- Open Access
Inhibition by stabilization: targeting the Plasmodium falciparum aldolase–TRAP complex
- Sondra Maureen Nemetski†1, 9,
- Timothy J Cardozo†1, 2Email author,
- Gundula Bosch3, 8,
- Ryan Weltzer4, 8,
- Kevin O’Malley4, 8,
- Ijeoma Ejigiri5,
- Kota Arun Kumar6, 10,
- Carlos A Buscaglia7,
- Victor Nussenzweig6,
- Photini Sinnis3, 5, 8,
- Jelena Levitskaya3, 8 and
- Jürgen Bosch4, 8Email authorView ORCID ID profile
© Nemetski et al. 2015
Received: 11 June 2015
Accepted: 2 August 2015
Published: 20 August 2015
Emerging resistance of the malaria parasite Plasmodium to current therapies underscores the critical importance of exploring novel strategies for disease eradication. Plasmodium species are obligate intracellular protozoan parasites. They rely on an unusual form of substrate-dependent motility for their migration on and across host-cell membranes and for host cell invasion. This peculiar motility mechanism is driven by the ‘glideosome’, an actin–myosin associated, macromolecular complex anchored to the inner membrane complex of the parasite. Myosin A, actin, aldolase, and thrombospondin-related anonymous protein (TRAP) constitute the molecular core of the glideosome in the sporozoite, the mosquito stage that brings the infection into mammals.
Virtual library screening of a large compound library against the PfAldolase–TRAP complex was used to identify candidate compounds that stabilize and prevent the disassembly of the glideosome. The mechanism of these compounds was confirmed by biochemical, biophysical and parasitological methods.
A novel inhibitory effect on the parasite was achieved by stabilizing a protein–protein interaction within the glideosome components. Compound 24 disrupts the gliding and invasive capabilities of Plasmodium parasites in in vitro parasite assays. A high-resolution, ternary X-ray crystal structure of PfAldolase–TRAP in complex with compound 24 confirms the mode of interaction and serves as a platform for future ligand optimization.
This proof-of-concept study presents a novel approach to anti-malarial drug discovery and design. By strengthening a protein–protein interaction within the parasite, an avenue towards inhibiting a previously “undruggable” target is revealed and the motility motor responsible for successful invasion of host cells is rendered inactive. This study provides new insights into the malaria parasite cell invasion machinery and convincingly demonstrates that liver cell invasion is dramatically reduced by 95 % in the presence of the small molecule stabilizer compound 24.
Despite recent advances in treatment and prevention, malarial disease continues to afflict hundreds of millions of people every year, with growing resistance to current therapies [1–5]. Innovative treatments targeting hitherto under-exploited aspects of plasmodial biology are needed.
Plasmodium, as with other protozoan parasites belonging to the phylum Apicomplexa, progress through their life cycle by invading host cells. Gliding and active host cell invasion are thus crucial for these organisms, and are facilitated through an actin/myosin motor complex located beneath the parasite’s plasma membrane [6–8]. Herewith, the bridging enzyme PfAldolase, which binds actin in addition to its role in glycolysis , plays a key role: it connects the actin/myosin motor to trans-membrane adhesins of the thrombospondin-related anonymous protein (TRAP) family, which are expressed in a life-cycle stage specific manner . Thus, during plasmodial liver, blood and transmission stages, PfAldolase binds the conserved C-termini of the plasmodial paralogs TRAP, MTRAP and CTRP, respectively [10–15] as well as other interaction partners such as the cytoplasmic tail of AMA-1 .
The study presented here aims to inhibit parasite motility and infectivity by targeting the aldolase–TRAP interaction within the glideosome. As an enzyme of the glycolytic pathway, however, aldolase is well conserved throughout all kingdoms (204/365 identical residues between human and Plasmodium aldolase, see Additional file 1). Inhibitor design targeting the PfAldolase molecule and its binding partners must therefore meet the challenge of avoiding cross-reactivity with human aldolase enzymes. This study employs a novel approach to rational drug design to meet this challenge.
While traditional, targeted inhibitor-design approaches are usually geared towards finding small molecules that prevent protein–protein interactions (PPI) critical to the pathogen , the hypothesis explored here is counter-intuitive: strengthening, instead of hindering, the PfAldolase–TRAP interaction is hypothesized to inhibit motility and invasion. The rationale for this counterintuitive approach is that the hybrid molecular surface formed partly by PfAldolase and partly by TRAP in the bound state of the complex is unique to the parasite and could allow Plasmodium-specific targeting with small molecules that would not cross-react with the human orthologues (Fig. 1b). More importantly, a fast dissociation of bound TRAP-tails (after protease cleavage) is critical for Plasmodium’s ability to recycle PfAldolase molecules during gliding motility and host cell invasion [17, 18]. Therefore, a small molecule designed to strengthen the PfAldolase–TRAP interaction should render this crucial dissociation process slow and inefficient, thus leading to an imbalance of this dynamic system and concomitant locomotion defects and likely reduced cell invasion. Equally importantly, the ternary complex of PfAldolase–TRAP and a stabilizing agent would be expected to interfere with glycolytic activity as the active site is occluded. It is unknown if the liver stage parasite relies on glycolytic activity for energy generation as does the blood stage form of the parasite . However, PfAldolase is constitutively expressed in blood and gametocytes stages, suggesting it may be expressed, and is likely required, during liver stages as well (PlasmoDB PF3D7_1444800). A similar approach to stabilizing a PPI is described by Mecozzi et al. where they identified small molecules by virtual screening that were capable of stabilizing the Vps35–Vps26 interaction .
This hypothesis was tested using biophysical and biochemical assays as well as in vitro culture experiments with Plasmodium falciparum and Plasmodium berghei parasites to demonstrate that small molecules identified by virtual library screening (VLS) show an effect on gliding motility and hepatocyte invasion. A primary screen, which was comprised of VLS, PfAldolase catalytic activity, and thermal stability in the presence of small molecules, identified several compounds active in two or more assays. These were then further validated in two parasite specific assays, one investigating the impact on gliding motility and the second testing if parasites treated with small molecules are hindered in invasion of liver cells. Finally, the ternary co-crystal structure of PfAldolase–TRAP with compound 24 stabilizing the interaction was determined. The ternary complex is observed in all four copies of the PfAldolase tetramer represented in the crystal structure.
Compound library and chemicals
The screening library of 315,102 chemicals was provided as a structure description file (SDF) from the Chembridge Corporation (San Diego, CA, USA), as previously described. Unless otherwise noted, all compounds used in the in vitro and in vivo assays were obtained in powdered form from the Chembridge Corporation, and initially dissolved in 100 % DMSO to obtain 100 mM stock solutions, which were stored at 4 °C or −20 °C. Whenever possible, working dilutions in the relevant buffers were made within 24 h of the experiments in which they were used.
All computational work, including receptor modelling, VLS, docking, and hit-list post-processing was completed using tools in the ICM software suite produced by Molsoft, LLC (Version 3.7, La Jolla, CA, USA) with default parameters. VLS was performed as previously described . The PocketFinder function of ICM was used to render solvent pockets suitable for small molecule ligand binding on the molecular surface of 3D structural protein models as previously described . The crystal structure of the PfAldolase TRAP complex present in PDB ID 2pc4 was used as the starting point for all of the modelling, VLS and docking described in this study.
Expression and purification of Plasmodium falciparum aldolase
Cloning, expression, and purification of P. falciparum aldolase in Escherichia coli was performed using either of two previously described methods . Prior to catalysis assays, the GST-tag was removed from the tagged protein using the Novagen Factor Xa Cleavage-Capture Kit according to manufacturer’s instructions (EMD Biosciences, San Diego, CA, USA).
Synthetic peptides derived from the cytoplasmic tails of P. falciparum and P. berghei TRAP were custom-synthesized by Genemed Synthesis, Inc (TX, USA). These included PfTRAP25 (ETLGEEDKDLDEPEQFRLPEENEWN), PfTRAP6 (EENEWN), PbTRAP25 (VMADDEKGIVEDEGFKLPEDNDWN), and PbTRAP6 (EDNDWN).
Thermal shift assay
The results reported here measured the effect of the VLS hits on a complex of recombinant P. falciparum aldolase and the PbTRAP6 peptide described above. The assays were conducted and analysed as per previously published protocols in triplicates [27, 28].
Aldolase catalysis assay
The protocol utilized here was based on that provided by Sigma-Aldrich® (St. Louis, MO, USA), and all of the reagents (listed below) other than drugs, TRAP and aldolase were obtained from that company as well. Briefly, aldolase was pre-incubated for 10 min, +/− TRAP peptide (PfTRAP25, described above), +/− compound or DMSO at room temperature. The other reagents (α-GDH/TPI, β-NADH, F16P in order) were then added, yielding a final reaction mixture containing 0.02 units/ml aldolase (1 unit = amount of aldolase required to convert 1 μM of F16P to DHAP and G3P per minute at pH 7.4 and 25 °C; for these studies, this usually amounted to ~50 nM aldolase, based on an estimated purification yield of 10 units/mg aldolase), 2 mM F16P, 0.13 mM β-NADH, 2 units/ml α-GDH/TPI (1 unit = amount of αGDH required to convert 1.0 μM of DHAP to α-glycerophosphate per min at pH 7.4 and 25 °C), 100 nM TRAP (or DMSO), and 5–100 μM compound (or DMSO) in catalysis buffer (0.2 M glycine titrated to pH 7.3 with Trizma Base). A buffer with low ionic strength was used to avoid interference with the electrostatic interactions between aldolase and TRAP. Reactions were carried out either in a final volume of 1 ml, in standard plastic cuvettes (assays with PfTRAP25), or in a 96-well format with 100 µl reaction volume (assays with PbTRAP6). NADH consumption was measured at 340 nm for 10 min at 25 °C, using a SpectraMax M2e Microplate Reader (Molecular Devices, Sunnyvale, CA, USA). As many of the compounds had measurable inherent absorbance at 340 nm, the baseline absorbance of each compound when dissolved in catalysis buffer at the tested concentration was measured and subtracted from the values obtained during the kinetic run. Suramin, a known aldolase inhibitor, was used as a positive control for aldolase inhibition .
To test if compound 24 had an inhibitory effect on human aldolase, rabbit muscle aldolase was used, which is 99.3 % sequence identical to human aldolase. The assay was performed as described previously, however in the absence of TRAP-peptide to identify if the compound inhibited catalytic activity by itself.
Data collection and refinement statistics for PDB entry 4TR9
SSRL 12-2, micro focus
Resolution range (Å)
P 21 21 21
Unit cell (Å, °)
69.89 139.56 142.10 90 90 90
Mean I/sigma (I)
Number of non-hydrogen atoms
Ramachandran favoured (%)
Ramachandran outliers (%)
Surface plasmon resonance assay
A CM5 chip was prepared and conjugated with Neutravidin, allowing the subsequent capturing of biotinylated peptides, as described in . All experiments were carried out at 25 °C using a running buffer consisting of 10 mM Hepes pH 7.5, 150 mM NaCl, 1 mM MgCl2, 0.2 % Tween 20, 1 % DMSO. Purified PfAldolase was passed over a reference flow cell as well as over a PfTRAP-, PvTRAP- and PfMTRAP-tail exposing surface. Binding of PfAldolase was measured in the presence of different concentrations ranging from 125 to 1,000 µM of compound 24. All measurements were performed in triplicates interspersed by blank injections. Data analysis was carried out with Scrubber (BioLogic Software) using double referencing method and correcting for DMSO absorption effects.
Hepatocyte viability assay
The VLS hits were screened for their affects on cultured HC-04 hepatocytes (ATCC, Manassas, VA, USA) as previously described [35–37]. To determine toxicity of compounds 1, 3, 24, 42 and 43 on human hepatocytes, human hepatocyte cell line HC-04 capable of supporting P. falciparum development in vitro  was exposed to 1 mM of each compound for 96 h followed by Annexin V-APC and Propidium Iodide staining done according to manufacturer’s instructions (Apoptosis Detection Kit, eBioscience Inc, San Diego, CA, USA). Samples were analysed using flow cytometry (FACS-Scan, BD Biosciences) and the percentage of Annexin V negative/Propidium Iodide negative viable cells was calculated using FlowJo analysis software (Tree Star Inc, Ashland, OR, USA).
Sporozoite motility assay
Compounds were tested for their effect on P. berghei sporozoite motility using established protocols [39, 40] For the assays described here, sporozoites were pre-incubated with each compound at 500 μM for 10 min at 28 °C and the sporozoites remained in the presence of the compound (or DMSO) during the 1 h-long assay at 37 °C. The quantity of motile parasites, and the numbers of their trails were then calculated to assess the compounds’ effects.
Sporozoite invasion assay
The sporozoite neutralization assay was carried out as previously described . Briefly, P. berghei sporozoites were pre-incubated with 500 μM of the drugs or DMSO, and then allowed to infect human HepG2 cells (ATCC Collection). The HepG2 cells were collected after 40 h, and the infectivity of the parasites was quantified by real-time PCR using primers specific for the P. berghei 18S rRNA .
Identification of ligand-accessible pockets through VLS
Target site modelling
The precise conformation of the target pocket may strongly influence the selection of compounds by the VLS algorithm, as the target site is not flexible during the docking procedure. Therefore, in addition to screening the co-crystal structure of P. falciparum aldolase bound to a hexapeptide derived from the C-terminus of P. berghei TRAP6 (PDB ID 2pc4, ‘2pc4 model’), additional screens were carried out against two additional models of the complex generated in silico: one in which the P. berghei TRAP sequence (EDNDWN) was modified to its P. falciparum counterpart (EENEWN, ‘falciparum model’), and one in which the final TRAP residue was modified to alanine (EENDWA), in order to simulate induced fit via the ‘gapped-pocket’ method (‘gapped-pocket model’) . The different VLS receptor models and the areas in which the docking was concentrated are shown in Additional files 2 and 3.
Virtual hit group selection through target site docking
315,102 small molecules, representing a sub-set of the ChemBridge® hit2lead database (San Diego, CA, USA), were docked to the three different conformations of the target site using the ICM-VLS algorithm (Molsoft LLC, La Jolla, CA, USA). Three independent virtual screens against each receptor model, specifically targeting the PfAldolase–TRAP interface and surrounding residues, yielded 182 unique hits. To further narrow this preselection, these 182 compounds were re-docked to their respective receptors using the slower, more energetically accurate ICM-DOCK algorithm (Molsoft LLC, La Jolla, CA, USA). This step eliminated hits whose re-docked poses and/or energy scores differed significantly from the initial VLS results, as well as those with predicted lipophilicity (partition coefficients; cLogP) <−2 or >4. 60 of the 69 remaining compounds were then purchased from ChemBridge (San Diego, CA, USA) for in vitro and cell-based assay testing. The individual small molecule structures as well as details of the VLS and docking results for these 60 compounds are listed in Additional file 4.
In vitro hit validation by enzymatic activity and thermal stability assays
In keeping with the novel hypothesis presented here, the initial 60 docking hits were subjected to biochemical and biophysical tests to identify those small molecules that would actually enhance the PfAldolase–TRAP interaction and thereby occlude access of fructose 1,6-bisphosphate as a substrate to the active site of the enzyme (Fig. 1b). As mentioned above, TRAP binding has an inhibitory effect on aldolase’s glycolytic activity as previously demonstrated  (Fig. 1b).
Furthermore, the thermal stability  of the PfAldolase–TRAP complex was investigated with or without enzyme inhibition promoting hit compounds, in order to exclude effects resulting merely from structural destabilization due to compound addition. The melting temperature (TM) of the PfAldolase–TRAP complex was assayed in the presence versus absence of hit compounds, where a strongly negative TM-shift would indicate a destabilizing, denaturing effect. However, compounds causing only marginally negative TM’s or positive TM’s shifts compared to the PfAldolase–TRAP control were considered as potentially viable hits for further analysis (Fig. 3b, c).
At 100 μM final concentration of the compounds, 13 (compounds 3, 5, 14, 15, 18, 25, 26, 28, 33, 42, 43, 47, and 48) produced a positive shift of >2 °C in the melting point of a complex of recombinant P. falciparum aldolase and the same P. berghei TRAP hexapeptide used to solve the TRAP–aldolase co-crystal structure, suggesting a stabilizing effect (Fig. 3b, c). Interestingly, five compounds produced a negative TM shift of >2 °C compared to the control (compounds 3, 5, 14, 15, 43) when no TRAP-peptide was present, some of which could then be stabilized when TRAP was added (Fig. 3c, third panel).
Preliminary ligand based SAR analysis after primary screen
In vitro parasite hit validation by gliding motility and liver cell invasion assays
These same compounds, as well as compound 18, impaired the ability of parasites to invade hepatocytes when tested at 500 μM in a sporozoite neutralization assay [41, 42]. As shown in Fig. 5 and Additional file 6, compounds 18, 24 and 42 produced 58, 95 and 34 % inhibition of hepatocyte invasion, respectively as assayed by RT-PCR of P. berghei 18S ribosomal copy number. Interestingly, eight of the compounds (1, 3, 5, 19, 21, 29, 32, and 36) produced a trend towards increased infectivity of sporozoites.
Initial cytotoxicity study on human hepatocytes via flow cytometry
Ternary co-crystal structure confirms mode of action of compound 24
When comparing the predicted binding pose of compound 24 from VLS with the actual experimentally observed in the crystal structure, one can observe a reasonable good agreement of the proximity of the ligand (Additional file 12). The motion of the TRAP-peptide deeper into the PfAldolase active site introduces significant changes that currently cannot be computationally predicted a priori. When re-docking compound 24 to the actual observed ternary co-crystal structure (4TR9), the predicted pose results in a better overlap, with a preference for the binding mode 2 where the dichlorobenzyl-ring system is in contact with T44, K47 and R48 (Additional file 12).
Compound 24 does not cross-react with rabbit aldolase
Surface plasmon resonance (SPR) studies indicate decreased dissociation rates of the PfAldolase–TRAP complex in the presence of compound 24
Of note, recent studies have called into question the conservation of the gliding machinery across Apicomplexa, and in particular the role played by aldolase in infectivity. Shen et al. showed that one aldolase isozyme (TgALD1) can be knocked out, and the altered parasites retain infectivity, although to a much lower degree . In contrast, a recent study utilizing biolayer interferometry, as well as co-sedimentation studies, confirmed that aldolase and actin are required for Plasmodium for cell invasion of host cells , although this individual study is not considered definitive. The reader is referred to a recent comprehensive review discussing the similarities and differences of the glideosomes in Toxoplasma and Plasmodium  In addition to representing potential new leads in anti-malarial drug design, the compounds and methods described here represent an important new strategy for the field by providing new pharmacology (non-genetic) tools that may help clarify the Toxoplasma genetic studies. The most selective compounds could be valuable non-genetic tools for further investigating glideosome function in Plasmodium. At the concentrations tested, compound 24 did not inhibit rabbit aldolase, which was utilized as a surrogate for human aldolase with 99.3 % sequence identity (Fig. 9; Additional file 1). In addition, our studies suggest that the genetic findings in Toxoplasma may not apply to other biomedically important members of the Apicomplexan phylum .
Although proof-of-principle was achieved, the compounds exhibit relatively low potencies in functional assays, which is a limitation for their development into drug leads. Nevertheless, the potency of the hits themselves may be less important than validation of the target drug-binding pocket by structure-based screening: the pharmacophore space that is now mapped out by the hits and their bioactivities, in conjunction with the known interactions within the X-ray crystal structure, can serve as a blueprint for rational optimization of the hits in multiple directions (better potency, better bioavailability, etc.), using resources such as medicinal chemistry and fragment-based tethering. Notably, the GSK TCAMS  Novartis-GNF Malaria Box, and St Jude Children’s Research Hospital  datasets of hits from whole-cell screenings against P. falciparum blood stages include several compounds containing the N-(benzylideneamino)benzamide scaffold between them (Additional file 13). This scaffold is shared by some of the hits identified here (Fig. 4a), and medicinal chemistry derivatization of this scaffold may yield additional compounds with greater potency against the parasite or other favourable drug properties. It should also be noted that the average concentration of FDA approved drugs used to treat malarial disease in humans is close to 500 µM. For example, when injected intravenously the usual formulation of Chloroquine employed is 200 mg/ml, resulting in approximately 100 µM final concentration in the blood. Malarone, a combination therapy of atovaquone and proguanil is given as an oral dose at 750 mg/5 ml (~410 mM), corresponding to approximately 30 µM final concentration for a 60-kg person, assuming equal biodistribution throughout the body .
One intuitive, theoretical concern related to this study is that compounds targeted to the PfAldolase–TRAP interface may actually destabilize the complex or that stabilizing the target interface might enhance motility and infectivity. Indeed, several compounds showed destabilization on thermal shift. Notably, only the last three residues of TRAP (604–605) were visible in the crystal structure and receptor models which were screened against here. It is possible that these compounds interact in an inhibitory way with upstream TRAP residues that could not be accounted for in this screen. If so, these compounds may be the basis for a new approach to inhibit the glideosome as they should be even more specific. Destabilizing compounds, although not desired by the present design, may actually be useful from a drug development point of view once their exact mechanism of action is known. Additionally, eight compounds showed insignificant trends towards increases in invasion despite no change or decreases in motility, possibly indicating that some of the compounds may have additional off-target effects or change the PfAldolase–TRAP interaction in a way that increases invasion but not motility. As the precise chemistry and mechanism of the glideosome is still obscure, these possibilities cannot be ruled out. Compounds having this effect may nevertheless be useful non-genetic tools for studying precise glideosome sub-mechanisms.
Most drugs in use today inhibit biological interactions. However, the scientific literature contains several examples of biologically active small molecules that function by stabilizing protein–protein interactions in a bipartite manner, including fungal toxins [52–54], chemotherapeutic agents [55–59], antibiotics [60, 61], and immunosuppressants . These examples indicate, and the results here ultimately suggest, that it could be possible to develop clinically useful compounds that enhance PPI. For a small molecule to inhibit a PPI, it must bind to its receptor with a higher affinity than, and at least similar specificity to, the protein’s native ligand. A vast collection of failed drug candidates demonstrates how difficult it is to compete with eons of evolutionary pressure that produced the biomolecular interaction in the first place . Stabilizing that interaction, however, does not require competing with nature, as a nearby region is targeted by the small molecule. Rather, this approach tries to nudge the interaction’s equilibrium in the direction that is thermodynamically favoured to begin with. Thus a candidate enhancer does not need to bind either member of a protein complex with particularly high affinity—it is the aggregate of affinities of the proteins for each other and for the drug that matter . As demonstrated by the compounds discovered here, adding just one or two contact points to a protein complex can make a very big difference in its stability.
The enhancer approach may work especially well for situations in which the conformational dynamics of a protein complex are key to its function. In this case, the ability of the glideosome to provide the motive force is dependent on the highly coordinated interactions of its members. Aldolase must tightly bind both actin and TRAP to allow motion to begin, but it must also rapidly release the TRAP tail after its cleavage to allow motion to continue. While it is unclear if the same pool of aldolase participates in both motility and glycolysis, the enzymatic binding and cleavage of F16P is crucial for providing the ATP molecules necessary for the actin-myosin power stroke [29, 64]. The various conformations of aldolase, TRAP, actin, and MyosinA must therefore exist in the ideal equilibriums to promote the proper bind-and-release sequences for each of the glideosome interactions. Shifting these equilibrium in either direction by inhibiting or enhancing any of the interactions involved should affect the motor. The computer-aided, structure-based approach to drug discovery presented here allowed the specific targeting of structural differences between multiple conformations of aldolase in order to shift the apo-aldolase/aldolase-F16P/aldolase–TRAP equilibrium towards the aldolase–TRAP complex in a parasite-selective fashion. Nature abounds with similar vulnerable systems of exquisitely regulated biological motors and complexes, many of which might be targeted by this structure-based enhancer method.
Future modelling and crystallographic studies should help define additional receptor pockets and conformations that can be exploited to design compounds that target different aspects of the glideosome, including the glideosome homologs present in different stages of the Plasmodium life-cycle, as well as glideosome components conserved in other apicomplexan pathogens, such as Toxoplasma gondii and Cryptosporidium spp. For example, given sufficient structural information, the interactions between MTIP and Myosin A in Plasmodium could also be targeted in a similar fashion to the TRAP–aldolase complex by either stabilizing the close conformation or preventing opening of the EF-hands of MTIP. Several structures of PfMTIP and PkMTIP in complex with Myosin A [65–67] and stapled peptides [68, 69] have been described to date. Analysis of their structural flexibility may provide crucial insights towards targetable interfaces and pockets.
While stabilizing the PfAldolase–TRAP interaction may seem like an unusual approach for rational drug design, by targeting this joint surface, the avenue it opens to promoting parasite specificity—TRAP is not present in humans—may prevent the emergence of resistance. Additionally, resistance mutations in aldolase’s active site would be highly unfavourable as they would likely interfere with glycolytic energy generation. Starnes et al.  demonstrated in Toxoplasma that mutations near the active site of aldolase are not tolerated by the parasite, which is in agreement with the decreased likelihood of resistance mutations emerging.
The strategy of targeting a hybrid surface composed of a conserved target and a non-conserved target for the purposes of combating resistance may be broadly applicable to structure-based drug design. This may be especially useful for developing agents to fight eukaryotic pathogens, as many of their essential proteins have highly conserved human homologues, and are otherwise difficult to specifically target. It may also be possible to use this type of approach to design therapeutics for rapidly mutating viruses by selectively modulating host-pathogen interactions, i.e. preventing the dissociation of a viral surface protein with its host receptor may increase the virus’s vulnerability to other drugs or to the host’s own immune system. In this case, the druggable surface encompassing the viral protein would provide specificity, while the unlikelihood of mutations in the host protein may protect against the development of drug resistance. Similarly, one can envision targeting a complex of a normal housekeeping protein and a mutant oncoprotein to selectively kill cancer cells.
It is important to note that the compounds and chemical scaffolds identified here are not found among the anti-malarials currently in clinical use. The fact, that the identified compound emerged directly from a VLS effort and has not undergone any chemical optimization, while showing an on-target effect by various biophysical and parasitological assays bodes well for its future development from a probe to a lead compound. This effort, therefore, represents a successful ‘scaffold hop’ in anti-malarial drug discovery. If ultimately successful, these drugs and their derivatives would constitute a novel class or classes of anti-malarial agents, as well as the first drugs to target the aldolase–TRAP interaction.
At present, a more potent, safe drug with an identical mechanism of action to compound 24 could be useful for malaria prophylaxis, but its activity against merozoites, the extracellular form of the erythrocytic stage parasites was negative, likely due to the additional C-terminal extension of the merozoite TRAP homologue MTRAP occluding binding of compound 24. Nevertheless, if the compounds identified here do not cross-react with merozoites, a similar screen to that described in this study, targeting MTRAP, the merozoite homologue of TRAP, could yield a similar, specific drug active in the blood stages. Based on the sequence identity of the terminal residues of TRAP with CTRP, the circumsporozoite TRAP-like protein (PlasmoDB code PF3D7_0315200) expressed during the mosquito stage, it is anticipated that compound 24 may function as a stabilizer of the PfAldolase–CTRP interface and be able to block mosquito midgut invasion of the parasite. Such a compound could perhaps be used as a spray to treat bednets or to treat hatching areas and prevent spread of mosquitoes carrying the parasite.
In summary, the results presented here validate the aldolase–TRAP interaction within the Plasmodium glideosome as a drug discovery target, by proving both that it can be pharmacologically targeted and that doing so does affect the parasite’s motility and invasion capabilities. It remains to be determined, if a similar approach can succeed in Toxoplasma and other Apicomplexa, but using the chemical probes discovered here may contribute to the understanding of the role of aldolase in Toxoplasma gliding motility.
This work also provides proof-of-concept that the structure-based, selective, enhancement of PPI is a viable, efficient and effective method of novel drug hit discovery, opening new avenues to drug discovery for challenging targets, such as the glideosome.
The enhancer approach was initially conceived by SMN and TC. All computational work was performed by SMN under the guidance of TC. Aldolase plasmids were generated by CB, GB and JB. Synthetic peptides were designed by SMN, GB, JB, TC, CB, and VN. Catalysis assays were performed by SMN under the guidance of TC, and by KO and RW under the guidance of JB. Thermal shift assays and X-ray crystallography were performed by GB, KO and RW under the guidance of JB. Sporozoite motility assays were performed by IE under the guidance of PS. Invasion assays were performed by KAK under the guidance of VN. Hepatocyte toxicity assays were performed by JL. Surface plasmon resonance assays were performed by JB. All authors contributed to the writing and editing of the manuscript, as well as to scientific discussions and experimental design. All authors read and approved the final manuscript.
We thank Keren Klein, Lily Wu, Sandra Knoll, Dafna Gershoony, and Meredith Barton for technical assistance with experimental protocols. Lily Wu is also acknowledged for her helpful comments on the manuscript. We particularly thank Pete Dunten, Irimpan Mathews and the staff at SSRL beamline 9-2 and beamline 12-2, as well as Peter Zwart and the staff at ALS beamline 5.0.1 for their help and assistance during synchrotron data collection.
Protein data base (PDB) accession code
Coordinates and structure factors have been deposited with the PDB under accession code 4TR9.
This work was funded by NIH Grants DP2 OD004631 to TC, F30HL094052 to SMN, 5R01AI056840 to PS and a minority supplement to this grant to IE and by funding from the NYU MSTP program to SMN and IE. This work was partially funded through The Bloomberg Family Foundation (GB, RW, PS, JB), and a pilot Grant from the Johns Hopkins Malaria Research Institute (JL, JB).
Compliance with ethical guidelines
Competing interests A patent application based on the presented results has been submitted by TC, JB and SMN.
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