Aromatic residues in the C terminus of apolipoprotein C-III mediate lipid binding and LPL inhibition

Plasma apoC-III levels correlate with triglyceride (TG) levels and are a strong predictor of CVD outcomes. ApoC-III elevates TG in part by inhibiting LPL. ApoC-III likely inhibits LPL by competing for lipid binding. To probe this, we used oil-drop tensiometry to characterize binding of six apoC-III variants to lipid/water interfaces. This technique monitors the dependence of lipid binding on surface pressure, which increases during TG hydrolysis by LPL. ApoC-III adsorption increased surface pressure by upward of 18 mN/m at phospholipid/TG/water interfaces. ApoC-III was retained to high pressures at these interfaces, desorbing at 21–25 mN/m. Point mutants, which substituted alanine for aromatic residues, impaired the lipid binding of apoC-III. Adsorption and retention pressures decreased by 1–6 mN/m in point mutants, with the magnitude determined by the location of alanine substitutions. Trp42 was most critical to mediating lipid binding. These results strongly correlate with our previous results, linking apoC-III point mutants to increased LPL binding and activity at lipid surfaces. We propose that aromatic residues in the C-terminal half of apoC-III mediate binding to TG-rich lipoproteins. Increased apoC-III expression in the hypertriglyceridemic state allows apoC-III to accumulate on lipoproteins and inhibit LPL by preventing binding and/or access to substrate.     

Changes in glycosylation alter the affinity of the human transferrin receptor for its ligand

When transferrin receptors of human erythroleukemic cells were pulse-labeled with [35S]methionine and then chased in the absence of radioactive precursor, the first detectable immunoprecipitable form of the receptor had a molecular mass of 85 kDa. This form of the receptor was converted to the mature form of 93 kDa with a half-time of about 40-60 min. Both the immature (85 kDa) and mature (93 kDa) receptors associated as dimers, the native form of the receptor. The 85-kDa, as well as the 93-kDa, receptors bound to a monoclonal antibody raised against the transferrin receptor or to transferrin-Sepharose. In order to determine whether glycosylation was necessary for ligand binding, purified receptors were isolated from cells grown in the presence of tunicamycin. When K562 cells were grown in the presence of tunicamycin, an 80-kDa nonglycosylated form of the receptor was synthesized. This nonglycosylated receptor was also capable of dimer formation; however, much less of it reached the cell surface than the fully glycosylated form, although both untreated and tunicamycin-grown cells appeared to synthesize transferrin receptors at similar rates. Although the number of receptor molecules/cell was similar in control and tunicamycin-treated cells, the nonglycosylated receptors exhibited a much lower affinity for transferrin than those of untreated cells; in contrast, when receptors were purified by immunoprecipitation and digested with bacterial alkaline phosphatase, no difference was observed between the affinity of these receptors and undigested immunoprecipitated receptors. These results suggest that glycosylation is not necessary for specific binding of transferrin to its receptor, but the affinity of this binding can be influenced greatly by the presence or absence of carbohydrate residues.     

Single amino acid substitutions in the C-terminus of collagen II alter its affinity for collagen IX

The structural integrity of cartilage depends on the presence of extracellular matrices (ECM) formed by heterotypic fibrils composed of collagen II, collagen IX, and collagen XI. The formation of these fibrils depends on the site-specific binding between relatively small regions of interacting collagen molecules. Single amino acid substitutions in collagen II change the physicochemical and structural characteristics of those sites, thereby leading to an alteration of intermolecular collagen II/collagen IX interaction. Employing a biosensor to study interactions between R75C, R789C or G853E collagen II mutants and collagen IX, we demonstrated significant changes in the binding affinities. Moreover, analyses of computer models representing mutation sites defined exact changes in physicochemical characteristics of collagen II mutants. Our study shows that changes in collagen II/collagen IX affinity could represent one of the steps in a cascade of changes occurring in the ECM of cartilage as a result of single amino acid substitutions in collagen II.     

Changes in oxytocin content in the magnocellular neurons of the rat hypothalamus following water deprivation or estrogen treatment

Summary The effect of water deprivation or estrogen treatment on the oxytocin content of rat hypothalamic cells was examined using a quantitative immunohistological technique. Oxytocin-containing cells were visualized using the immunoperoxidase technique of Sternberger and a primary antiserum directed against oxytocin. The optical density of the darkest 3.2 m diameter spot in the cytoplasm of a cell was used as a measure of the oxytocin content of that cell. Water deprivation produced a significant decrease in anti-oxytocin staining in the anterior commissural nucleus of males and females. There was a similar decrease in the paraventricular nucleus of males, but not in the paraventricular nucleus of females or the supraoptic nucleus of either males or females. Estrogen treatment of ovariectomized female rats produced a fall in anti-oxytocin staining in the anterior commissural, but not paraventricular or supraoptic nuclei.     

Changes in continental ostracode shell chemistry; uncertainty of cause

Ostracode shell chemistry is a powerful tool for recording changes of certain dissolved ions in their environment. Such data are commonly interpreted in terms of change in temperature and salinity, which are then used to offer insights into paleohydrology and from that paleoclimate. In particular, the changes in Sr/Ca_shell are believed to reflect changes in salinity, and the changes in Mg/Ca_shell to reflect both salinity and water temperature. However, the established application of this proxy too often ignores the complexities involved in the chemical changes accompanying solute evolution, hydrologic change, physical chemistry, and the autoecology and biology of ostracodes. Chemical changes occur: (1) in the dissolved Mg/Ca and Sr/Ca ratios during solute evolution, (2) as a consequence of multiple sources of water, but especially ground and surface water interchange as well as evaporation, (3) as a consequence of different dissolved cation–anion pair formation at various concentrations, and (4) because of bio/ecologic effects, including seasonality of molting and taxa-specific ionic regulation capabilities. We suggest that changes in shell chemistry in a stratigraphic sequence tell us when changes occurred in the solutes, but cannot identify what caused those change(s) in the chemical environment. Inclusion of information from other paleoenvironmental and paleoclimatic proxies that co-occur with ostracode shells may help to limit the choices amongst possible causes.

Changes in cold hardiness of introduced and native interior Alaskan evergreens in relation to water and lipid content during spring dehardening

Needle hardiness of introduced yellow pine, Pinus banksiana Lamb., lodgepole pine, P. contorta Dougl, and native white spruce, Picea glauca (Moench) Voss, were assessed by the effective prefreezing temperature method. Yellow pine needles were less hardy than lodgepole pine or white spruce needles in Alaska on each date measured. Although hardiness decreased in springtime in all species, decreases in hardiness in yellow pine began before temperatures were above ?20°C, apparently in response to day length, while decreases in hardiness in lodgepole pine and white spruce began only when mean temperatures were above 0°C. Hardiness was increased by decreasing the water content of yellow pine and spruce needles. However, only the latter increased its field hardiness by decreased water contents, and only to a small degree. Large decreases in phospholipid occurred during the dehardening period, indicating the presence of major membrane-associated changes. However, changes in hardiness did not closely parallel those in phospholipid; hardiness decreased before phospholipid did in spruce and after phospholipid did in lodgepole pine. In yellow pine, changes in hardiness were more closely related to changes in phospholipid content. Decreases in phospholipid appeared to be correlated with the day length in all species.     

Changes in needle quality and larch bud moth performance in response to CO2 enrichment and defoliation of treeline larches

Abstract. 1. It is hypothesised that the larch bud moth cycle is controlled by host‐tree foliage quality. In a Free Air CO₂ Enrichment (FACE) experiment at the Swiss alpine treeline (2180 m a.s.l.), the effects of elevated CO₂ and previous year defoliation on needle quality of larch and the performance of the larch bud moth were investigated. 2. Starch and lignin concentrations increased and water content decreased in elevated CO₂‐grown needles compared with ambient CO₂ concentration. Defoliation resulted in reduced N, water, starch, and sugar concentrations in needles of the next year generation. No interactions between elevated CO₂ and defoliation on needle quality were observed. 3. Needle quality changes due to needle maturation over the course of the experiment, however, were much larger than the effects of elevated CO₂ and defoliation. For example, N concentration was on average 38% lower and lignin concentration 55% higher at the end of the experiment (early July 2003) than at the beginning (mid June 2003). 4. On non‐defoliated trees, larch bud moth larvae grew somewhat more slowly under elevated CO₂ compared with ambient CO₂ concentration. If, however, trees had been defoliated, this response was reversed, with a faster growth of larch bud moth on high CO₂‐exposed trees than on control trees. Pupal weight was not affected by either CO₂ treatment or defoliation. 5. These results suggest that the larch bud moth has to cope with large changes in food quality due to needle maturation during its development, and that additional CO₂‐ and defoliation‐induced alterations in needle chemistry have comparatively minor influences on larch bud moth performance at the treeline.     

Superficially active water in lipid membranes and its influence on the interaction of an aqueous soluble protease

The purpose of this paper is to demonstrate that the interaction of an aqueous soluble enzyme with lipid membranes is influenced by the lipid composition of the interphase. The results show that the interaction of an aqueous soluble protease, Rennet from Mucor miehei, depends on the exposure of the carbonyl and phosphate groups at the membrane interphase. The changes produced by the protease on the surface pressure of monolayers of dimyristoylphosphatidylcholine (DMPC); dioleoylphosphatidylcholine (DOPC); diphytanoylphosphatidylcholine (DPhPC); dipalmitoylphosphatidylcholine (DPPC); di-O-tetradecylphosphatidyl-choline [D(ether)PC]; dimyristoylphosphatidylethanolamine (DMPE); di-O-tetradecyl-phosphatidylethanolamine [D(ether)PE] were measured at different initial surface pressures. The meaning of the ΔΠ vs. Π curves was interpreted in the light of the concept of interphase given by Defay and Prigogine [R. Defay, I. Prigogine, Surface Tension and Adsorption, John Wiley & Sons, New York, 1966, pp. 273-277] considering the interphase as a bidimensional solution of polar head groups. With this approach, and based on reported evidences that carbonyls and phosphates are the main hydration sites of the lipid membranes, it is suggested that the mechanism of interaction of aqueous soluble protein involves water beyond the hydration shell. At high surface pressure, only water strongly bound to carbonyl and phosphate groups is present and the interaction is not occurring. In contrast, at low surface pressures, the protease-membrane interaction is a function of acyl chain for different polar groups. This is interpreted, as a consequence of the changes in the interfacial tension produced by the displacement of water confined between the hydrated head groups.     

The effect of amine structure on complexation with lasalocid in model membrane systems. II. Ionophore selectivity for amines in lipid bilayers and at oil/water interfaces

The ionophore antibiotic X-537A (lasalocid) transports biogenic amines across biological and artificial membranes. The major portion of amine flux (greater than 99%) occurs as a 1:1 neutral complex. The rank order of ionophore selectivity was determined for lipid bilayer membrane transport of amines based on a comparison of permeability coefficients: p-tyramine ～ β-phenylethylamine ～ amphetamine > methamphetamine > dopamine > phenylephrine ～ metanephrine > norepinephrine > epinephrine. This rank order is in agreement with results obtained from partitioning measurements which were carried out in parallel to the bilayer membrane experiments. A correlation between amine structure and binding characteristics has been developed.     

Effects of hydrologic changes on aboveground production and surface water chemistry in two boreal peatlands in Alberta: Implications for global warming

Aboveground net primary production (NPP) and surface water chemistryvariables were monitored in a lacustrine sedge fen and a bog for four years.There were no significant differences in precipitation, mean growing seasonannual temperature, and number of growing degree days from 1991 to 1994. Themean annual water levels in the lacustrine sedge fen differed significantly,whereas they were similar in the bog during these four years. We measured 15surface water variables in the lacustrine sedge fen and the bog, and foundthat only two correlated significantly with water level fluctuations. In thelacustrine sedge fen, calcium correlated positively (r²= 0.56) and nitrate correlated negatively (r² =0.20) with water levels. In the bog, potassium correlated positively(r² = 0.88) and total dissolved phosphorus correlatednegatively (r² = 0.62) with water levels. The remainingchemical variables showed no significant correlations with water levelfluctuations. Net primary production of the different vegetation strataappeared to respond to different environmental variables. In the lacustrinesedge fen, graminoid production was explained to a significant degree bywater levels (r² = 0.53), whereas shrub production wasexplained to a significant degree by surface water chemistry variables, suchas nitrate (r² = 0.74) and total phosphorus(r² = 0.22). In the bog, temperature was the onlyvariable that explained moss production to a significant degree(r² = 0.71), whereas ammonium explained graminoidproduction (r² = 0.66) and soluble reactive phosphorusexplained shrub production to significant degrees (r² =0.71). There are few direct data on the impact of climatic warming in borealwetlands, although paleoecological and 2×CO₂ model datahave provided some indications of past and possibly future changes invegetation composition, respectively. Our results suggest that thelacustrine sedge fen may succeed to a bog dominated by Sphagnum spp. andPicea mariana, whereas the bog may succeed to an upland-type forestecosystem. This revised version was published online in July 2006 with corrections to the Cover Date.     

Changes in lipid peroxidation, superoxide dismutase activity, ascorbic acid and phospholipid content in liver of freshwater catfish Heteropneustes fossilis exposed to elevated temperature

1. 1. Lipid peroxidation, superoxide dismutase (SOD) activity, ascorbic acid (AsA) and individual phospholipid contents in liver of fresh water cat fish Heteropneustes fossilis were measured after exposure to different temperatures (25, 27, 32, 37°C) at various times (1–4 h).

2. 2. Lipid peroxidation and superoxide dismutase activity were significantly increased with increases in temperature at various times.

3. 3. Ascorbic acid content was depleted when temperature was increased.

4. 4. After temperature exposure, phosphatidyl inositol was increased while phosphatidyl choline, phosphatidyl serine and phosphatidyl ethanolamine were depleted. Phosphatidic acid level did not change.

5. 5. The findings indicated an increased oxidative stress in liver following increases in temperature at various times. Concurrent with the increase in lipid peroxidation, superoxide dismutase activity and ascorbic acid from the liver of fish varied. It is suggested that depletion of major individual phospholipids following temperature exposure could be due to superoxide created oxidative stress in the liver.

     

Free energy of helical transmembrane peptide dimerization in OPLS-AA/Berger force field simulations: inaccuracy and implications for partner-specific Lennard-Jones parameters between peptides and lipids

Interactions between transmembrane (TM) peptides are important in biophysical chemistry, but there are few studies assessing atomistic simulation parameters concerning the energetics of interactions of TM helical peptides. Our potential of mean force analysis using OPLS-AA protein/Berger lipid force fields (FFs) shows that the dimerisation energy of (AALALAA)₃ helical peptides in the dioleoylphosphatidylcholine bilayer is ?4.4 kJ/mol, which was much smaller than the reported experimental value (?12.7 kJ/mol), thus calling for improvement of parameters of the combined FFs. As each of the FFs has been independently developed, we then tested the effects of downscaling the Lennard-Jones (LJ) energy terms between the OPLS-AA atoms and Berger lipid atoms, preserving the parameters within each FF. A 0.9-fold rescaling of the LJ energies was found to render the dimerisation energy close to the experimental value. Solvation of backbone atoms as well as side chain atoms in lipids is crucial for the TM helix interaction. In similar analyses, GROMOS 53A6 FF exhibited as weak dimerisation propensity (~?5.2 kJ/mol) as OPLS-AA/Berger, but CHARMM36 showed relatively accurate propensity (~?9.9 kJ/mol). Challenges and strategies in rendering the TM interaction energy realistic within the framework of current FFs are discussed.     

“Density equilibrium” method for the quantitative and rapid in situ determination of lipid,hydrocarbon, or biopolymer content in microorganisms

The work provides a simple method, based on a direct density equilibrium measurement, for the rapid in situ estimation of total lipid, hydrocarbon or biopolymer content in a variety of prokaryotic and eukaryotic samples. The method can be readily applied to live microalgae and photosynthetic bacteria, single‐celled or colonial microorganisms, as well as cellular fractions and isolated subcellular compartments or components. In this approach, the absolute lipid, hydrocarbon, or biopolymer content of the cells can be readily calculated. This method is especially useful for tracking the oil or polymer content of strains of microalgae and other microorganisms, whose lipid, hydrocarbon or biopolymer content may change with cultivation conditions and/or time, as the case would be in microorganism lipid‐induction industrial processes. The method is also useful for the direct in situ measurement of storage polymer accumulation in live cells, such as starch in microalgae and polyhydroxybutyrate, or other polyhydroxyalkanoates, in photosynthetic and non‐photosynthetic bacteria. Biotechnol. Bioeng. 2009;102: 1406–1415. © 2008 Wiley Periodicals, Inc.     

海南西部桉树人工林土壤水分变化特征及其对林龄的响应

在海南西部儋州林场选取空间相邻、自然环境相似、不同林龄与连栽代次的桉树林样地和椰树林对照样地,通过2010—2012年连续3a定点取样,研究桉树林土壤水分变化特征及其对林龄的响应,分析桉树林种植对林地土壤水分的影响。结果表明:(1)1—4月土壤含水量持续减少,5—6月波动较大,7—10月增加到年内极大值,11—12月降低,但处于年内较高水平。(2)短伐桉树林(二代5年桉树林、三代1年桉树林、三代4年桉树林)、20a桉树林以及10a椰树林5个样地的月均土壤含水量存在显著或极显著差异。二代5年桉树林与三代1年桉树林之间以及20a桉树林与10a椰树林之间的土壤含水量差异均不显著;其余各林地之间土壤含水量差异显著或极显著。(3)随着土壤深度增加,短伐桉树林与20a桉树林、10a椰树林之间的土壤含水量差异增大。表层0—30 cm短伐桉树林年均土壤含水量为6.08%,20a桉树林为7.53%,10a椰树林为6.93%;80 cm以下则分别为8.10%、11.72%和11.95%。与10a椰树林、20a桉树林相比,短伐桉树林对土壤深层水分有较大负面影响。(4)短伐桉树林、20a桉树林和10a椰树林土壤含水量的变异系数由表层到深层逐渐递减,其中林龄较大的短伐桉树林变异系数较大,且变异系数较大的土层也较深厚。与20a桉树林、10a椰树林相比,林龄较大的短伐桉树林对深层土壤水分的消耗较多。(5)连栽代次愈多,林龄越大,土壤含水量愈少;采伐之后1a桉树林的土壤含水量明显增加,有利于桉树后期生长。     

Structural basis for extremely strong binding affinity of giant ankyrins to LC3/GABARAP and its application in the inhibition of autophagy

The Atg8/LC3/GABARAP family of proteins binds its physiological binding partners, which function in macroautophagy (hereafter autophagy), via recognition of their short linear motif, also known as the LC3-interactiong region (LIR) or Atg8-interacting motif (AIM). The AIM/LIR motif, with the consensus sequence [W/F/Y]xx[L/I/V], utilizes the aromatic and hydrophobic residues that bind on the surface of Atg8/LC3/GABARAP. Despite modest binding affinity, this interaction is essential for efficient autophagy. Here we highlight the recent paper by Li and collaborators who discovered the structural basis for a much stronger interaction between the LIR motif-containing peptides and LC3/GABARAP. Moreover, they showed that these peptides are potent and selective inhibitors of autophagy in cultured cells and in C. elegans.     

Changes in pattern and accessibility for 125I-labelling of cell-surface proteins after mesenchymal differentiation of embryonal carcinoma cells

Cell-surface proteins of the embryonal carcinoma line C17-S1 1003 (1003) and of some of its mesenchymal derivatives were studied. The surface proteins were labelled with ¹²⁵I using the lactoperoxidase-glucose-glucose oxidase system either on the cells attached to the culture dishes or after their dissociation. Iodinated proteins were analyzed by two-dimensional gel electrophoresis. The patterns obtained with embryonal carcinoma cells 1003 and with two mesenchymal cell types derived from them, namely embryonic mesenchymal cells (line 10035) and fibroblastic cells (line 10031), were different one from the other, especially when considering the group of proteins labelled on the attached cells. The pattern of cell-surface proteins of the myoblastic line 1168, also derived from C17-S1, was found to be similar to that of 10031 fibroblastic cells. This result is discussed in the light of the phenotypic transition toward myogenesis, which can be obtained with 10031 fibroblastic cells but not with 10035 embryonic mesenchymal cells. A direct method of detection of lectin-binding proteins permitted us to identify the major concanavalin A-binding proteins. Two of them are common to all cell lines studied. They were labeled with ¹²⁵I on the attached undifferentiated 1003 cells, while in all differentiated derivatives they became available for labelling after the cell detachment only.     

Ecological study of Stephanodiscus rotula during a spring diatom bloom: dynamics of intracellular elemental concentrations and correlations in relation to water chemistry, and implications for overall geochemical cycling in a temperate lake

The population of Stephanodiscus rotula in Rostherne Mere (Cheshire, UK) was studied during the spring of 1996 using light microscopy, hydrochemical analyses and scanning electron microscopy X-ray microanalysis (SEM XRMA). Data obtained were statistically analysed to reveal relationships between the elements within the cells and in the lake water. The results confirmed that algal biomass production was mainly controlled by availability of Si. The depletion of ambient Si coincided with changes in the intracellular elemental composition, particularly a considerable reduction of intracellular Si whose depletion was also reflected in changes of intracellular elemental correlations and ratios. A simple structural model of elemental relationships in S. rotula cells is proposed to explain the pattern of intracellular elemental associations. This model can be used as a reference for species response to changes in environmental parameters. S. rotula provided a significant contribution to overall biogeochemical cycling due to the removal of nutrients from the water column and transporting them to bottom sediments following the culmination of the bloom. The role of S. rotula was particularly prominent in the biogeochemical cycle of silicon, as the diatom’s spring growth may account for more than 20% of its total annual loss to bottom sediments.     

H+ Fluxes at Plasmalemma Level: In Vivo Evidence for a Significant Contribution of the Ca2+-ATPase and for the Involvement of its Activity in the Abscisic Acid-Induced Changes in Egeria Densa Leaves

Abstract: The features of Ca²⁺ fluxes, the importance of the Ca²⁺ pump‐mediated H⁺/Ca²⁺ exchanges at plasmalemma level, and the possible involvement of Ca²⁺‐ATPase activity in ABA‐induced changes of H⁺ fluxes were studied in Egeria densa leaves. The results presented show that, while in basal conditions no net Ca²⁺ flux was evident, a conspicuous Ca²⁺ influx (about 1.1 ìmol g^?1 FW h^?1) occurred. The concomitant efflux of Ca²⁺ was markedly reduced by treatment with 5 íM eosin Y (EY), a specific inhibitor of the Ca²⁺‐ATPase, that completely blocked the transport of Ca²⁺ after the first 20 ‐ 30 min. The decrease in Ca²⁺ efflux induced by EY was associated with a significant increase in net H⁺ extrusion (?ÄH⁺) and a small but significant cytoplasmic alkalinization. The shift of external [Ca²⁺] from 0.3 to 0.2 mM (reducing Ca²⁺ uptake by about 30 %) and the hindrance of Ca²⁺ influx by La³⁺ were accompanied by progressively higher ?ÄH⁺ increases, in agreement with a gradual decrease in the activity of a mechanism counteracting the Ca²⁺ influx by an nH⁺/Ca²⁺ exchange. The ABA‐induced decreases in ?ÄH⁺ and pH_cyt were accompanied by a significant increase in Ca²⁺ efflux, all these effects being almost completely suppressed by EY, in line with the view that the ABA effects on H⁺ fluxes are due to activation of the plasmalemma Ca²⁺‐ATPase. These results substantially stress the high sensitivity and efficacy of the plasmalemma Ca²⁺ pump in removing from the cytoplasm the Ca²⁺ taken up, and the importance of the contribution of Ca²⁺ pump‐mediated H⁺/Ca²⁺ fluxes in bringing about global changes of H⁺ fluxes at plasmalemma level.     

An evaluation of lipid metabolism in the insect trypanosomatid Herpetomonas muscarum uncovers a pathway for the uptake of extracellular insect lipoproteins

Lipid uptake and metabolism by trypanosomatid parasites from vertebrate host blood have been well established in the literature. However, there is a lack of knowledge regarding the same aspects concerning the parasites that cross the hemolymph of their invertebrate hosts. We have investigated the lipid composition and metabolism of the insect trypanosomatid Herpetomonas muscarum by ³H- palmitic acid and phosphate (³²Pi) and the parasite interaction with Lipophorin (Lp) the main lipid carrying protein of insect hemolymph. Gas chromatography-mass spectrometry (GC–MS) analyses were used to identify the fatty acids and sterols composition of H.muscarum. Furthermore, we investigated the Lp binding site in the plasma membrane of parasite by Immunolocalization. We showed that H. muscarum incorporated 3H-palmitic acid and inorganic phosphate (32Pi) which were readily used as precursor molecules of lipid biosynthetic pathways. Furthermore, H. muscarum was able to take up both protein and lipid moieties of Lp which could be used as nutrient sources. Moreover, we have also demonstrated for the first time the presence of a Lp binding site in the membrane of a parasite. Such results point out the role of describing the metabolic pathways of trypanosomatids in order to provide a better understanding of parasite-host interaction peculiarities. Such studies may enhance the potential form the identification of novel chemotherapeutic targets in harmful parasites.