Kinetics of the co-operative reaction of Helix pomatia hemocyanin with oxygen. Oxygen binding at low and intermediate oxygen saturations

The kinetics of oxygen binding of Helix pomatia α-hemocyanin has been studied at low and intermediate levels of ligand saturation, under conditions in which oxygen binding is highly co-operative. Temperature-jump relaxation spectra are heterogeneous and can be resolved into a slow and a fast phase. The latter is related to a bimolecular reaction, i.e. the binding of oxygen. At very low degrees of fractional saturation (<0.15) the reactant concentration-dependence of the faster relaxation rate allows the combination and dissociation rate constants of the low affinity or T-state to be estimated as 1.3 × 10⁶m^?1 s^?1 and 300 s^?1, respectively. A possible interpretation of the slow component in the relaxation spectrum is discussed.In stopped-flow experiments, after mixing deoxyhemocyanin with oxygen-containing buffer, most of the binding process to the T-state is lost in the dead time. The observed initial rates of oxygen binding are between 15 and 120 s^?1. depending on the oxygen concentration, and may reflect the rate of the allosteric change from a low to a high affinity state (T→R transition), which is slower than oxygen binding.Similarities and differences in the overall kinetic properties of small and giant respiratory proteins, i.e. hemoglobin and hemocyanin, are discussed.     

Nitric oxide from nitrite reduction by hemoglobin in the plasma and erythrocytes.

Experimental evidence has shown that nitrite anion plays a key role in one of the proposed mechanisms for hypoxic vasodilation, in which the erythrocyte acts as a NO generator and deoxygenated hemoglobin in pre-capillary arterioles reduces nitrite to NO, which contributes to vascular smooth muscle relaxation. However, because of the complex reactions among nitrite, hemoglobin, and the NO that is formed, the amount of NO delivered by this mechanism under various conditions has not been quantified experimentally. Furthermore, paracrine NO is scavenged by cell-free hemoglobin, as shown by studies of diseases characterized by extensive hemolysis (e.g., sickle cell disease) and the administration of hemoglobin-based oxygen carriers. Taking into consideration the free access of cell-free hemoglobin to the vascular wall and its ability to act as a nitrite reductase, we have now examined the hypothesis that in hypoxia this cell-free hemoglobin could serve as an additional endocrine source of NO. In this study, we constructed a multicellular model to characterize the amount of NO delivered by the reaction of nitrite with both intraerythrocytic and cell-free hemoglobin, while intentionally neglecting all other possible sources of NO in the vasculature. We also examined the roles of hemoglobin molecules in each compartment as nitrite reductases and NO scavengers using the model. Our calculations show that: (1) approximately 0.04pM NO from erythrocytes could reach the smooth muscle if free diffusion were the sole export mechanism; however, this value could rise to approximately 43pM with a membrane-associated mechanism that facilitated NO release from erythrocytes; the results also strongly depend on the erythrocyte membrane permeability to NO; (2) despite the closer proximity of cell-free hemoglobin to the smooth muscle, cell-free hemoglobin reaction with nitrite generates approximately 0.02pM of free NO that can reach the vascular wall, because of a strong self-capture effect. However, it is worth noting that this value is in the same range as erythrocytic hemoglobin-generated NO that is able to diffuse freely out of the cell, despite the tremendous difference in hemoglobin concentration in both cases (microM hemoglobin in plasma vs. mM in erythrocyte); (3) intraerythrocytic hemoglobin encapsulated by a NO-resistant membrane is the major source of NO from nitrite reduction, and cell-free hemoglobin is a significant scavenger of both paracrine and endocrine NO.     

Nitric oxide irreversibly inhibits cytochrome oxidase at low oxygen concentrations: evidence for inverse oxygen concentration-dependent peroxynitrite formation

The present study shows that nitric oxide (NO) irreversibly inhibits purified cytochrome oxidase in a reverse oxygen concentration-dependent manner. The inhibition is dramatically protected by a peroxynitrite scavenger, suggesting that peroxynitrite is formed from the reaction of NO with cytochrome oxidase at low oxygen concentration, and that peroxynitrite is involved in irreversible cytochrome oxidase inactivation. Production of nitroxyl anion or superoxide was tested as potential mechanisms underlying the conversion of NO to peroxynitrite. A nitroxyl anion scavenger potently protected the irreversible inhibition, whereas a superoxide dismutase did not provide protective effect, suggesting that the peroxynitrite was formed from nitroxyl anion rather than the reaction of NO with superoxide.     

Nitric oxide and oxygen regulate truncated hemoglobin gene expression in Frankia strain CcI3

The Frankia genome contains two truncated hemoglobin genes (hboN and hboO) whose functions remain to be determined. Nitric oxide (NO) generated by the addition of 400 microM SNAP (S-nitroso-N-acetylpenicillamine) caused a 10-fold increase in hboN gene expression but had no effect on hboO expression. The addition of the NO scavenger, carboxy-PT10, reduced the effect of SNAP. hboO gene expression increased under low-oxygen conditions, while hboN expression was unaffected. These results suggest that HboN may function in protection from nitrosative stress and that HboO may act as an oxygen transport molecule for increased respiration in hypoxic environments.     

Scavenging of reactive nitrogen species by oxygenated hemoglobin: globin radicals and nitrotyrosines distinguish nitrite from nitric oxide reaction

The reaction of *NO and NO2- with hemoglobin (Hb) is of pivotal importance to blood vessel function. Both species show at least two different reactions with Fe2+ Hb: one with deoxygenated Hb, in which the biological properties of *NO are preserved, and another with oxygenated hemoglobin (oxyHb), in which both species are oxidizes to NO3-. In this study we compared the oxidative reactions of *NO and NO2- and, in particular, the radical intermediates formed during transformation to NO3-. The reaction of NO2- with oxyHb was accelerated at high heme concentrations and produced stoichiometric amounts of NO3-. Direct EPR and spin trapping studies showed that NO2-, but not *NO, induced the formation of globin Tyr-, Trp-, and Cys-centered radicals. MS studies provided evidence of the formation of approximately 2% nitrotyrosine in both the alpha and beta subunits, suggesting that *NO2 diffuses in part away from the heme and reacts with Tyr radicals. No nitrotyrosines were detected in the reaction of *NO with oxyHb. Collectively, these results indicate that NO2- reaction with oxyHb causes an oxidative challenge not observed with *NO. The differences in oxidation mechanisms of *NO and NO2- are discussed.     

Nitric oxide and hemoglobin interactions in the vasculature.

As an endothelium-derived relaxing factor, nitric oxide (NO) maintains blood flow and O2 transport to tissues. Under normal conditions a delicate balance exists in the vascular system between endothelium-derived NO, an antioxidant, and the pro-oxidant elements of the vascular system, O-2, and peroxynitrite (a by-product of the reaction of NO and superoxide); in addition there is a balance between neurogenic tonic contraction and NO-mediated relaxation. The former balance can be disrupted in favor of peroxynitrite and hydrogen peroxide under the conditions of ischemia/reperfusion. This review suggests that NO may be beneficial, not only in terms of its new potential in improving O2 transport without accompanying significant increase in tissue blood flow, but also in its ability to suppress the prooxidative reagents of the vascular systems. These include NO-mediated inhibition of transendothelial migration by leukocyte and the antioxidative effects of NO with regard to ischemia/reperfusion; the relevance of these hypotheses to systemic administration of NO donors is discussed.     

Iron nitrosyl hemoglobin formation from the reaction of hydroxylamine and hemoglobin under physiological conditions

Sickle cell disease patients receiving hydroxyurea (HU) therapy have shown increases in the production of nitric oxide (NO) metabolites, which include iron nitrosyl hemoglobin (HbNO), nitrite, and nitrate. However, the exact mechanism by which HU forms HbNO in vivo is not understood. Previous studies indicate that the reaction of oxyhemoglobin (oxyHb) or deoxyhemoglobin (deoxyHb) with HU are too slow to account for in vivo HbNO production. In this study, we show that the reaction of methemoglobin (metHb) with HU to form HbNO could potentially be fast enough to account for in vivo HbNO formation but competing reactions of either excess oxyHb or deoxyHb during the reaction reduces the likelihood that HbNO will be produced from the metHb-HU reaction. Using electron paramagnetic resonance (EPR) spectroscopy we have detected measurable amounts of HbNO and metHb during the reactions of oxyHb, deoxyHb, and metHb with excess hydroxylamine (HA). We also demonstrate HbNO and metHb formation from the reactions of excess oxyHb, deoxyHb, or metHb and HA, conditions that are more likely to mimic those in vivo. These results indicate that the reaction of hydroxylamine with hemoglobin produces HbNO and lend chemical support for a potential role for hydroxylamine in the in vivo metabolism of hydroxyurea.     

Nitric oxide-forming reaction between the iron-N-methyl-D-glucamine dithiocarbamate complex and nitrite

The objective of this study was to elucidate the origin of the nitric oxide-forming reactions from nitrite in the presence of the iron-N-methyl-D-glucamine dithiocarbamate complex ((MGD)(2)Fe(2+)). The (MGD)(2)Fe(2+) complex is commonly used in electron paramagnetic resonance (EPR) spectroscopic detection of NO both in vivo and in vitro. Although it is widely believed that only NO can react with (MGD)(2)Fe(2+) complex to form the (MGD)(2)Fe(2+).NO complex, a recent article reported that the (MGD)(2)Fe(2+) complex can react not only with NO, but also with nitrite to produce the characteristic triplet EPR signal of (MGD)(2)Fe(2+).NO (Hiramoto, K., Tomiyama, S., and Kikugawa, K. (1997) Free Radical Res. 27, 505-509). However, no detailed reaction mechanisms were given. Alternatively, nitrite is considered to be a spontaneous NO donor, especially at acidic pH values (Samouilov, A., Kuppusamy, P., and Zweier, J. L. (1998) Arch Biochem. Biophys. 357, 1-7). However, its production of nitric oxide at physiological pH is unclear. In this report, we demonstrate that the (MGD)(2)Fe(2+) complex and nitrite reacted to form NO as follows: 1) (MGD)(2)Fe(2).NO complex was produced at pH 7.4; 2) concomitantly, the (MGD)(3)Fe(3+) complex, which is the oxidized form of (MGD)(2)Fe(2+), was formed; 3) the rate of formation of the (MGD)(2)Fe(2+).NO complex was a function of the concentration of [Fe(2+)](2), [MGD], [H(+)] and [nitrite].     

Formation of intermediate products in the reaction of hemoglobin with cyanide

Interaction between methemoglobin and cyanide was studied by low temperature inhibition method in combination with ESR. A new, not earlier described in literature ESR signal of low spin cyanide complex of this protein was recorded.     

The reaction between nitrite and hemoglobin: the role of nitrite in hemoglobin-mediated hypoxic vasodilation

The reaction between nitrite and hemoglobin has been studied for over a century. However, recent evidence indicating nitrite is a latent vasodilatory agent that can be activated by its reaction with deoxyhemoglobin has led to renewed interest in this reaction. In this review we survey, in the context of our own recent studies, the chemical reactivity of nitrite with oxyhemoglobin, deoxyhemoglobin and methemoglobin, and place these reactions in both a physiological and pharmacological/therapeutic context.     

Nitric oxide scavenging by Mycobacterium leprae GlbO involves the formation of the ferric heme-bound peroxynitrite intermediate

Ferrous oxygenated (Fe(II)O2) hemoglobins (Hb's) and myoglobins (Mb's) have been shown to react very rapidly with NO, yielding NO3(-) and the ferric heme-protein derivative (Fe(III)), by means of the ferric heme-bound peroxynitrite intermediate (Fe(III)OONO), according to the minimum reaction scheme: Fe(II)O2 + NO (k(on))--> Fe(III)OONO (h)--> Fe(III) + NO3(-). For most Hb's and Mb's, the first step (indicated by k(on)) is rate limiting, the overall reaction following a bimolecular behavior. By contrast, the rate of isomerization and dissociation of Fe(III)OONO (indicated by h) is rate limiting in NO scavenging by Fe(II)O2 murine neuroglobin, thus the overall reaction follows a monomolecular behavior. Here, we report the characterization of the NO scavenging reaction by Fe(II)O2 truncated Hb GlbO from Mycobacterium leprae. Values of k(on) (=2.1x10(6) M(-1) s(-1)) and h (=3.4 s(-1)) for NO scavenging by Fe(II)O2 M. leprae GlbO have been determined at pH 7.3 and 20.0 degrees C, the rate of Fe(III)OONO decay (h) is rate limiting. The Fe(III)OONO intermediate has been characterized by optical absorption spectroscopy in the Soret region. These results have been analyzed in parallel with those of monomeric and tetrameric globins as well as of flavoHb and discussed with regard to the three-dimensional structure of mycobacterial truncated Hbs and their proposed role in protection from nitrosative stress.     

Nitric oxide modulates capillary formation at the endothelial cell-tumor cell interface

Nitric oxide synthase expression has been documented in lung tumors, but a potential role for nitric oxide (NO) in induction of capillary formation remains to be elucidated. The purpose of this report was to characterize the direct effects of NO at the level of the tumor-endothelium interface with respect to angiogenesis. A Transwell two-compartment culture system, human endothelial cells (EC), and two human non-small cell lung cancer (CA) lines that constitutively produce NO were used to simulate the EC-tumor cell interface. Both histological types of lung CA, squamous and adenocarcinoma, induced baseline capillary formation by EC within 3 days. This process was inhibited by NO in the microenvironment because decreasing NO production with 100 microM aminoguanidine (AG) significantly increased capillary formation, whereas coincubation with 100 microM AG plus 400 microM L-arginine returned angiogenesis to baseline values. We demonstrate further that NO may exert its inhibitory effects by influencing matrix metalloproteinase expression/activity and tyrosine phosphorylation of proteins in the sprouting tips of nascent capillaries.     

Nitric oxide and nitrite are likely mediators of pollen interactions

The ability of plants to produce nitric oxide (NO) is now well recognised. In plants, NO is involved in the control of organ development and in regulating some of their physiological functions. We have recently shown that pollen generates NO in a constitutive manner and have measured both intra- and extracellular production of this radical. Furthermore, we have shown that nitrite accumulates in the media surrounding the pollen and have suggested that the generation of these signaling molecules may be important for the normal interaction between the pollen grain and the stigma on which it alights. However, pollen grains inevitably come into contact with other tissues, including those of animals and it is likely that the NO produced will influence the behavior of the cells associated with these tissues. Such non-animal-derived, NO-mediated effects on mammalian cells may not be restricted to pollen and plant debris and fungal spore-derived NO may elicit similar effects.Key words: allergy, fungal spores, nitric oxide, nitrite, pollenNitric oxide (NO) has been recognised as a signaling molecule for 20+ years, but its roles in controlling cellular activity are far from fully understood. In plants, NO is involved in numerous biological processes¹ including seed germination,² floral development,³ the control of stomatal closure⁴ and root gravitropism⁵ and is also known to affect gene expression.⁶ Recently, we showed that pollen of Arabidopsis, Senecio and Tradescantia produces NO,⁷ and speculated that its role in this specific context is to help orchestrate early signaling events of the pollen-stigma interaction.^7,8 We subsequently showed that NO generation by pollen is more widespread among angiosperms and not just restricted to the species that were first investigated.⁹ Obviously, this intracellular generation of NO could influence the internal biochemistry of the pollen grain and pollen tube. However, for it to impact on other tissues, such as the stigma, on which the pollen grains alight during pollination, the NO generated would have to be released into the extracellular matrix.To demonstrate that pollen grains do indeed release NO to their surroundings we employed a water soluble derivative of the fluorescent NO probe, diaminofluorescein (DAF), to show that the 525 nm emission of the surrounding solution increased with time and that this fluorescence could be removed by scavenging the NO released from the pollen with compounds such as 2-phenyl-4,4,5,5,-tetramethylimidazoline-1-oxyl 3-oxide (PTIO). Thus, it is quite conceivable that, in vivo, NO produced by pollen moves into the extracellular matrix where it exerts an influence on the activity of cells in the adjacent tissues. Interestingly, in vitro rehydration of the pollen (analagous to the regulated hydration of pollen on the stigma) was needed before NO evolution could be measured. Normally, some form of specific stimulation, such as that which occurs either during pathogenesis¹⁰ or which results from the increased hormone levels observed during stomatal closure,¹¹ is required to initiate NO production by plant tissues. Thus, it is interesting here, that water appears to be the signaling cue to initiate constitutive NO release by the pollen.As a result of its free radical nature, NO is notoriously difficult to measure. As the chemistry involved in their reactivity has become better understood, doubts have been raised concerning the specificity of many of the fluorescent probes that have been used for its detection.¹² Commonly the fluorescent NO probe, DAF, is used, but similar alternative probes such as diamino-rhodamine (DAR) have recently also been described.¹³ Here, Figure 1 shows the NO-dependent fluorescence of DAR4M-AM-infused Brassica napus pollen and the associated temporal increase in the fluorescence of the extracellular medium containing a cell impermeable form of the dye. Despite the use of these different dye-based probes, it has still proved important to use other approaches to detect pollen NO production to refute the possibility that similarly reactive free radicals other than NO are responsible for the increased fluorescence observed. We have, therefore, confirmed our fluorescence measurements using electron paramagnetic resonance (EPR) techniques⁹ which have also indicated the presence of NO. Thus, the use of both fluorescent probe and EPR approaches point to the generation and release of NO from the pollen of all the plant species studied.Open in a separate windowFigure 1The diamino-rhodamine dyes, DAR4M-AM (cell permeable) and DAR4M (cell impermeable), can be used to detect intra- and extracellular pollen-derived nitric oxide (NO) respectively. Aqueous suspensions of Brassica napus sp. pollen were incubated for 15 min at room temp in 10 µM DAR4M-AM either without (A) or with (B) 200 µM of the NO scavenger, 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (cPTIO). In each case, after removal of the excess dye and resuspension of the pollen in 10% (v/v) glycerol, the accumulated DAR4M-AM fluorescence signals within the pollen grains were detected by spinning disc, laser scanning, confocal microscopy with excitation at 560 nm and emission detection at 575 nm. The extracellular accumulation with time of the NO-associated fluorescence signal of the dye, DAR4M, in the media was also followed spectrophotometrically (C). Using the same excitation and emission detection wavelengths, the fluorescence of aqueous suspensions of the pollen in 10 µM DAR4M either without (Ci) or with (Cii) 200 “M cPTIO was monitored over a 10 min. period at room temp. The output fluorescence signal with time is presented in relative units.An additional NO detection technique based on ozone chemiluminescence was also used to confirm the data obtained.⁹ Unlike the fluorescence and EPR approaches which measure the accumulated production of NO, this method detects the steady-state levels of NO at any given time. However, as these levels proved to be very low and not readily detectable by this approach, we altered the assay conditions so as to measure the nitrite that accumulated as a result of NO oxidation in the extracellular media. While the nitrite that accumulated in the media could have done so as a result of being directly excreted by the pollen, the results obtained were in accordance with the earlier observations that pollen evolves NO.⁹ Neither should nitrite be dismissed as a mere downstream by-product. Not only is it the substrate for the production of NO by enzymes such as nitrate reductase,¹⁴ it can also act as a cell signaling molecule in its own right¹⁵ effecting increased cGMP production, increases in different cytochrome P450 activities and the induction of specific gene expression.Having established that pollen produces NO and nitrite, the mechanisms underlying their generation and subsequent signaling require determination. In mammalian cells the production of NO by a family of nitric oxide synthase enzymes is well understood.¹⁶ However, attempts to find plant homologues have so far proved unsuccessful, with the sole proposed candidate¹⁷ having now been shown to be a G protein.^18–20 Nitrate reductase is clearly one source of NO in plants,^11,14 but whether other enzymes exist which are similarly involved remains a matter for debate and discovery. Obviously, as plant NO synthesising enzymes are identified their function in the generation of NO and nitrite in pollen will need to be established.Originally,⁷ we suggested that pollen-derived NO is integral to the pollen-stigma interaction and this now needs to be determined. Nevertheless, the NO and nitrite released externally by pollen may also affect the cells of any moist tissues on which pollen grains land. Such cells may include, for example, those lining mammalian nasal passages. It is well established that NO helps orchestrate the activity of cells involved in human immune responses¹⁶ and this begs the question as to whether or not pollen-produced NO alters these responses during, for example, the onset of the symptoms of hayfever? Many plant cells produce NO, particular during stress and after wounding²¹ and damaged plant tissues that come into contact with human cells in environments that create such debris also have the potential to elicit similar responses. The reaction of mammalian cells to fungi, which are known to possess NOS enzymes²² and whose spores are a main contributor to asthma,²³ may also be similarly mediated.To conclude, pollen grains appear to generate both NO and nitrite constitutively. Determining the functional significance and ramifications of this production in terms of both endogenous and exogenous cell signaling is an important focus for future research.     

Concerted nitric oxide formation and release from the simultaneous reactions of nitrite with deoxy- and oxyhemoglobin

Recent studies reveal a novel role for hemoglobin as an allosterically regulated nitrite reductase that may mediate nitric oxide (NO)-dependent signaling along the physiological oxygen gradient. Nitrite reacts with deoxyhemoglobin in an allosteric reaction that generates NO and oxidizes deoxyhemoglobin to methemoglobin. NO then reacts at a nearly diffusion-limited rate with deoxyhemoglobin to form iron-nitrosyl-hemoglobin, which to date has been considered a highly stable adduct and, thus, not a source of bioavailable NO. However, under physiological conditions of partial oxygen saturation, nitrite will also react with oxyhemoglobin, and although this complex autocatalytic reaction has been studied for a century, the interaction of the oxy- and deoxy-reactions and the effects on NO disposition have never been explored. We have now characterized the kinetics of hemoglobin oxidation and NO generation at a range of oxygen partial pressures and found that the deoxy-reaction runs in parallel with and partially inhibits the oxy-reaction. In fact, intermediates in the oxy-reaction oxidize the heme iron of iron-nitrosyl-hemoglobin, a product of the deoxy-reaction, which releases NO from the iron-nitrosyl. This oxidative denitrosylation is particularly striking during cycles of hemoglobin deoxygenation and oxygenation in the presence of nitrite. These chemistries may contribute to the oxygen-dependent disposition of nitrite in red cells by limiting oxidative inactivation of nitrite by oxyhemoglobin, promoting nitrite reduction to NO by deoxyhemoglobin, and releasing free NO from iron-nitrosyl-hemoglobin.     

Peroxynitrite formation from the simultaneous reduction of nitrite and oxygen by xanthine oxidase

One electron reductions of oxygen and nitrite by xanthine oxidase form peroxynitrite. The nitrite and oxygen reducing activities of xanthine oxidase are regulated by oxygen with K(oxygen) 26 and 100 microM and K(nitrite) 1.0 and 1.1 mM with xanthine and NADH as donor substrates. Optimal peroxynitrite formation occurs at 70 microM oxygen with purine substrates. Kinetic parameters: V(max) approximately 50 nmol/min/mg and K(m) of 22, 36 and 70 microM for hypoxanthine, pterin and nitrite respectively. Peroxynitrite generation is inhibited by allopurinol, superoxide dismutase and diphenylene iodonium. A role for this enzyme activity can be found in the antibacterial activity of milk and circulating xanthine oxidase activity.     

Pentahaem cytochrome c nitrite reductase: reaction with hydroxylamine,a potential reaction intermediate and substrate

The pentahaem enzyme cytochrome c nitrite reductase catalyses the reduction of nitrite to ammonia, a key reaction in the biological nitrogen cycle. The enzyme can also transform nitrogen monoxide and hydroxylamine, two potential bound reaction intermediates, into ammonia. Structural and mechanistic aspects of the multihaem enzyme are discussed in comparison with hydroxylamine oxidoreductase, a trimeric protein with eight haem molecules per subunit.     

Effect of some organic cosolvents on the reaction of hemoglobin with oxygen

We studied the effects of some organic cosolvents (monohydric alcohols and amides) on the reaction of hemoglobin with oxygen. We present evidence showing that our data can be analyzed within the framework of the Monod-Wyman-Changeux model and that the main effect of cosolvents is to alter the T ? R conformational equilibrium of hemoglobin, without significantly affecting the intrinsic oxygen dissociation constants. Following a previously described phenomenological approach, the overall effects have been separated into effects related to the variation of the bulk dielectric constant of the solvent and effects not related to the variation of this constant.