Open Access

Structural and functional characterization of the divergent Entamoeba Src using Src inhibitor-1

  • Luilli López-Contreras1,
  • Verónica Ivonne Hernández-Ramírez2,
  • Mayra Herrera-Martínez2,
  • Sarita Montaño3,
  • Luis Alejandro Constantino-Jonapa2,
  • Bibiana Chávez-Munguía2 and
  • Patricia Talamás-Rohana2Email author
Parasites & Vectors201710:500

Received: 14 March 2017

Accepted: 9 October 2017

Published: 18 October 2017



The abundant number of kinases that Entamoeba histolytica possesses allows us to assume that the regulation of cellular functions by phosphorylation-dephosphorylation processes is very important. However, the kinases responsible for the phosphorylation in Entamoeba spp. vary in the structure of their domains and, therefore, could be responsible for the unusual biological characteristics of this parasite. In higher eukaryotes, Src kinases share conserved structural domains and are very important in the regulation of the actin cytoskeleton. In both Entamoeba histolytica and Entamoeba invadens, the major Src kinase homologue of higher eukaryotes lacks SH3 and SH2 domains, but does have KELCH domains; the latter are part of actin cross-linking proteins in higher eukaryotic cells.


The function of the EhSrc protein kinase of Entamoeba spp. was evaluated using Src inhibitor-1, microscopy assays, Src kinase activity and western blot. In addition, to define the potential inhibitory mechanism of Src-inhibitor-1 for the amoebic EhSrc protein kinase, molecular dynamic simulations using NAnoscale Molecular Dynamics (NAMD2) program and docking studies were performed with MOE software.


We demonstrate that Src inhibitor-1 is able to prevent the activity of EhSrc protein kinase, most likely by binding to the catalytic domain, which affects cell morphology via the disruption of actin cytoskeleton remodeling and the formation of phagocytic structures without an effect on cell adhesion. Furthermore, in E. invadens, Src inhibitor-1 inhibited the encystment process by blocking RhoA GTPase activity, a small GTPase protein of Rho family.


Even though the EhSrc molecule of Entamoeba is not a typical Src, because its divergent amino acid sequence, it is a critical factor in the biology of this parasite via the regulation of actin cytoskeleton remodeling via RhoA GTPase activation. Based on this, we conclude that EhSrc could become a target molecule for the future design of drugs that can prevent the transmission of the disease.


Actin cytoskeleton EhSrc Entamoeba spp.Src inhibitor-1


In humans, E. histolytica causes invasive amoebiasis, which is an important source of morbidity and mortality in developing countries [1, 2]. Entamoeba invadens is the most important protozoan pathogen of reptiles [3].

Entamoeba spp. are simple eukaryotes that lack classical defined mitochondria, rough endoplasmic reticulum or Golgi bodies. However, trophozoites have very elaborate signaling machinery, through which they “feel” and interact with the different environments they find as they progress during invasion. These signaling pathways help the parasite to respond adequately to favor invasion and, therefore, are generally considered to be an important part of the interaction that the parasite establishes with the host [4, 5].

One of the most studied species in the genus Entamoeba is E. histolytica. In this protozoan parasite, the family of kinases is very abundant and these are part of the signaling systems of the parasite. The abundant number of kinases that Entamoeba histolytica possesses allows us to assume that the regulation of cellular functions by phosphorylation-dephosphorylation is very important. However, the kinases responsible for the phosphorylation processes in Entamoeba vary in the structure of their domains and, therefore, could be responsible for the unusual biological characteristics of this parasite [5, 6].

An example of these proteins is a homologue of the Src tyrosine kinase. Src kinases from higher eukaryotes share a conserved domain structure that consists of the consecutive peptide binding domains SH3, SH2, tyrosine kinase (SH1) domains, and SH4 domain; the last one always myristoylated, thus allowing the enzyme to be associated with the cell membrane. In the main homologue of the Src kinase from E. histolytica, SH3 and SH2 domains are absent. However, this molecule possesses KELCH domains, which strongly suggest its involvement in cytoskeleton regulation [6, 7]. These characteristics of the EhSrc protein kinase indicate that this enzyme diverges significantly from the closest homologous present in higher eukaryotes. Nevertheless, through the use of Src inhibitor-1, previous work from our group demonstrated its importance in amoebic movement and phagocytosis, as well as its role in the parasite’s virulence [8].

Src inhibitor-1 (4-(4′-phenoxyanilino)-6,7-Dimethoxy-N-(4-phenoxyphenyl)-4-quinazolinamine) is a potent, selective and competitive dual site (both ATP and peptide binding) Src kinase inhibitor that has been used to define physiological roles for Src family members in mammalian cells [9].

In this work, we describe structural and functional characteristics of amoebic Src. We demonstrate that Src inhibitor-1 diminishes Src activation in E. histolytica, which affects actin cytoskeleton remodeling, especially stress fiber formation and phagocytosis via defects in the formation of the phagocytic invaginations, without an effect on amoebic adhesion. Moreover, during the encystment in vitro of the model parasite E. invadens, the blocking of Src activity by Src inhibitor-1 affected encystment through the inhibition of RhoA activation. Therefore, this peculiar molecule and the significance of EhSrc or EiSrc activity in the biology of the parasite raise questions regarding its regulation and the potential to use EhSrc protein as a drug-target to prevent Entamoeba transmission.


Phylogenetic analysis

Phylogenetic and alignment analyses were conducted in the ClustalW package [10] with the amino acid sequences of 10 Src proteins from different species (E. histolytica, E. invadens, C. elegans, Mus musculus and Homo sapiens) obtained from the NCBI GenBank ( The sequence alignment and Neighbor-Joining tree were then manually edited [11, 12].

3D structure generation

The 3D structure of the EhSrc protein was built using I-TASSER server [13, 14], which yielded a cluster of different models from which the most energetically stable was selected. The following crystal structures were used as templates: Homo sapiens tyrosine protein kinase ZAP-70 (GenBank: 2OZO), Homo sapiens proto-oncogene tyrosine-protein kinase ABL1 (GenBank: 2FO0), Homo sapiens Tyrosine-protein kinase SYK (GenBank: 4FL2), Homo sapiens Tyrosine-protein kinase SRC (GenBank: 1FMK), Homo sapiens fibroblast growth factor receptor 2 (kinase domain) (GenBank: 2PSQ), Mus musculus proto-oncogene tyrosine-protein kinase ABL1 and the SH3-SH2 kinase domain (GenBank: 1OPK). The error associated with creating models using sequences and ab initio was refined by 100 ns of MD simulations to avoid bad internal atomic contacts. The structural alignment of the kinase domain between EhSrc and 2SRC (Homo sapiens) was performed in the Visual Molecular Dynamics (VMD) program [15, 16]. The ligand ISRC was built with Gaussian 03 using AM1 base [17].

Molecular dynamics simulations

The molecular dynamics (MD) simulations were performed in the Hybrid Cluster Supercomputer “Xiuhcoatl” at CGSTIC-CINVESTAV (, using NAMD 2.8 [18], which employed the CHARMM27 [19] using periodic boundary conditions in the MD simulations; Particle Mesh Ewald was used to account for electrostatic interactions [20]. The hydrogen atoms were added using the software psfgen from the VMD program [21]. The system was subjected to energy of minimization for 1000 steps followed by equilibration for 1 ns; the simulations were subsequently continued without restraints. The long MD simulations were run for 100 ns using the canonical NTV ensemble [22].

Trajectory analysis

The Carma program [23] was used for structural analysis to obtain the root mean square deviation (RMSD), the root mean square fluctuation (RMSF) and the radius of gyration (Rg), as well as the snapshot (100 ns) used for docking purposes [24].

Docking analysis

The protein-ligand docking studies, molecular graphics and protein visualizations were performed using the Molecular Operating Environment (MOE) program [25]. The studies for protein-protein docking were performed using Cluspro server [21]. Molecular graphics work and protein visualizations were performed with VMD.

EhSrc antiserum production

For the generation of a monospecific polyclonal antibody against EhSrc, the methodology described [26] was generally followed. A peptide (KEEISEDDGYGETQEE) from the catalytic domain of EhSrc (GenBank: EAL46348.1) was designed. The immunograde peptide was purchased from GL BIOCHEM, Shanghai Ltd. and used for rabbit immunization. A female white New Zealand rabbit was immunized 4 times with 1 week intervals for each injection. In the first immunization, 1 mg peptide and 500 μl of Freund’s complete adjuvant (Sigma-Aldrich, San Luis, MO, USA) were mixed and injected subcutaneously. For the subsequent immunizations, 1 mg peptide was mixed with Freund’s incomplete adjuvant (Sigma-Aldrich, San Luis, MO, USA) and injected. Before each immunization, blood was drawn by venous puncture from the rabbit ear and allowed to clot for 2–3 h at room temperature before preparation of sera. Titration of the specific polyclonal antibody was performed using Western blot (data not shown).

Parasite cultures and in vitro encystation

Trophozoites of E. histolytica (HM1-IMSS) and E. invadens (IP-1) were cultivated in TYI-S-33 medium [27] supplemented with 10% (v/v) bovine serum (BS) and 3% (v/v) Diamond vitamin-tween 80 solution (JRH Biosciences, Inc. St Louis, MO, USA) for 48 h in glass screw cap tubes (16 × 125 mm) at 37 °C. Trophozoites were subsequently incubated on ice for 10 min, collected by centrifugation at 1100 rpm for 10 min, and washed three times in TYI-S-33 medium without serum. Required number of trophozoites were then treated separately with 1% DMSO or Src inhibitor-1 (30 μM) (Merck, Darmstadt, Germany) for 2 h at 37 °C and washed with TYI-S-33 medium without serum.

To induce encystment, E. invadens trophozoites harvested in the logarithmic phase of growth (5 × 105/ml) were transferred to low glucose encystation medium (TYI without glucose) diluted to 47% with 5% bovine serum as described previously [28]. Trophozoites with or without Src inhibitor-1 (30 μM) treatment were incubated at 26 °C and, after 96 h, cysts were pelleted by sedimentation. The pellet was then re-suspended in 1 ml of 0.2% w/v Triton X-100 for 5 min. Cell counts were performed using a hemocytometer, and the number of detergent-resistant cysts was determined. Cysts were fixed and stained with white Calcofluor m2r (Sigma-Aldrich, St. Louis MO, USA), a fluorescent dye with specific binding to chitin molecules.

Entamoeba histolytica Adhesion assays

As described earlier by López-Contreras et al. [8], after being treated with Src inhibitor-1 or DMSO for 2 h, trophozoites (2 × 105) were washed with TYI-S-33 without BS to eliminate drug residues, and then the cells were incubated in TYI-S-33 without BS for 10 min in 96-well black plates (BD Cellware, Bedford, MA, USA) at 37 °C. Non-adhered cells were eliminated, and adhered cells were stained with Sytox Green (1:5000) (Molecular Probes, Eugene, OR, USA), then adhered cells were washed with PBS and fluorescence was measured at 488 nm in a fluorometer (Fluoroskan Ascent FL, Thermo, Boston, MA, USA). Fluorescence from DMSO-treated trophozoites was defined as 100% of adhesion.

Immunoprecipitation and western blot assays

Immunoprecipitation assays were performed as previously described [29]. Briefly, trophozoite lysates (1 mg of total protein) were precleared with protein G-agarose (Gibco-BRL, Grand Island, NY, USA) (previously blocked with 2% bovine serum albumin) for 2 h at 4 °C. The anti-EhSrc serum (1/1000) was then added to the cell lysates supernatant. Mixtures were incubated overnight at 4 °C, and then 2% bovine serum albumin (BSA) blocked protein G-agarose was added and incubated for another 2 h at 4 °C. Agarose beads were recovered by centrifugation at 11,600× g for 2 min at 4 °C, washed with 10 mM Tris-HCl pH 7.4, containing 150 mM NaCl, 3 mM EDTA, and 1% Nonidet P-40, resuspended in Laemmli’s sample buffer, and boiled for 5 min. After centrifugation, supernatants were loaded onto a 10% SDS-polyacrylamide gel electrophoresis and then processed as described previously with anti-phosphotyrosine (1/1000), anti-actin (1/1000), anti-EhSrc (1:50,000) antibodies and their respective secondary antibodies.

Src kinase activity assays

After immunoprecipitation (1 mg of total protein) with EhSrc antibody (1:1000), immunoprecipitates were analyzed using a Pro-Fluor® Src-Family kinase assays (Promega, Fitchburg, WI, USA) according to manufacturer’s instructions. The fluorescence was read at a wavelength of 525 nm and Src kinase activity present in immunoprecipitates of DMSO-treated trophozoites was defined as 100%.

Confocal microscopy assays

Analyses by confocal microscopy were done as described previously [30], with slight modifications. Trophozoites incubated on coverslips, with or without Src inhibitor-1 treatment, were fixed with 4% formaldehyde, blocked with BSA for 1 h at 37 °C, and incubated overnight with an anti-phospho-Src antibody (1/50) (Cell Signaling Technology, Danvers, MA, USA) or anti-EhSrc (1/250). Cells were then washed with PBS and incubated with Fluorescein-isotiocyanate (FITC)-labeled goat anti-rabbit immunoglobulin G (IgG) (1/100) (Jackson ImmunoResearch, Pennsylvania, USA) secondary antibody. Actin was stained with rhodamine-phalloidin (1:25) (Molecular Probes, Oregon, USA) for 30 min at 37 °C. Coverslips, which were mounted with Vectashield (Vector Laboratories, Ontario, Canada), were analyzed by confocal microscopy in a Laser Scan Microscope 700 (Carl Zeiss, Oberkochen, Germany). The intensities of fluorescence were obtained with the software ZEN BLUE 2017 and the Pearson’s coefficient was calculated with the SPSS version 24.

Scanning and transmission electron microscopy assays

As described by González-Robles et al. [31], trophozoites with or without Src inhibitor-1 treatment were fixed with 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer, pH 7.2, dehydrated with increasing concentrations of ethanol, and critical point dried using a Samdri apparatus. Then, samples were gold coated in an ion-sputtering device (JOEL-JFC-1100, Jeol USA Inc., Peabody, MA, USA) and examined with a Zeiss DSM 982 Gemini scanning electron microscopy. For transmission electron microscopy, samples were fixed in 2.5% (v/v) sodium cacodylate buffer, pH 7.2, for 1 h, and then they were post-fixed for 1 h with osmium tetroxide in the same buffer. After dehydration in increasing concentrations of ethanol and propylene oxide, samples were embedded in polybed epoxy resins and polymerized at 60 °C for 24 h. Thin sections (i.e. 60 nm) were contrasted with uranyl acetate and lead citrate prior to examination in a Joel JEM-1011 transmission electron microscope.

Measurement of RhoA activity

RhoA activity was determined using a luminescence based G-LISA™ RhoA activation assay kit (Kit #BK121, Cytoskeleton, Inc., Denver, CO, USA), according to the manufacturer’s instructions. This assay employs a GTP-binding protein that coats the wells of a 96-well plate. Active GTP-bound GTPases in cell lysates bind to the wells, whereas inactive GDP-bound GTPases are removed through washing steps. The bound active protein is subsequently detected by incubation with a specific antibody followed by a HRP-conjugated secondary antibody and a detection reagent, after which the luminescence is read on a microplate luminescence reader. A calibration curve with a positive control was performed, and the results are shown as ρg of protein-GTP/μg protein extract.

Statistical analysis

Data are representative of two independent experiments, each one done in triplicate. The significant differences of experimental compared with control samples were analyzed by Student’s t-test using the Statistical Package for the Social Sciences (SPSS), version 24.

Results and discussion

Homology modeling of the divergent EhSrc

A BLAST search of human Src (hSrc) (GenBank: NP_938033) in the genomes of E. histolytica and E. invadens led to the identification of several kinases. The alignment between E. histolytica Src (EhSrc; GenBank: EAL46348.1) and E. invadens Src (EiSrc; GenBank: XP_004258856.1) showed a 29.135% homology between them. In comparison, the alignment between hSrc and EhSrc, presented a 15.013% homology, whereas the alignment between hSrc and EiSrc, showed a 13.87% homology (Fig. 1a). When performing a phylogenetic analysis it was evident that EhSrc and EiSrc are highly divergent from their closest homologues in higher eukaryotes (Fig. 1b). It has been described that the Src protein of E. histolytica has a kinase domain (Fig. 1c), lacks SH2 or SH3 domains but has KELCH 1 and KELCH 4 domains [6], whereas the Src protein from E. invadens (GenBank: XP_004258856.1) also lacks SH domains but has a KELCH 6 domain (Fig. 1c). KELCH proteins and KELCH-like proteins are a group of proteins that contain multiple KELCH motifs that form β-propellers to undergo a variety of binding interactions with other proteins, notably the actin filaments of a cell [32].
Fig. 1

EhSrc is highly divergent from its closest homologues. a Alignment of the conserved domain among EhSrc (EAL46348.1), EiSrc (XP_004258856.1) and human Src (NP_938033). Identical amino acid residues are in dark gray and similar amino acid residues in light gray. b Phylogenetic tree of Src proteins of E. histolytica, E. invadens, Homo sapiens, Mus musculus and C. elegans. EhSrc protein of E. histolytica shows the highest homology with the Src protein of E. invadens, and these two proteins are poorly related with Src proteins from mammals as well as the nematode C. elegans. c Structural domains of typical Src and EhSrc proteins from E. histolytica and E. invadens are shown. The typical Src is composed of an amino-terminal myristoylation sequence (M), a unique region (U), Src-homology-2 (SH2) and SH3 protein-interaction domains; the Src of Entamoeba lacks these domains with the exception of the kinase domain

The 3D structure of EhSrc (GenBank: EAL46348.1) was performed using I-TASSER server [12]. It presented a normalized Z-score of 3.29 for 2OZO; 2.82 for 2FO0; 4.22 for 2SRC; 2.24 for 4FL2; 3.03 for 1FMK; 0.81 for 2PSQ; and 4.22 for 1OPK. Alignment was with a normalized Z-score > 1, meaning a good alignment. According to the 3D model obtained from the I-TASSER server, EhSrc protein is a globular protein that contains 750 amino acid residues (Fig. 2a). After 100 ns of MD simulations, the protein exhibits sixteen α-helices and thirteen β-sheets, whereas the rest of the structure is formed by coil structures. In addition, Tyr 586 (amino acid equivalent to Tyr 416 in a typical Src) within the catalytic site (constituted by the 430 to 730 amino acid domain) in the EhSrc protein, has the potential to be phosphorylated during activation.
Fig. 2

Homology structural modeling of EhSrc. a 3D model of EhSrc. b The structural alignment of EhSrc kinase domain in red and 2SRC kinase domain in cyan. c RMSD of EhSrc at 100 ns of trajectory on MD simulation. d Rg of EhSrc at 100 ns of trajectory on MD simulation. e RMSF of EhSrc at 100 ns of MD simulation

The kinase domain (from 430 to 730 amino acids) of the 3D model obtained with I-TASSER for EhSrc and the crystal structure of human tyrosine kinase (2SRC) from 269 to 519 amino acids were structurally aligned (Fig. 2b) and the value of RMSD (distances between residues) was 0.765. This result suggests that the kinase domain is conserved in the EhSrc protein kinase; this region in the human tyrosine kinase contains an Y416 which is a phosphorylation site, whereas in the EhSrc protein this Y residue is in the 586 position. This would explain why pSrc antibody against human Src recognized the phosphorylated form of EhSrc (Fig. 3b).
Fig. 3

Src inhibitor-1 inhibits EhSrc protein activation of E. histolytica in silico and in vivo. a Predicted binding site of Src inhibitor-1 in the EhSrc protein of E. histolytica. b Confocal microscopy analysis of trophozoites with or without Src inhibitor-1 (30 μM) treatment. Actin was stained with rhodamine-phalloidin (red) (1/25), the nucleus was identified with DAPI 1/300 (blue) and p-Src (green) was detected with an anti-p-Src antibody (1/50). c Detection by western blot of phosphorylated tyrosine (p-Tyr), actin (α-actin) and EhSrc in EhSrc immunoprecipitated complex from treated and non-treated trophozoites with anti-phospho-tyrosine (1/1000), anti-actin (1/5000), and anti-EhSrc (1/5000) antibodies. d The kinase activity of DMSO- and Src inhibitor-1-treated trophozoites was determined using a Pro-Fluor® Src-Family kinase assays (Promega, Fitchburg, WI, USA) according to manufacturer’s instructions; the kinase activity from DMSO-treated trophozoites was defined as 100%. Values for each group represent mean ± SEM results from three independent experiments

To predict the place where Src inhibitor-1 is binding to the EhSrc molecule in amoebic trophozoites, MD simulations using NAMD2 were performed and the docking studies were done using Moe software.

The MD simulations results of EhSrc were submitted to structural analyses, such as the RMSD, the Rg and the RMSF as described [33]. The RMSD trajectory analysis shows the convergence during the MD simulation and its normalization reveals whether the values pursue a normal distribution. Normalized RMSD of Src indicates that the protein reached the equilibrium after 80 ns of MD simulation (Fig. 2c). Other E. histolytica proteins have been modeled and MD simulated just up to 10 ns [34, 35], this MD simulation analyses up to 100 ns are enough to predict reliable models for these proteins.

The Rg is a geometrical parameter that defines the protein expansion and compactness; we thus evaluated the compactness of the system. The Rg increased in the first 0 to 25 ns, and from 30 to 60 ns the slope was constant; however, from 60 to 70 ns, it increased, and from 70 to 100 ns, it became almost constant (Fig. 2d).

Additionally, we located the protein flexible regions via measurement of the RMSF values of the Cα backbone (Fig. 2e). The principal peaks of the flexible regions were located the first one, in 50 to 100 amino acid residues, with a displacement from 5 to 15 Å. The second peak was located at 250 to 350 amino acid residues, where the displacement changed from 5 to 15 Å. The third region was identified at 400 to 520 amino acids with a displacement of 7 to 13 Å. The last peak, where Tyr 586 is located, was identified from 560 to 650 residues, and it presented a displacement of 7 to 15 Å (Fig. 2e). These last regions belong to the catalytic domain, which explains the motion of these residues.

Src inhibitor-1, an inhibitor of typical Src also reduces EhSrc activity

In silico analyses demonstrated that the kinase domain of Src is present in EhSrc and this sequence is a target for Src inhibitor-1. To analyze the possibility of binding between the EhSrc and Src inhibitor-1, docking studies were performed in MOE. This study demonstrated that Src inhibitor-1 binds to the amino acids Lys 548, Val 550, Lys 580, Glu 585, Tyr 586, Gly 608, Ile 609 and Phe 610 in the EhSrc (Fig. 3a). These findings indicate that Src inhibitor-1 interacts with Tyr 586 (the equivalent of Tyr 416 in a typical Src), which is responsible for the ATP binding necessary for Src activation and thereby inhibits its phosphorylation. These results suggest that Src inhibitor-1 could affect EhSrc activation in E. histolytica by binding to the catalytic domain in the site where ATP binds. To confirm this hypothesis, we used a polyclonal antibody that recognizes the phosphorylated form of Src.

Live trophozoites, with or without Src inhibitor-1 treatment, were analyzed by confocal microscopy for activated Src detection; Src inhibitor-1 reduced Src activation in live trophozoites. Furthermore, this inhibitor affected actin cytoskeleton remodeling, particularly fiber stress formation (Fig. 3b). Additionally, EhSrc from trophozoites, treated or not with Src inhibitor-1, was immunoprecitated with the polyclonal anti-EhSrc antibody and blotted with anti-phospho-tyrosine antibody. Results showed that Src-inhibitor reduced EhSrc phosphorylation in trophozoites, compared to DMSO-treated trophozoites (Fig. 3c). Furthermore, EhSrc activity was measured in the immunoprecipitate using Pro-Fluor® Src-Family kinase assays (Promega, Fitchburg, WI, USA) and results demonstrated a significant reduction (t-test: t (4) = -8.174, P = 0.001) in EhSrc activity in Src inhibitor-1-treated trophozoites in comparison with DMSO-treated trophozoites (Fig. 3d). These results demonstrate that EhSrc can be inhibited by Src inhibitor-1, most likely by binding to the catalytic domain as it occurs in other types of Src in higher eukaryotic cells.

Divergent EhSrc interacts with actin

EhSrc contains KELCH domains, which typically are involved in protein-protein interactions and are also largely involved in the regulatory functions of the cytoskeleton. To corroborate the EhSrc kinase participation in actin cytoskeleton regulation and its binding to actin, we analyzed fibronectin adhered trophozoites using confocal microscopy to identify the presence of EhSrc using an anti-EhSrc antibody during actin cytoskeleton remodeling. Results demonstrate that EhSrc kinase co-localizes with F-actin during actin cytoskeleton remodeling (Fig. 4), mainly in actin structures such as cortical actin (Fig. 4b) or phagocytic invaginations (Fig. 4c), where the Pearson coefficient R values were 0.589 and 0.93, respectively. In contrast, within a representative cytoplasm region, there was no correlation between both proteins (R = -0.11). The docking analysis suggests the possible binding between actin and EhSrc through involvement of different amino acids, including amino acids of KELCH 1 domain, V148 and I150, which interact with R40 of actin (Fig. 4d; Additional file 1: Figure S1). KELCH domains are conformed by a set of five to seven KELCH repeats that form a β-propeller tertiary structure [32]. However, in this analysis it was not possible to identify the β-propeller tertiary structure characteristic of KELCH proteins, within the KELCH 1 domain of EhSrc kinase, at least theoretically. However, here we found that this domain participates in its interaction with actin, and some of the residues of the EhSrc protein which are involved in the binding to actin belong to the kinase domain (Additional file 1: Figure S1). In Drosophila, KELCH protein is an actin filament cross-linking protein essential for the organization of actin via Src kinase [36, 37].
Fig. 4

EhSrc interacts with actin during actin cytoskeleton reorganization. a Confocal microscopy analysis of trophozoites adhered to FN; actin was stained with rhodamine-phalloidin (red) (1/25), and Src (green) was detected with EhSrc antibody (1/250) and FITC-labeled goat anti- rabbit IgG (1/100). The white arrows in the merged image indicate the colocalization sites. At the bottom of panel (b) and to the right of panel (c), histograms of green and red intensities corresponding to selected areas (white boxes in confocal images) are shown. Areas of colocalization are marked with yellow arrows; areas where no colocalization was found are marked with green arrows. In each panel (b and c), the dispersion values indicating the results of the colocalization analyzes​​ are shown. d Predicted binding site of EhSrc and actin of E. histolytica. Image processing was performed with the Zen Blue software (v. 2012); the Pearson correlation coefficient was calculated with the SPSS software (v. 24). Abbreviation: R, Pearson correlation coefficient. Scale-bars: 10 μm

Actin-EhSrc interaction was corroborated by co-immunoprecipitation of EhSrc and actin (Fig. 3c), which suggests that EhSrc protein could participate in the actin cytoskeleton regulation, even though it has an unusual amino acid sequence. However, the possible mechanism by which EhSrc regulates the actin cytoskeleton could be different from that reported in other higher eukaryotic cells, where KELCH proteins are phosphorylated by Src to regulate the actin-KELCH interaction [37].

Furthermore, Src inhibitor-1 provokes disruptions in the actin cytoskeleton remodeling during trophozoites adhesion (Fig. 3b), which we have previously reported [8], supporting our hypothesis that EhSrc kinase, in spite of having an unusual structure, is able to regulate the actin cytoskeleton remodeling.

EhSrc participates in the formation of structures involved in erythrophagocytosis, and in encystment, but not in amoebic adhesion

Typically, Src kinases act downstream of integrin receptors and are implicated in cell adhesion [7]; thus, we evaluated the role of Src inhibitor-1 in the cell adhesion of E. histolytica. The results demonstrate that inhibition of EhSrc activity did not affect adhesion of E. histolytica trophozoites (Additional file 2: Figure S2). When observed by scanning electron microscopy, trophozoites treated with DMSO exhibited a diverse morphology with wrinkled cell surfaces and numerous holes (crater-like depressions); these trophozoites also developed filopodia and lamellipodia in the basal area. However, Src inhibitor-1 causes remarkable ultrastructural changes in trophozoites: the cell surface becomes smoother, the holes or crater-like depressions are significantly reduced, the filopodia are absent and the lamellipodia are shorter. Despite these differences, trophozoites treated with Src inhibitor-1 remained adhered (Fig. 5a, upper panels). Using transmission electron microscopy, we identified defects in the formation of phagocytic invaginations in Src inhibitor-1 treated trophozoites compared with DMSO-treated ones (Fig. 5a, lower panels). As observed in these images, also the number of vesicles per cell in trophozoites treated with Src inhibitor-1 diminished (Fig. 5a lower right panel) when compared with DMSO-treated trophozoites. To confirm this observation, intracytoplasmic vesicles were counted in 71 DMSO-treated amoebas and 124 Src inhibitor-1-treated amoebas, in semi-thin sections stained with Toluidine blue. No statistical difference was observed between trophozoites treated with Src inhibitor-1 and those treated only with the vehicle (data not shown).
Fig. 5

EhSrc participates in the formation of structures involved in erythrophagocytosis but not in amoebic adhesion. a Upper panel: scanning electron microscopy; lower panel: transmission electron microscopy analyses of trophozoites of E. histolytica with or without Src inhibitor-1 treatment adhered to nylon grids. b Trophozoites of E. histolytica with or without Src inhibitor-1 treatment interacted with human erythrocytes for 5 min (upper panel) or 15 min (lower panel), analyzed by scanning electron microscopy

Src kinase activity is present in phagocytic cells, and Src-deficient cells are less effective compared with wild-type cells in the mediation of phagocytosis [38]. Previously, a remarkable reduction in phagocytic capacity of E. histolytica was reported when trophozoites were treated with Src inhibitor-1 [8]; however, the mechanism by which Src inhibitor-1 inhibits this important amoebic function remains unknown. Here, trophozoites incubated with human erythrocytes were analyzed by scanning electron microscopy. DMSO-treated trophozoites developed numerous phagocytic invaginations, whereas Src inhibitor-1-treated trophozoites did not exhibit these structures or they were incomplete (Fig. 5b). These results indicate that Src inhibitor-1 affects the formation of phagocytic structures most likely via disruption of the actin cytoskeleton remodeling (Additional file 3: Figure S3).

On the other hand, it has been demonstrated that chelerythrine chloride, staurosporine, and wortmannin inhibit the encystation of E. invades, which suggests an important role of kinases in this essential process of the parasite [39, 40]. We explored the potential role of EhSrc in the encystment of E. invadens (a model used to study encystation for the genus Entamoeba) through the use of Src inhibitor-1. Src inhibitor-1 inhibited cyst formation at 72 h post-induction of encystment, which significantly reduced the number of cysts, when compared with DMSO (Fig. 6a, b) (t-test: t (10) = 23.683, P < 0.001).
Fig. 6

Src inhibitor-1 blocks encystment process and GTP-RhoA activity. a Percentage of cyst formation inhibition by Src inhibitor-1 treatment (30 μM) during 96 h. Calcofluor m2r staining of cysts produced in each condition. b E. invadens trophozoites were induced to encyst in the presence of Src inhibitor-1 or vehicle (DMSO); after 12 h of encystment, the level of RhoA-GTP was determined with a G-LISA RhoA activation assay kit (Kit no. BK121, Cytoskeleton, Inc., Denver, CO, USA), according to the manufacturer’s instructions

It has been demonstrated that the actin cytoskeleton plays different roles during the encystment of E. invadens, such as morphological changes, transportation and disposal of vacuoles, and the transport of encystment vesicles from the cytosol to the cell wall. The actin cytoskeleton reorganization largely depends on RhoA-GTP; this result is consistent with a previous report in which the participation of RhoA-GTP was demonstrated to be important for the encystment process through actin cytoskeleton reorganization [41, 42].

The involvement of RhoA in the actin cytoskeleton organization during the early period of the encystment process of E. invadens has been demonstrated [41], which indicates that RhoA is essential for encystment. Therefore, we analyzed the role of EhSrc activity on RhoA activation during the encystment of E. invadens. The findings demonstrate that Src inhibitor-1 reduces RhoA activation (Fig. 6c) (t-test: t (6) = 4.984, P = 0.002), which indicates the potential mechanism by which EhSrc regulates the actin cytoskeleton reorganization. Cdc42 and Rac1 activities were also assayed, but no activation could be detected during E. invadens encystment (data not shown).


The large number of protein kinases in Entamoeba suggests that phosphorylation is an important regulatory mechanism of this intriguing and ancient parasite. Although Entamoeba has complex networks of cell signaling, it exhibits important differences compared with higher eukaryotic cells, which could be used for the design of anti-amoebic drugs to prevent transmission. While the EhSrc is highly divergent from its closest homologues in higher eukaryotes, it regulates important cellular functions, such as phagocytosis or the encystment process, through actin cytoskeleton regulation, which leads us to propose that amoebic kinases could be important targets to prevent amoebiasis infection.



Bovine serum


Bovine serum albumin


Dimethyl sulfoxide


Divergent Entamoeba histoyltica Src


Divergent Entamoeba invadens Src


Fluorescein IsoTioCyanate


Enzyme that binds and hydrolyzes guanosine triphosphate


Human Src


Immunoglobulin G


Molecular Operating Environment


NAnoscale Molecular Dynamics


Particle Mesh Ewald


Radius of gyration


Root mean square deviation


Root mean square fluctuation


Non-receptor tyrosine kinase


Visual Molecular Dynamics



The authors acknowledge the General Coordination of Information and Communications Technologies at CINVESTAV for providing HPC resources on Hybrid Cluster Supercomputer “Xiuhcoatl”. The authors acknowledge Héctor Manuel Oliver Hernández responsible of CGSTIC, Roberto Issac Cuevas-Hernández and Anel Lagunes-Guillén for their technical support. MVZ Octavio Ramos Flores from UPEAL-CINVESTAV for his help with the production of the rabbit polyclonal antibody.


This research was supported by CONACyT, Mexico (Grants No. 104108 and 221136-M-1370 to PTR). LCL was a recipient of a CONACyT fellowship (211715).

Availability of data and materials

All data generated or analyzed during this study are included in this published article and its additional files.

Authors’ contributions

LCL and TRP designed the study and wrote the manuscript. All authors performed the experiments: HRVI and CMB carried out microscopy analysis, CJLA designed the antigenic peptide and produced the anti-EhSrc antibody; also performed the confocal image analysis, HMM carried out encystment and GTPase analyses and MS carried out in silico analysis. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The research protocol was approved by CINVESTAV’s Institutional Animal Care and Use Committee (CINVESTAV-IACUC). The procedures were approved by the board of the Animal Production and Experimentation Unit (UPEAL, CINVESTAV). Antibody production was performed with a rabbit provided by UPEAL-CINVESTAV, (Protocol No. 0053–13) following the specifications of the Mexican National Norm (NOM-062-ZOO-1999) that is a version of the guide for the care and use of laboratory animals 2011.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

Área Académica de Medicina, Instituto de Ciencias de la Salud, Universidad Autónoma del Estado de Hidalgo
Departamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del I.P.N
Facultad de Ciencias Químico Biológicas de la Universidad Autónoma de Sinaloa, Calz. de las Américas Norte 2771


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