxidase (GPX).

In this chapter, we will focus on the interplay that exists between the •NO and O2•- routes for the generation of strongly oxidizing and nitrating species, which are connected through the formation of peroxynitrite (Fig. 1).

Several enzymatic antioxidant systems are present in cells to catabolize oxidants such as superoxide dismutase (SOD) [10], [11], which catalyzes superoxide dismutation to hydrogen peroxide, glutathione peroxidases (GPX), catalase (CAT) [12] and peroxiredoxins (PRX), which altogether remove hydrogen peroxide, peroxynitrite and lipid peroxides in various cellular compartments [13], [14], [15]. In the context of the O2•-/•NO interplay, SODs inhibit the formation of peroxynitrite and cytosolic and mitochondrial peroxiredoxins typically have an extraordinary catalytic ability to reduce it to nitrite (NO2-) [16].

Nitric oxide, superoxide and peroxynitrite

Nitric oxide (•NO), a relatively stable free radical formed in vivo, is a pleiotropic regulator and effector of the immune, cardiovascular and nervous system. In the early 80 s, the chemical nature of this molecule was still unknown, and its effects were ascribed to the endothelium-derived relaxing factor (EDRF) (for a review see [6]). At the end of that decade, EDRF identity was finally elucidated, and defined as •NO by Moncada et al. and Ignarro et al. [17], [18].

Nitric oxide can play regulatory functions by acting on vascular tone and plasticity [19], as a mediator at central nervous system and by inhibiting platelet aggregation [20]. It also can act as a protective agent by its antioxidant activity, mainly as a chain termination agent in lipid peroxidation reactions, inhibition of leukocyte adhesion and antimicrobial action [20]. In addition, •NO may play a deleterious role inhibiting enzyme function, promoting DNA damage or participating in pro-oxidant processes through the formation of •NO-derived oxidants. The action of •NO as a signaling molecule or cytotoxic agent largely depends its concentration and the redox environment present at the time. Most of •NO-derived toxicity in the context of oxidative stress conditions is due to the formation of •NO-derived oxidants, which are further more reactive than •NO itself [21].

Nitric oxide is synthetized by a family of enzymes called nitric oxide synthases (NOS) from l-arginine, NADPH, O2 and substrates FAD and FMN, using tetrahydrobiopterin (BH4) and calmodulin as cofactors [22], [23]. Three NOS isoforms have been isolated and characterized: neuronal NOS (nNOS), inducible NOS (iNOS) and endothelial NOS (eNOS) [22], [23], [24]. The presence of a mitochondrial NOS has been described, however, there is still no agreement in the presence of this isoform [25].

The chemistry of •NO dictates much of its biological activity [5], [6], [7], [20]. Nitric oxide may undergo autoxidation reactions in the presence of oxygen, leading to •NO2 formation, a strong oxidizing and nitrating agent (E°' •NO2/NO2- = 0.99 V). However, under normal conditions this is a rather slow termolecular process (k = 2.8 × 106 M−2 s−1) [26]. Nitrogen dioxide, may further react with •NO, forming dinitrogen trioxide (N2O3), an unstable species which mainly mediates nitrosation and deamination reactions [7]. In addition, •NO2 is present in pollution and cigarette smoke, playing an important role in environmental toxicity [27]. Autoxidation reactions are usually favored in hydrophobic environments such as lipoproteins and membranes, where •NO and O2 concentration may be higher than in aqueous solutions [28], [29].

Nitric oxide, is neither a strong oxidant (Eo' •NO/NO- = 0.39 V) nor a strong reductant (Eo' •NO/NO+ = 1.21 V) [30], [31] and therefore is not reactive with most of the biological molecules in spite of its radical nature. Nitric oxide does react fast with oxygen-, carbon-, sulfur- and nitrogen-centered radicals, such as O2•-, •OH, tyrosyl (Tyr•), thiyl (RS•), •NO2 and peroxyl (ROO•) radicals.

In the reaction with ROO•, nitrosated and nitrated lipids can be formed, in radical-radical termination reactions, accounting this way for some of its antioxidant properties [32].

Importantly, •NO has direct signaling effects by its reversible reaction with metal complexes of enzymes forming heme-nitrosyl complexes. This is the case of the reaction with guanylate cyclase (i.e. stimulates formation of cGMP) [33] or cytochrome aa3 (i.e. inhibits oxygen binding) [34]. An important •NO pathway in the vasculature, is its reaction with oxyhemoglobin (Hb2+-O2) and formation of methemoglobin (Hb3+) and NO3-. Due to the large amounts of Hb2+-O2 in red blood cells, this is an important intravascular reaction and sink for •NO produced in tissues [6].

Due to its hydrophobicity, small size and neutral condition, •NO has the ability of freely diffusing towards membranes, and it can react far away from its site of formation (100 µm – 1 mm) having quite long half life compared to other free radicals (1–10 s) [24].

Superoxide radical is a short-lived free radical, which may act either as an oxidant (E°’ O2•-/ H2O2 = 0.94 V) or reductant (Eo' O2/O2•- = 0.33 V). In cells, superoxide is formed by the action of several enzymes such as oxygenases, flavoproteins, xanthine oxidase, NADPH oxidases, uncoupled NOS and Complex I and III of the mitochondrial electron transport chain, among others [10], [11].

Under oxidative conditions, the interplay between the formation pathways of •NO and O2•- will play an important role in the mediation of cellular toxicity. In particular, the fast reaction of •NO with O2•- leading to the formation of peroxynitrite (ONOO-), which in turn will promote oxidation and nitration reactions affecting different biomolecules [7] (Fig. 2).

Fig. 2

Representative peroxynitrite-mediated oxidative modifications of biomolecules and its products. Modifications on proteins, lipids, sugars and DNA include those directly mediated by peroxynitrite or indirectly by peroxynitrite-derived radicals [7].

A central point to consider when invoking peroxynitrite as a mediator of oxidative effects of O2•- and •NO, relates to the kinetic competitiveness of the peroxynitrite formation reaction in biological systems. Indeed, once O2•- is formed, it may undergo the SOD-catalyzed dismutation reaction to H2O2 (kSOD = 2 × 109 M−1 s−1) [35], or react with •NO (kNO = 1 × 1010 M−1 s−1) [36] in a potentially faster reaction when •NO concentration increases. Therefore, in quantitative terms, the fate of O2•- radicals will mainly depend on the competition between two reactions: i) superoxide dismutation and ii) peroxynitrite formation; the ratio of this competition is relevant to determine the switch from signaling pathways of •NO to oxidative damage [37]. Still, it is important to consider that small amounts of O2•- will have secondary targets such as Fe-S centers present in proteins and enzymes (e.g. aconitase, producing cluster disruption) [38], free radicals (e.g. Tyr• leading to the formation of tyrosine hydroperoxide (Tyr-OOH) [39]), or transition metals present in low molecular weight complexes or proteins (e.g. O2•- favors iron release form ferritin) [40], which can disturb cell/tissue homeostasis due to the promotion of undesired transition metal mobilization and reactions (Fig. 3).

Fig. 3

Fates of superoxide in the presence of nitric oxide. Competition between O2•- dismutation and ONOO- formation is shown. Alternative reactions of O2•- are indicated with dashed arrows.

Peroxynitrite (ONOO-/ONOOH, pKa = 6.8) is a powerful and short-lived (half life ca. 10 ms) [41] oxidant formed in vivo, that can directly react with different biomolecules by one (i.e. reaction with transition metals) or two-electron (i.e. reaction with thiols) oxidations [42]. In addition, it can decompose by homolysis of peroxynitrous acid (ONOOH), to •NO2 and •OH radicals (in 30% yield), species that can further participate in nitration/oxidation reactions [41], [43], [44], a process that is relatively slow in biological systems [45]. One of the most important reactions of ONOO- in biological systems is its reaction with carbon dioxide (CO2), in equilibrium with bicarbonate (HCO3-) [46], and the concomitant formation of •NO2 and CO3•- radicals (in 35% yield), highly oxidant species that can in turn mediate oxidative damage to biomolecules [47]. An important aspect to take into account, is that peroxynitrite can mediate oxidations in aqueous phases (i.e. with, thiols, metalloproteins and CO2), or very importantly, freely diffuse through membranes (ONOOH), and react via its secondary radicals with lipids and proteins present in the hydrophobic milieu (Fig. 4) [48]. This may have particular relevance in lipid peroxidation reactions as will be discussed next.

Fig. 4

Fates of Peroxynitrite. Peroxynitrite can mediate direct or indirect reactions via its derived radicals, either in the aqueous phase or within membranes, promoting modifications in lipids and proteins.

Peroxynitrite-mediated reactions

Direct oxidation reactions

Thiols

One important peroxynitrite-mediated oxidation is its reaction with low molecular-weight or protein thiols, as described by Radi in 1991, who showed the reaction of peroxynitrite with free cysteine (k = 5900 M−1 s−1) [49], or the bovine serum albumim (BSA) thiol (Cys34) (k = 2800 M−1 s−1) at pH 7.4 and 37 °C. Later on, the reaction constant of peroxynitrite and human serum albumin (HSA) thiol was determined (k = 3800 M−1 s−1) at pH 7.4 and 37 °C [50].

Peroxynitrite reacts directly with thiols in a two-electron oxidation process involving a nucleophilic attack of the thiolate to the protonated form of peroxynitrite, ONOOH. The reaction yields nitrite and sulfenic acid (RSOH), which can in turn react with another thiol forming a disulfide (RSSR) [51] or become stabilized in special environments such as HSA [52]. In addition, peroxynitrite-derived radicals may react with thiols in one-electron oxidation reactions, yielding thiyl radicals (RS•), an oxidizing radical that can recombine with another RS• radical to form disulfides (RSSR), or initiate oxygen-dependent chain reactions that can produce thiyl-peroxyl radicals (RSOO•) and sulfinyl radicals (RSO•), among other products. It is important to consider that peroxynitrite chemistry leads to the formation of further oxidant species that can in turn mediate cellular damage.

In addition to cysteine, a few amino acids can be directly oxidized by peroxynitrite, namely methionine (k = 1.7–1.8 × 102 M−1 s−1) [53] and tryptophan (k = 37 M−1s−1) [54], [55].

Peroxynitrite does not directly react with tyrosine residues, however peroyxnitrite-derived radicals •OH, •NO2 and CO3•- play a critical role on tyrosine oxidation / nitration reactions, that will be described in the following section. Phenylalanine and histidine can also be modified by the action of peroxynitrite-derived radicals.

The oxidation of thiols and other amino acids by peroxynitrite may have an important impact on protein structure and function [41].

Metals

Peroxynitrite can react with transition metal centers such as iron, copper and manganese ions, forming part of proteins or low molecular weight complexes. The oxidation may take place through one-electron pathways yielding NO2- (e.g. heme proteins) or through two-electron reactions yielding •NO2 and the oxidized metal [37]. Some metal complexes can promote the isomerization of ONOO- to nitrate (NO3-). In enzymes such as myeloperoxidase (MPO), peroxynitrite reacts through a one-electron process with the iron, yielding •NO2 and an oxo-ferryl compound, also a powerful oxidant. In the presence of reductants such as glutathione or ascorbic acid, these oxidizing intermediates may be reduced to NO2- and the initial oxidation state of the metal center [41], [45].

Indirect oxidation reactions

Other biomolecules

Peroxynitrite-derived radicals, •OH, •NO2 can react in addition to amino acids, with lipids, sugars and nitrogen bases [7].

After ONOOH homolysis, •NO2 and •OH radical can readily initiate lipid peroxidation by one-electron abstraction on allylic hydrogen atoms in double bonds of unsaturated fatty acids [56]. The reaction of •NO and •NO2 with lipids, may lead to the formation of a variety of modified oxidized and nitrated fatty acids [57].

Peroxynitrite-derived radicals can also react with sugars present in monosaccharides (e.g. glucose) or polysaccharides (e.g. glycosaminoglycanes) [58]. The reaction of peroxynitrite with glycosaminoglycanes (GAGs) will result in extense polymer and fragmentation (hyaluronan, chondroitin and heparin, dermatan and heparan sulfates) [59]. DNA bases can also be affected by peroxynitrite-derived radicals in nitration and oxidation reactions. Peroxynitrite can promote guanine oxidation and nitration, being 8-oxo-guanine and 8-nitro-guanine main products of these reactions. Hydroxyl radical leads to DNA strands breaks. In addition, other reactive nitrogen species such as trioxide nitrogen may promote DNA deamination reactions [60], [61] (Fig. 2).

Carbon dioxide

The reaction of peroxynitrite and carbon dioxide, present at high concentrations (1.3 mM, in equilibrium with 25 mM bicarbonate anion) is one of the most important in biological systems. This reaction occurs through a nucleophilic addition of ONOO- to CO2 (k = 4.6 × 104 M−1 s−1) [62], [63], [64], [65] yielding a transient species, nitroso-peroxocarbonate (ONOOCO2-), which will decompose homolytically yielding •NO2 and CO3•- radicals. These radicals are short-lived one-electron oxidants that can promote themselves nitro-oxidative damage [45].

The case of protein tyrosine nitration

As mentioned above, peroxynitrite can mediate oxidative modifications in a variety of biomolecules. An important aspect of peroxy-nitrite-mediated toxicity is its capability of promoting protein tyrosine nitration, a covalent oxidative posttranslational modification mediated by nitric oxide-derived oxidants such as •NO2 and ONOO-.

Protein tyrosine nitration could result in dramatic changes in protein structure and can affect protein function either by a loss-(e.g. MnSOD, actin, prostacyclin synthase and tyrosine hydroxylase), or by a gain-of-a previously inexistent function (e.g. cytochrome c, fibrinogen, protein kinase, glutathione S-transferase and apoA1) [66]. It may alter phosphorylation cascades, or induce immunological responses by the generation of antibodies against nitrated proteins [66], [67], [68], [69].

Nitration as a free radical process

The nitration of protein tyrosine residues constitutes the substitution of a hydrogen by a nitro group (-NO2) in the position 3 of the phenolic ring, being 3-nitrotyrosine (3-NT) the product of this reaction.

Protein tyrosine nitration is a free radical-mediated pathway, which involves the intermediate formation of Tyr• radical from tyrosine [21], [69]. There are several oxidants that can perform the one-electron oxidation of tyrosine in biological systems, •OH, •NO2, CO3•- radicals, oxo-metal compounds (O=MnIV) and compounds I and II of hemoperoxidases, such as MPO. Moreover, we have recently demonstrated a “connection reaction” in membranes between lipid peroxidation and tyrosine oxidation, by which lipid-derived radicals, peroxyl (LOO•) [70] and alkoxyl (LO•) [71] can oxidize tyrosine to Tyr• in membranes, therefore promoting nitration reactions [67], [70], [72], [73].

Once Tyr• radical is formed it can have different fates, one of which in the context of peroxynitrite-dependent reaction is the diffusion-controlled reaction with •NO2 to yield 3-NT (Fig. 5). In addition to this product, other oxidation products can be formed. The combination of two Tyr• will lead to the formation of the dimerized form, 3,3′-dityrosine, the addition of •OH will yield 3,4-dihydroxyphenylalanine (DOPA) (also known as 3-hydroxytyrosine), and the reaction with O2•- radical produces tyrosine hydroperoxide. In addition, Tyr• can react with •NO, forming 3-nitrosotyrosine, which will further evolve to 3-NT formation [21], [69] (Fig. 5).

Fig. 5

Tyrosine oxidation pathways. Tyrosine can be oxidized by several oxidants to yield Tyr• (1), leading to 3-nitrotyrosine formation in the presence of •NO2 (2); nitrosotyrosine in reaction with •NO; 3,3′-dityrosine by combination with another Tyr• radical (5) or 3,4′-dihydroxyphenylalanine (DOPA) by a hydroxylation reaction, (X = OH), or 3-hydroperoxytyrosine by its reaction with O2• (X = OOH) (6).

It is important to consider that tyrosine oxidation reactions can be reversed by the repair of Tyr• radical (i.e. reducing it back to tyrosine), by the action of reductants such as glutathione or ascorbate, or through intramolecular electron transfer reactions with other amino acids, such as cysteine [74], [75].

Peroxynitrite-dependent and independent tyrosine nitration mechanisms

Protein tyrosine nitration is consistently observed in several pathologies such as cardiovascular disease [76], neurodegeneration [77], [78], [79], inflammation and cancer [80]. Indeed, protein 3-NT is established as a biomarker of oxidative stress in vivo, being revealed as a strong biomarker and predictor of disease onset and progression.

In addition to peroxynitrite, protein tyrosine nitration can occur by the action of enzymes such as MPO in the presence of NO2- and H2O2, a process that plays an important role during neutrophil degranulation in inflammation sites. In this tyrosine nitration mechanism, the MPO reaction with H2O2 yields compound I, a high oxidation state oxo-heme complex that oxidizes tyrosine to Tyr• radical and NO2- to •NO2, generating the proper combination of reagents to yield 3-NT [81]. Additional biological mechanisms of tyrosine nitration involve the action of NO2- under acidic conditions as observed in the gastric lumen [82], [83].

Nitration selectivity

Protein tyrosine nitration is a low yield process and is highly selective, since neither all proteins can become nitrated nor all tyrosine-residues within a particular protein can undergo nitration. Usually, in whole tissue/cell only 1–5 over 10,000 tyrosine residues become nitrated [21]. However, in some specific proteins, tyrosine nitration yields are large and responsible of structural and functional changes [21], [68], [69].

Several physicochemical factors control tyrosine nitration either in aqueous or hydrophobic environments, however, there is not a general rule to anticipate tyrosine nitration selectivity and each protein has to be specifically-analyzed.

The nitration of a particular tyrosine residue will depend on several factors including, protein structure, nitration mechanism, and the environment were the tyrosine residue is located [66], [67], [68], [84], [85].

Protein structure

Usually in aqueous solution and solvent-exposed tyrosine residues, nitration is enhanced in the presence of CO2, transition metal centers and the proximity of charged amino acids (through hydrogen-bonding) or binding sites for hemeperoxidases [68]. The presence of nearby turn-inducing amino acids such as proline and glycine usually favors nitration of nearby tyrosine residues as observed in RNAase A and lysozyme [84], [85].

The existence of a consensus sequence for tyrosine nitration has been proposed by some authors [84], however it has not been really demonstrated, and the secondary and tertiary structures and solvent accessibility appear to be the most important factors affecting tyrosine nitration selectivity.

However, the presence of some amino acids in the close proximity of tyrosine residues do affect nitration. This is the case of cysteine which can inhibit nitration due to intramolecular-electron transfer reactions between Tyr and Cys residues, as shown by studies in model peptides and proteins such as Fe-SOD present in T. cruzi [75], [86]. Nearby methionine residues could in turn, promote nitration also by intramolecular electron transfer reactions between Tyr and Met residues [87]. In addition, the presence of charged amino acids usually favor nitration reactions due the formation of hydrogen bonds. On the other hand, the presence of nearby positively-charged amino acids such as arginine, may inhibit tyrosine nitration due to electrostatic forces (e.g. Y20 and R21 in lysozyme) [85].

The location of the tyrosine residue within the protein turns to be critical in the possibility of a tyrosine residue in being nitrated. Buried tyrosine residues usually cannot accommodate the voluminous nitro group (-NO2) by a steric effect, while exposure of the aromatic ring of the tyrosine to the protein surface should facilitate the reaction. Solvent-exposed tyrosine residues are particularly sensitive in the presence of CO2 as observed for Y48, Y74 and Y97 of cytochrome c [88].

The redox environment of the particular tyrosine residue will determine as well the possibilities of nitration. The presence of endogenous antioxidants such as glutathione [45], [74], ascorbate [89], [90] and uric acid [45], [91] will inhibit nitration reactions by the consumption of oxidizing and nitrating species such as •NO2.

Nitration mechanism

In some cases, proximity of transition metals centers to tyrosine become the key selectivity element. The presence of a transition metal center may site-specifically direct nitration, as observed in Mn-SOD which is nitrated by peroxynitrite specifically on Y34 in active site, located 5 Å away for manganese atom [92], [93], [94] and Y192 in apoA1 located in the MPO-binding site region [95].

Nitration of Mn-SOD in Y34 present in the access channel for superoxide, will block the entrance of the channel and generates an electrostatic repulsion effect (as the pKa of the –OH group of tyrosine drops from pH 10.5 to 7–7.5 upon nitration) promoting the inactivation of the enzyme [68], [69].

In addition, tyrosine nitration may promote a gain of function, such is the case of the cytocrome c which after nitration displays a peroxidatic activity. Indeed, the nitration of solvent-exposed (Y74), triggers a conformational change on cytocrome c, resulting in an alternative conformation, which affects its normal electron transport function, and enhances a peroxidatic activity [69], [96].

In general, •NO2 tends to modify solvent-exposed tyrosines while transition metals can provide regio-selectivity for the nitration of internal or buried tyrosine residues.

Cellular and redox environments

In hydrophobic environments (i.e. membranes and lipoproteins), the physicochemical factors controlling nitration reactions may differ from those observed in aqueous solution, mainly due to the high concentration of unsaturated fatty acids, which may outcompete for the free radical species, the exclusion of antioxidants usually present in polar environments, such as glutathione (GSH), which usually acts inhibiting nitration due to its fast reaction with •NO2 (k = 5.3 × 106 M−1 s−1) [97], and the diffusion of •NO and •NO2, that easily diffuse towards lipid milieu, and partition in a favored manner compared to aqueous phases [28], [29]. In membranes, factors as interaction with water molecules, oxygen concentration and lipid-soluble antioxidants, in addition to phospholipid composition, should also be taken into account [68]. In these compartments, lipid peroxidation reactions may fuel nitration/oxidation pathways, since there is a contribution of lipid-derived radicals (i.e. LOO• and LO•) in the generation of Tyr•, due to the one-electron oxidation of tyrosine (Eq. (1)) [67], [70], [72].

While oxygen does not react with tyrosine or tyrosyl radicals, it becomes a critical factor in the modulation of tyrosine nitration in membranes [70], [72], via its participation in the propagation phase of lipid peroxidation, so the physicochemical properties of the milieu will also directly impact on tyrosine nitration [67]. Hydrophobic environments such as membranes or lipoproteins will limit the diffusion of charged reactive species (i.e. CO3•-) which are potent oxidants in the aqueous phase [98]. In addition there is an exclusion of hydrophilic anti-nitrating agents, such as glutathione, which reacts fast with •NO2. On the other hand, nitrating species such as •NO and •NO2, will easily diffuse and concentrate in hydrophobic media, favoring nitration pathways [99].

Changes in pH will influence peroxynitrite-dependent nitration yields [73] and acidic conditions favor nitrite-dependent nitration pathways as observed in pepsin [82].

Conclusions

Understanding the conditions that facilitate the biological formation of peroxynitrite, its preferential reactions with biomolecules and the main oxidation products generated require comprehension of kinetic, mechanistic and physico-chemical elements. Moreover, the redox processes that lead to protein tyrosine nitration are intimately associated with decay pathways of peroxynitrite, including the notable reaction with CO2, that simultaneously generate oxidizing and nitrating species. Peroxynitrite can be considered an unusual peroxide due to its intrinsic instability in biological systems, the coexistence of the anionic and protonated forms at physiological pH with distinctive reactivities and its capacity to readily trigger free radical processes. Among the latter, protein tyrosine nitration constitutes a hallmark of the actions of peroxynitrite and related •NO-derived oxidants in cells and tissues. While the biochemical routes leading to the formation of 3-NT in various cellular and extracellular compartments have been mostly settled, its impact in protein structure and function in vivo still requires substantially more research. The well-established association of protein tyrosine nitration to several pathologies, and even with the aging process, opens opportunities to unravel whether this oxidative posttranslational modification in specific proteins (and residues) can disrupt cell homeostasis. The fundamentals provided in this review may assist for stimulating further experimental designs, sample analysis and therapeutic developments directed to assess the role of peroxynitrite and protein tyrosine nitration in human disease and aging.