One of the main challenges in toxicology today is to develop therapeutic alternatives for the treatment of snake venom injuries that are not efficiently neutralized by conventional serum therapy. Venom phospholipases A2 (PLA2s) and PLA2-like proteins play a fundamental role in skeletal muscle necrosis, which can result in permanent sequelae and disability. This leads to economic and social problems, especially in developing countries. In this work, we performed structural and functional studies with Piratoxin-I, a Lys49-PLA2 from Bothropspirajai venom, complexed with two compounds present in several plants used in folk medicine against snakebites. These ligands partially neutralized the myotoxic activity of PrTX-I towards binding on the two independent sites of interaction between Lys49-PLA2 and muscle membrane. Our results corroborate the previously proposed mechanism of action of PLA2s-like and provide insights for the design of structure-based inhibitors that could prevent the permanent injuries caused by these proteins in snakebite victims.
Citation: Fernandes CAH, Cardoso FF, Cavalcante WGL, Soares AM, Dal-Pai M, Gallacci M, et al. (2015) Structural Basis for the Inhibition of a Phospholipase A2-Like Toxin by Caffeic and Aristolochic Acids. PLoS ONE 10(7): e0133370. doi:10.1371/journal.pone.0133370
Editor: Israel Silman, Weizmann Institute of Science, ISRAEL
Received: May 30, 2015; Accepted: June 25, 2015; Published: July 20, 2015
Copyright: © 2015 Fernandes et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: The coordinates were deposited in the Protein Data Bank (PDB) under the identification codes 4YZ7 (PrTX-I/AA) and 4YU7(PrTX-I/CA).
Funding: Support was provided by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) to CAHF, FFC, WGLC, MDP, MRMF; Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) to MDP, AMS, MRMF and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) to MRMF.
Competing interests: The authors have declared that no competing interests exist.
In Asia, Africa and Latin America,approximately 98% of the world’s snakebites occur, with 421,000 envenomations and 20,000 deaths by ophidian accidents . However, these numbers may be as high as 1,841,000 envenomations and 94,000 deaths per year, considering the under-reporting that occurs in these regions . The mortality caused by snakebites ishigher thanseveral neglected tropical diseases, including dengue hemorrhagic fever, leishmaniasis, cholera, schistosomiasis and Chagas disease . Consequently, the World Health Organization (WHO) recognizes snakebites as an important neglected tropical disease.
In Latin America, snakes of the Bothropsgenusare responsible for approximately 80% of all ophidian accidents[3,4]. Envenomation by these snakes is associated with prominent local tissue damage characterized by swelling, blistering, hemorrhaging and necrosis of the skeletal muscle. These effects are not efficiently neutralized by conventional serum therapy and can result in permanent sequelaeand disability[5,6]. The main toxins involved in tissue-damaging activities are the phospholipases A2(PLA2s)and metalloproteinases, which are the most abundant components of venoms from the Bothropsgenus. A subgroup of PLA2s, known as PLA2-like proteins,is catalytically inactive due to lack of Ca2+ coordination related to natural mutationsof its primary structure; however, it is still able to induce a drastic local myonecrosis[8–10]. The most studied PLA2-like proteins are the Lys49-PLA2s, in which the mutations Asp49→Lys and Tyr28→Asn impair the Ca2+ coordination[11,12]. Several studies with Lys49-PLA2s have shown that segment 115–129 of the C-terminal region, which includes a variable combination of positively charged and hydrophobic residues, is responsible for the myotoxic activity of these proteins[13–16]. Recently, a mechanism of action has been proposed for the Lys49-PLA2s and all other PLA2-like proteins that includes a quaternary conformational change for the activation of these proteins and the participation of two independent interaction sites with the membrane [17,18].
In folk medicine, especially in developing countries, several vegetal species are employed for the treatment of ophidian envenomations incommunities that lack prompt access to serum therapy [19,20]. In recent years, some studieshave investigated the effects of plants on snakebites, includingthe isolation and characterization of their active constituents and theelucidation of their possible mechanisms of action [19,21–23].
Aristolochicacid (AA) and caffeic acid (CA) are plant compounds with anti-snake venom properties that are used in folk medicine [19–21]. AA (8-methoxy-6-nitrophenanthro (3,4-d-1,3-dioxole-5-carboxylic acid) is an alkaloid found in several Aristolochia species. This plant is among the most popular anti-snake venom folk compoundsable to neutralize rattlesnake venomactivity. AA causes a dose-dependent inhibition of in vitro phospholipid hydrolysis by human synovial fluid PLA2 and snake venomPLA2s [24–27]. CA (3-(3,4-dihydroxyphenyl 2-propenoic acid) is a cinnamic acid derivative, abundant in nature and with exceptional biochemical reactivity. It has a large variety of potential pharmacological effects, such as anti-oxidant, anti-cancer and anti-viral activities [28–30]. CA is found in Vernoniacondensate leaves, showing antidote activity against Bothropsjararacavenom [19,21]. Additionally, crystalline CA derivatives have been demonstrated to be an antidote against snake venom by oral or parenteral administration .
In this work, we report functional (neuromuscular-blocking and muscle-damage activities) and crystallographicexperiments aimingto studythe possible inhibitory effects of AA and CA onPrTX-I, a Lys49-PLA2 isolated from Bothropspirajai snake venom. Our functional studies indicate that these ligands neutralize the myotoxic activity of PrTX-I but do not present effect on the inhibition of neuromuscular blocking activity. The structural studies demonstrated that both ligands interact withPrTX-I in different regions,corroboratingthe previously proposed myotoxic mechanism for PLA2-like proteins.
Material and Methods
Protein Purification and Inhibitor Source
PrTX-I was isolated from Bothropspirajai snake venom by gelfiltration and ion exchange chromatography techniques, as previously described . Aristolochicacid (AA) and caffeicacid (CA) were purchased from Sigma-Aldrich (St Louis, MO, USA).
Institutional Animal Care and Use Committee (Institute of Biosciences–Sao Paulo State University–UNESP) approved this study under the number 033/05. Animal procedures were in accordance with the guidelines for animal care prepared by the Committee on Care and Use of Labor. Adult male mice weighing 25–30g were maintainedunder a 12 h light-dark cyclein atemperature-controlled environment (22±2°C) for at least 10 daysprior to the experiments, with food and water ad libitum.
Mice were euthanizedby cervical dislocation followed by exsanguination. The phrenic nerve-diaphragm muscle preparation was removed and mounted vertically in a conventional isolated organ-bath chamber containing 15 mL of Ringer’s physiological solution of the following composition (mM): NaCl, 135; KCl, 5; MgCl2, 1; CaCl2, 2; NaHCO3, 15; Na2HPO4, 1; glucose, 11. This solution was bubbled with carbogen (95% O2 and 5% CO2). The preparation was attached to an isometric force transducer (Grass, FT03) to record the twitch tension. The transducer signal output was amplified and recorded on a computer via a transducer signal conditioner (Gould, 13-6615-50) with an AcquireLab Data Acquisition System (Gould). The resting tension was 5 g. Indirect contractions were evoked by supramaximal pulses (0.2 Hz, 0.5 ms) delivered from an electronic stimulator (Grass, S88K) and applied to the phrenic nerve by means of a suction electrode.
The preparation was stabilized for 45 minutes before the addition of a single concentration of toxin. For inhibition experiments, a fixed amount of PrTX-I dissolved in Ringer’s physiological solution was mixed with AA and CAto obtain a 1:1 and 1:5 (w/w) toxin/inhibitor ratio. At molar ratio terms, it means 1:40 and 1:76 for 1:1 (w/w) toxin/inhibitor ratio for AA and CA, respectively, and 1:200 and 1:380 for 1:5 (w/w) ratio. The mixtures were incubated for 30 minutes at 35±2°C. The control experiments were performed in the absence of toxin or in the presence of inhibitors alone. The degree of protection offered by AA and CA after 90 minutes of contact with the preparation was expressed as a percentage of neuromuscular blockade observed in the presence of the mixture of toxin plus inhibitor relative to the blockade observed in the presence of toxin alone.
After the myographicstudy, the diaphragm muscle was removed from the bath and immersed in Bouin’s fixative, and then processed and embedded in Historesin (Kit Historesin Leica). Histological transverse sections (5 mm thick) were cut out in a microtome and stained with hematoxylin and eosin (HE) prior to examination by light microscopy . Morphological damage was quantified in HE-stained preparations using an Imaging Analysis System (Leica, Qwin). The number of fibers with lesions was expressed as a percentage of the total number of cells (muscle damage index) in three non-overlapping non-adjacent areas of each muscle observed at the same magnification. The degree of neutralization offered by AA and CA was expressed as a percentage of the muscle damage index in the presence of the toxin plus inhibitor relative to that index in the presence of the toxin alone.
The data are expressed as the mean ± S.E.M. The statistical analysis of the data was carried out using ANOVA complemented by the Tukey-Kramer test. Values of P<0.05 were considered significant.
Crystallization of the complexes PrTX-I/AA and PrTX-I/CA.
Co-crystallization experiments were performed with PrTX-I at a concentration of 12 mg.mL-1. Crystals of the complexes were obtained by the hanging drop method . AA and CA were dissolved in ultrapure water or 50% (w/v) ethanol, respectively, to give an 8:1 molar ratio of inhibitor:protein in the crystallization drops. The drops consisted of 1 μLprotein solution, 0.2 μLinhibitorsolution and 0.8 μL reservoir solution and were equilibrated against 500 μL of the same reservoir solution. The best crystals were obtained after an optimization process for the native protein crystallization conditions ;the reservoir solution consisted of 26–30% polyethylene glycol 4000 (PEG 4000), 100 mMTris-HCl pH 8.1–8.5 and 200 mM lithium sulfate, as previously described for the PrTX-I/CA complex . Crystals were grown at 291 K for approximately four weeks for both protein complexes.
X-ray data collection and processing.
The X-ray diffraction data for all crystals were collected at a wavelength of 1.45 Å using a synchrotron-radiation source (MX2 station, Laboratório Nacional de Luz Síncrotron, LNLS, Campinas, Brazil) and a MAR CCD imaging-plate detector (MAR Research). Crystals were mounted in nylon loops and flash-cooled in a stream of nitrogen gas at 100 K using no cryoprotectant. The data were processed using the HKL program package .
Structure determination and refinement.
The crystal structures were determined by molecular replacement techniques implemented in the program MOLREP  from the CCP4i program package  using the coordinates fromthe crystal structures of thePrTX-Icomplexed with α-tocopherol (PDB ID 3CYL)and bothropstoxin-I (BthTX-I), and a Lys49-PLA2 isolated from Bothropsjararacussuvenom complexed with PEG 4000 (PDB ID 3IQ3) as models forthe PrTX-I/AAandPrTX-I/CA complexes, respectively. The modeling processes were always performed by manual rebuilding with the program Cootusingelectron density maps calculated with the coefficients 2|Fobs|-|Fcalc|. The models were improved, as judged by the free R-factor , through rounds of crystallographic refinement (positional and restrained isotropic individual B-factor refinement, with an overall anisotropic temperature factor and bulk solvent correction) usingPHENIX. In the structure of the PrTX-I/AA complex, due to a lack of electron density, part or full side chains of the following residues were excluded: Leu2 (monomer A), Phe3 (monomers A and B), Lys7(A,B), Lys11(A), Lys15 (A,B), Lys20(A), Val31(A), Leu32(A,B), Lys36(A,B), Arg43(A), Lys53(A,B), Lys57(A,B), Lys69(A,B), Lys70(A,B), Arg72(A,B), Lys78(A,B), Asp79(A), Asn88(A), Glu94(B), Lys115(A), Lys116(A), Lys122(A), Phe125 (A,B), Lys127(A,B), Lys129(B), and Asp130(A). In the structure of the PrTX-I/CA complex, part or full side chains of the following residues were excluded: Phe3(A), Leu32(B), Lys36(A), Lys53(B), Lys57(A,B), Thr59(A), Lys69(A,B), Lys70(A,B), Lys78(A), Lys127(B), and Lys129(A). Thestereochemicalqualities of the models weredetermined with the PHENIX and MolProbity programs[42,43].
Neuromuscular blocking activity
PrTX-I (1.0 μM) promoted a time-dependent blockade of indirectly evoked twitches in mice phrenic-diaphragm preparations. After 90 minutes, the twitch amplitudes were reduced to 89.4% (Fig 1). The paralyzing effect of PrTX-I could not be reversed by washing the preparation for at least 30 minutes with toxin-free physiological solution (data not shown). The mean time required to reduce the twitch amplitudes by 50% (T½) was 34.0 ± 2.4 minutes. Pre-incubation with CA (1:1 and 1:5 w/w) or AA (1:1 and 1:5 w/w) did not prevent the neuromuscular blockade induced by PrTX-I (Fig 1A and 1B). Alone, CA did not affect the twitch amplitude(Fig 1A),whileAA(68.5 μg/mL) promoted a facilitator effect (Fig 1B).
The ordinate represents the percentage amplitude of twitches relative to the initial amplitude. The abscissa indicates the time from the beginning of each treatment in the organ bath. The points are the mean ± S.E. * indicates the point at which differences between PrTX-I treatments (alone and pre-incubated with CA and AA) and the control become significant. ** indicates the point at which differences between AA (68.5 μg/mL) and the control become significant.
Light microscopy showed that control and CA or AA-treated muscles were of normal appearance. Fibers were delimited by a thin layer of connective tissue (endomysium) and presented a polygonal shape, with an acidophilic sarcoplasmand peripheral nuclei(Fig 2A, 2C, 2E, 2G and 2I). A few fibers from muscles exposed to AA (13.7 μg/mL and 68.5 μg/mL) revealed a loss of myofibrils (Fig 2G and 2I). However, as shown in Fig 3, only muscles exposed to AA (68.5 μg/mL)had a significantmuscle damage index compared to the control (6.8 ± 2.9%, n = 3vs.1.2 ± 0.1%, n = 4). After 90 minutes of contact with PrTX-I, the diaphragm muscle showed several changes, such as round fibers and edema. Many fibers presented cytoplasm areas devoid of myofibrils, some with a central nucleus(Fig 2B). The muscle damage index for the PrTX-I group was significantly higher than the control (35.1 ± 0.7%, n = 4vs1.2 ± 0.1%, n = 4)(Fig 3). In contrast, pre-incubation with CA (13.7 μg/mL and 68.5 μg/mL) or AA (13.7μg/mL) reduced the myotoxic effects of PrTX-I. In fact, diaphragm muscles exposed to the pre-incubation product presented a more conserved aspect (Fig 2D, 2F and 2H). The muscle damage indices of these preparations were 22.0 ± 3.5% and 12.7 ± 1.9% (PrTX-I/CA at ratios of 1:1 and 1:5, respectively) and 20.2 ± 0.9% (PrTX-I/AA at 1:1) (Fig 3). On the other hand, the pre-incubation of AA with PrTX-I at the ratio 1:5 (w/w) did not reduce the muscle damage index when compared to PrTX-I alone (33.8 ± 0.7%, n = 3vs. 35.1 ± 0.7, n = 4) (Fig 2J).
Control muscle (A) and muscle exposed to caffeicacid (CA) and aristolochic acid (AA) (C, E, G and I) show fibers with normal appearance as evidenced by the polygonal aspect of fibers (PF) and endomysium (EN). A few fibers present loss of myofibrils in the muscle exposed to AA (G and I). (B) Muscle exposed to PrTX-I: edema (ED), round fibers (RF), some of which present loss of myofibrils (LM). (D, F, H and J) Muscle exposed to PrTX-I pre-incubated with CA and AA: The fibers have characteristics observed less frequently in the fibers treated with the PrTX-I alone, except in J, which occurred at similar frequencies.
The ordinate represents the percentage of damaged fibers relative to normal fibers and the abscissa indicates the experimental groups. The bars are expressed as the mean ± S.E. * indicates when differences between PrTX-I treatments (alone and pre-incubated with CA or AA) and their respective controls was significant. # indicates when there were significant differences between PrTX-I pre-incubated with inhibitors and PrTX-I alone treatments. + indicates significant differences between PrTX-I treatments pre-incubated with CA. ° indicates significant differences between the AA (68.5 μg/mL) treatment and the Control group.
Overall crystallographic structures
Crystals of both complexesdiffracted at high resolution (Table 1) and classified as belonging to the P21212or P21 space groups for PrTX-I/AA and PrTX-I/CA, respectively. The refinements converged to final R values of 17.3% (Rfree = 23.5%) and 18.3% (Rfree = 22.9%), respectively, for PrTX-I/AA and PrTX-I/CA. The final models (Fig 4) are of a stereochemical quality expected for structures with the same resolution, as indicated by r.m.s.d bonds, r.m.s.d. angles and Ramachandran plot analyses (Table 1). Both structures have seven disulfide bridges in each monomer with the following structural features: (i) an N-terminal α-helix; (ii) a “short” helix; (iii) a Ca2+ binding loop; (iv) two anti-parallel α-helices (2 and 3); (v) two short strands of an anti-parallel β-sheet (β-wing); and (vi) a C-terminal loop (Fig 4), similar to all other class II PLA2s [44,45].
PEG molecules, sulfate ions,AA and CAare indicatedby sticks (in cyan, yellow, blue and green, respectively). In yellow sticks are also highlighted the aminoacids that compose MDiS (Leu121)andMDoS (Lys20, Lys155, Arg118) regions, which interact with AA and CA, respectively. (C) Cα superposition of apo-PrTX-I, PrTX-I/AA, PrTX-I/CA and PrTX-I complexed to rosmarinic acid (PrTX-I/RA) (monomers A and B, respectively) highlighting the most important structural deviations between them.
The inspection of the 2ǀFobsǀ-ǀFcalcǀ electronic density mapof the PrTX-I/CA structure revealed the presence of four CA molecules establishing hydrogen bonds in monomer A with Lys15 and Arg118 and by water molecules with Ile82 and Lys100 (Fig 5). In monomer B, CA molecules establish hydrogen bonds with Lys20 and Arg118 by water molecules with Gly15, Asn17 and Ser21 (Fig 5). Moreover, CA molecules establish hydrophobic contacts with Lys20, Lys115, Ile104, Arg107, Glu108 and Leu121 in monomer A and with Lys15, Lys20 and Lys115 in monomer B (Fig 6). In other Lys49-PLA2s crystal structures, sulfate ions were found interacting with most of the residues that establish contacts with CA on the PrTX-I/CA structure [18,35]. However, it is possible to determine, by checking electron density omit-maps, an unambiguous interpretation of CA for these maps (Fig 5). Moreover,CA molecules modeled on these maps presented lower mean B-factor values (55.7 Å2) when compared with sulfate ions modeled on the same region (88.9 Å2). For comparison reason, sulfate ions modeled in the same regionfor other Lys49-PLA2s structures presented following B-factor values: 44.2 Å2inPrTX-I/αT (PDB ID 3CYL); 68.8 Å2 in BthTX-I/αT (PDB ID 3CXI); and 52.9 Å2 in MTX-II/PEG4K (PDB ID 4K06).
The distances (Å) between protein inhibitorsare shownas yellow dashes for bump distances and red dashes for hydrogen bond distances. Residues of monomers A and B in contact with AAand CAare represented by sticks. Omit electron density maps for AA and CA molecules (gray meshes) were calculated with the coefficients 2|Fobs|-|Fcalc| contoured at 1.0 standard deviation.
In addition,three PEG 4000 moleculeswere noted in the PrTX-I/CA structure,with two PEGs inside the hydrophobic channels from both monomersand the third PEG moleculeinteracting with Lys7 on monomer B. The PEG molecules found in these sites are found in other Lys49-PLA2s structures [12,18,46]. Finally, in the PrTX-I/CA structure, a sulfate molecule establishedhydrogen bonds with Arg33 in monomer A, similarly to sulfate ions found in other Lys49-PLA2s structures [18,35].
On the other hand, in the PrTX-I/AA structure just one AA molecule was observedwhich established hydrogen bonds with N-terminalresidues from monomer B (Gly15 and Asn17 by two water molecules)in close proximity to the C-terminal region from monomer A, especially Leu121 (Fig 5). Moreover, AA established hydrophobic contacts withLeu121 and Pro123 from monomer A and with Lys7, Gln11 and Leu10 from monomer B (Fig 6). Furthermore, fivesulfate ionsinteracted with several basic residues ofthe PrTX-I/AA structure (Lys20, Arg34, Lys115 and Arg118), similarly to that observed in other Lys49-PLA2s structures. Finally, a part of a PEG 4000 molecule (nine atoms in the electron density map) inside the monomer B hydrophobic channelwas noted.
Structural comparison between apo-PrTX-I and complexes with PrTX-I crystal structures
Superposition among the complexed structuresPrTX-I/AA,PrTX-I/CA and PrTX-I rosmarinic acid (PrTX-I/RA) resulted in a Cα atom r.m.s. deviation in the range of 0.3–0.4 Å. In contrast, a similar superposition between thecomplexed structures and the apo structure had anr.m.s.d. close to 1.0 Å (Table 2). These values are comparable to other Lys49-PLA2s [35,48], where a pattern was observed among apo forms with an r.m.s.d. of approximately 1.0 Å, while for structures that present with molecules in the hydrophobic channel (e.g., PEG and α-tocopherol)these values are significantly lower. These higher values for apo forms occur mainly due to differences in their C-termini, demonstrating the higher conformational flexibility of this region. The main differences occur in three regions of each monomer: Ca2+ binding loop (residues 29–34), the loop after the β-wing (residues 85–90) and in the C-termini (117–130)(Fig 4). These differences are observed on several Lys49-PLA2s superpositions[12,18]and thus, the ligands do not cause relevant changes in the tertiary structure conformation of the protein.
Regarding the quaternary structure, PrTX-Istructures complexed to AA CA or RA have two protomers in the asymmetric unit (Fig 4) and present similar oligomeric structures. As observed for other bothropic Lys49-PLA2s , there are two choices of dimeric structure in their unit cells. However, there are several examples of experimental and functional data for this class of proteins showing that the oligomeric conformation known as the “alternative dimer” is the most likely to occur in solution(for a review refer to). Then, both PrTX-I structures were refined on this oligomeric conformation. In structures that present molecules in a hydrophobic channel solved in an alternative dimer conformation, it was observed that a Tyr119:Tyr119 interchain hydrogen bond is formed between the monomers. This interactionwas also observed for the complexedPrTX-I structures (AA, CA or RA) because these structures present PEG molecules in their hydrophobic channels. According to Fernandesand colleagues , PLA2-like structures with molecules at the hydrophobic channel are in their active state because the entrance of a molecule in this channel leads to a quaternary conformational change. This conformational change constitutes the first step of mechanism of action of these proteins. In addition, this phenomenon can be measured by the “two-angle model” previously proposed, which reflects the aperture and torsion of the dimer after molecular binding on hydrophobic channel . PrTX-I/AA,PrTX-I/CA and PrTX-I/RA have 40°,39° and 43° torsion angles and 27°, 28° and 23°aperture angles, respectively. These values are in agreement with structures in the active state [35,48]. In contrast, inactive (or apo) structures have higher values of torsion angles (60°-61°) and smaller values of aperture angles (6°-7°) [35,48].
The plant-derived molecules caffeic and aristolochic acids inhibit PrTX-I myotoxic activity
Several groups of indigenous people use specific plant extracts against snakebites, and the identification of their active compounds is an active field of study. Recently, some studies showed that several constituents of these plant extracts containanti-snake venom properties [19,21–23]. Recently, structural and functional studies demonstrated that rosmarinic acid (RA) was able to inhibit the invitro paralyzing activity caused by PrTX-I in mice neuromuscular preparationsby 80% . In addition, light and electron micrographs of mouse diaphragm muscle also demonstrated that PrTX-I may severely damage muscle fibers [47,49]. On the other hand, preparations exposed to PrTX-I that were pre-incubated with RA presented fibers with normal aspects .
In this study, both caffeic (CA) and aristolochic acids (AA) partially neutralized the muscle damage promoted by PrTX-I. As CA is a RA precursor, it was expected that its inhibitory activities against PrTX-I effects would be similar in the phrenic-diaphragm preparation. However, CA was ineffective at inhibiting the invitro paralyzing activity of this toxin. On the other hand, light microscopy analysis of muscle preparations submitted to myographic experiments showed that CA protected against the myotoxic effect induced by PrTX-I by 40% and 65% (PrTX-I/CA at ratios of 1:1 and 1:5, respectively). The different results between the CA and RA treatments probably was due to distinct interaction sites of these ligands with PrTX-I (see next two sectionsfor more detailed discussion about ligands binding). Similarly to CA, AA did not inhibit the neuromuscular blockade induced by PrTX-I. At a higher concentration (68.5 μg/mL), AA alone promoted negative effects on the phrenic-diaphragm preparation, where it caused twitches facilitated by an unknown mechanism. In addition, there were injured fibers in these preparations, which may explain the high muscle damage index when the PrTX-I/AA ratio was 1:5. Interestingly, at low concentrations (13.7 μg/mL), there was no such damage and AA promoted a partial protection (43%) to myotoxicity induced by the toxin (morphological analysis). Except for the intrinsic toxic effect of AA on the neuromuscular preparation, the toxin neutralization by AA and CA was similar, even though they interact in different regions of PrTX-I.
The paralyzing and muscle damage activities promoted by myotoxicLys49-PLA2s, represented here by PrTX-I, were due to their ability to alter the integrity of muscle cell membranes (for a review see ). After the initial binding, these myotoxins interact with sarcolemma and promote its destabilization, altering the permeability to ions (Na+, K+, Cl- and Ca2+) and macromolecules [8,50–53]. The first consequence of the ionic collapse is the cell depolarization and the lack of excitability due to the inactivation of voltage-dependent Na+-channels, thus impairing the generation of the action potential along the muscle fibers and determining the muscle paralysis. The continuous depolarization surrounding the endplate also reaches the motor nerve terminal, reducing the magnitude of the nerve action potential and consequently the acetylcholine (ACh) release, contributing to muscle paralysis [50, 54, 55]. Another consequence of the cell depolarization is the release of Ca2+ from intracellular pools , starting several deleterious effects, such as myofilament hypercontraction, mitochondrial damage and activation of Ca2+-dependent proteases and phospholipases [8,51,52], which culminates in the muscle injury [53,57].
Although the paralysis and the muscle fiber damage induced by Lys49-PLA2s are triggered by alterations in membrane permeability, the contractile process is more sensitive to such action because of its dependence on the cell excitability. Thus, ligands that partially inhibit the Lys49-PLA2 actions on cell membrane, such as CA and AA, promotes a partial protection of myotoxicity (up to 65% and 43%, respectively) with no positive interference on muscle paralysis. Corroborating this hypothesis, we have previously demonstrated that ligands able to promote a more effective binding to Lys49-PLA2, as rosmarinic acid, efficiently prevent both effects.
Aristolochic and caffeic acids bind to different regions of PrTX-I and cause myotoxic inhibition by two different mechanisms
Recently, Fernandesand coworkers proposed anactionmechanism for Lys49-PLA2s composed of five steps, which includes an allosteric transition and two independent sites of interaction with the target membrane: i)a cationic membrane docking site (MDoS), composed of the basic residues (usually Lys20, Lys115 and Arg118)responsible for the anchorage of the protein on membraneandii)a hydrophobic membrane disruption site (MDiS) composed of hydrophobic residues exposed to solvent (Leu121 and Phe125)responsible for the disruption of the membrane.
Interestingly, inthis study, we demonstrated that both ligands (AA and CA) are boundto residues related to MDoS and MDiS regions of the toxin and this fact may explain theirinhibitory characteristics. In the PrTX-I/CA crystal structure, four CA molecules interact with the protein. Two of them interact with Lys20, Lys115 and Arg118 residues for both monomers by hydrogen bonds and hydrophobic interactions (Figs 5 and 6). In other Lys49-PLA2 crystal structures, it is common to observe sulfate ions, whicharise from the crystallization conditions, establishing similar contacts with these residues[18,35]. Based on analysis of sulfate positions in PLA2 crystallographic structures,Bahnsonet alhypothesized that sulfate ions may simulatethe anion head of the phospholipid, revealing putative regions of the protein that could interact with the target membrane. This observation leddos Santos and colleagues to propose a similar hypothesis for Lys49-PLA2s, which was corroboratedbyFernandesand colleagues, who calledthis region the MDoS. Therefore, these data indicate that CA molecules inhibit PrTX-I myotoxic activity due totheir interaction withthe MDoS region and consequentlyavoid the docking of the toxinwith the membrane. Regarding the other CA molecules, an interaction with Gly15, Asn17, Ser21 and Leu121 residues close to the MDiS region was observed, suggesting that this CA molecule may also bind to the membrane disruption site of PrTX-I. The fourth CA molecule interacts with Lys100 and Glu108 residues butno function has beenassignedto these residues; thus,the binding of this molecule can be attributed to a non-specific interaction.
The crystal structure of PrTX-I/AAreveals an aristolochic acid molecule interacting by hydrogen bonds with Gly15(B) and via water molecules with Asn17(B) and Gln11(B) (Fig 5). This ligandalso interacts with the N-terminal portion of monomer B (Lys7, Leu10 and Gln11)andthe C-terminusof monomer A (Pro123),which isnearthe MDiS region (particularly Leu121). Therefore, based on this structural information, wepropose that the inhibitory feature observed for this ligand is due to the physical obstruction of the MDiSregion that impairs the disruption of the target membrane by the toxin.
The crystal structure of a catalytic PLA2(an Asp49-PLA2)from Viperarussellivenom complexed to aristolochic acid was also solved. Interestingly, this ligand binds in a different region compared to PrTX-I and the catalytic inhibition observed for this protein has adifferent structural basis. In the case of the structure fromV.russelli, the ligand is located at thehydrophobic channel of the protein, establishing hydrogen bonds with His48 and Asp49 and closing the entrance of its hydrophobic channel . The explanation for these binding differences between catalytic and non-catalytic PLA2s is probably thespecific amino acid differences between them because these proteins present a high level of secondary and tertiary structural conservation.
In conclusion, the data presented here demonstrate for the first timethe occurrence of two independent sites of interaction between a protein and a membrane target, whichcontributes to the validation of the proposed myotoxic mechanism [17,18].
How can we effectively inhibit bothropic Lys49-PLA2s?
One of the main challenges intoxicologytodayis to develop therapeutic alternatives to the treatment of snake venom injuries that are not efficiently neutralized by conventional serum therapy. In the case of Latin American snakes, the local myonecrosis caused by PLA2 and PLA2-like proteins is the main consequence of their envenomation. This effect is poorly neutralized by anti-venom administrationand, in many cases, may lead to injury, including amputation and permanent disability [5,6]. Therefore, it is important to understand the structural basis of local myonecrosis and to create molecular models than can guide the design of efficient inhibitors that could be used to complement conventional serum therapy. Furthermore, these models also could be used to develop new inhibitors for human PLA2s, which are involved in several inflammatory processes and present a very conserved tertiary structure in comparison to snake venom PLA2s.
In this work, we performed structural and functional approaches to provide substantial information about the inhibition of myotoxic Lys49-PLA2s using aristolochic and caffeic acids as molecular models. Taking into account the data presented here and previous studies reported in the literature with other ligands, we propose three different means to inhibit the myotoxicity caused by these proteins:
- physical blocking forphospholipid binding at the hydrophobic channel of the toxin. There are two different ways to achieve this blocking: a)by binding to the putative "active site" region (His48 residue) (e.g., pBPB) ,b) by preventing its occupation (e.g., rosmarinic acid) ;
- obstruction of the protein-membrane docking region (MDoS) (e.g., caffeic acid);
- obstruction of the protein region related to membrane destabilization (MDiS) (e.g., aristolochic acid).
AA and CA ligands provided relevant structural information about Lys49-PLA2s inhibition towards partial neutralization of the myotoxic activity of these proteins. These ligands experimentally highlighted the previously proposed mechanism of action of Lys49-PLA2s, binding with the two interaction sites of these proteins with the targetmembrane (MDoS and MDiS) . However, it is important to note that AA and CA ligands do not inhibitneuromuscular blocking activity. In contrast, RA efficiently inhibits the neuromuscular blocking activity (~90%) and neutralizes approximately ~80% of the myotoxic activity of PrTX-I . The analysis of crystal structure from PrTX-I/RA shows that RA causes the physical blocking of lysophospholipid-binding at the hydrophobic channel, in contrast to PrTX-I/AA and PrTX-I/CA structures, where the hydrophobic channel is completely empty (Fig 7). Cαsuperimposition betweenPrTX-I/AA, PrTX-I/CA and PrTX-I/RA structures shows that, in fact, AA, CA and RA bind in different regions of the protein (Fig 7). Furthermore, this superimposition also shows that RA causes the blocking of hydrophobic channel because a catechol group of RA occupies the same regionof part of the PEG molecule in hydrophobic channel present in PrTX-I/AA and PrTX-I/CA structures (Fig 7). Therefore, we can hypothesize thatan inhibitorsuch asRA, which is able toprevent the allosteric transition, aids more efficiently than a ligand (such as AA and CA) that blockades the MDoS and MDiS regions. These datasupport the observation that the binding of AA or CA only can occur efficiently after the allosteric transition, when the MDoS and MDiS regions are exposed to the solvent, with the protein in its active state and able to cause membrane lesion.
PrTX-I/AA and PrTX-I/CA were superimposed using their Cα atoms. The region that composes the hydrophobic channel are highlighted in yellow on molecular surfaces. (C)Structural comparison of binding mode of AA, CA, and RA on the PrTX-I structure. PrTX-I/AA, PrTX-I/CA and PrTX-I/RA weresuperimposed using their Cα atoms. AA, CA, RA and PEG are highlighted in blue, green, cyan and magenta sticks, respectively. The aminoacidsthat compose MDiS (Leu 121, in orange sticks), MDoS (Lys20, Lys115 and Arg118, in yellow sticks) and hydrophobic channel (Phe3, Lys7, Gln11 and Gly15, in green olivesticks) which interact with AA, CA and RA, respectively, are also highlighted.
The results presentedhere can promote the design of more accurate structure-based inhibitors that, to cause a full inhibition of Lys49-PLA2s activity could obstruct both the hydrophobic channel and the MDoS and MDiS regions. The putative drug formed by different inhibitors could obstruct all of these regions simultaneously. Finally, it is important to note that other PLA2s-like proteins (e.g., Arg49 and Ser49-PLA2s) also have a hydrophobic channel and analogous MDoS and MDiS regions . Consequently, the studies performed here may also be useful to study inhibition methods for these proteins and, consequently, provide an integrated inhibition mechanism for the entire PLA2-like protein class.
The coordinates were deposited in the Protein Data Bank (PDB) under the identification codes 4YZ7 (PrTX-I/AA) and 4YU7(PrTX-I/CA).
We also acknowledge the use of the Laboratório Nacional de Luz Síncrotron (LNLS, Brazil).
Conceived and designed the experiments: CAHF WGLC AMS MG MRMF. Performed the experiments: CAHF FFC WGLC AMS. Analyzed the data: CAHF FFC WGLC AMS MDP MG MRMF. Contributed reagents/materials/analysis tools: AMS MDP MG MRMF. Wrote the paper: CAHF FFC WGLC MG MRMF.
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