Original Research ARTICLE
In Silico Study of Alkaloids as α-Glucosidase Inhibitors: Hope for the Discovery of Effective Lead Compounds
- 1Department of Pharmacy, Abdul Wali Khan University, Mardan, Pakistan
- 2Department of Chemistry, University of Swabi, Swabi, Pakistan
- 3Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad, Pakistan
- 4Department of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan
α-Glucosidase (extinction coefficient 18.104.22.168) is a primary carbohydrate metabolizing enzyme that acts on the 1–4 associated α-glucose residues. The inhibition of α-glucosidase slows down the process of carbohydrate digestion and avoids postprandial hyperglycemia, which is a major cause of chronic diabetes-associated complication. This study was designed to evaluate the binding capacity of isolated alkaloids with targeted receptor. For this purpose, the three-dimensional tertiary structure of the α-glucosidase was generated by using the Molecular Operating Environment (MOE). The generated model was then validated by using the RAMPAGE and ERRAT server. The molecular docking of 37 alkaloids along with standard acarbose and miglitol reported as a α-glucosidase inhibitor was performed via MOE-Dock implemented in MOE software to find the binding modes of these inhibitors. The results showed that compound 17 (oriciacridone F) and 24 (O-methylmahanine) demonstrated marked interaction with active residues and were comparable to standard inhibitors. In short, this study provided computational background to the reported α-glucosidase inhibitors and thus further detail studies could lead to novel effective compounds.
α-Glucosidase is a primary carbohydrate digestive enzyme, which is present in the brush border of the small intestine. It has action on 1,4-α bonds and thus different from β-glucosidase (1–4)1. α-Glucosidase catalyzes starch and disaccharides to glucose. Maltase is a similar enzyme that acts upon maltose and is nearly equivalent in function to α-glucosidase. The carbohydrates need metabolism by α-glucosidase before being absorbed into the small intestine. By inhibiting the α-glucosidase, the process of carbohydrate digestion slows down, which helps prevent postprandial hyperglycemia because postprandial hyperglycemia is a major cause of chronic diabetes and associated complications (5). In this regard, several research groups have been working on the desiging of new effective α-glucosidase inhibitors that can be used as therapeutic agents for the suppression of metabolic disorders such as hyperglycemia, obesity, and non-insulin-dependent type II diabetes mellitus (5).
The therapeutic potential of alkaloids has been recognized in the treatment of various human disorders (6–11). The literature review revealed that approximately 37 isolated alkaloids have been tested for α-glucosidase inhibitory activity (12), as shown in Table 1. Gao and colleagues isolated two compounds 1–2 from the leaves of Adhatoda vasica Nees. Both these compounds caused marked competitive α-glucosidase inhibition in animal models (13). The phytochemical studies of Campanulaceae Lobelia species led to the isolation of 10 compounds 4–12. These compounds also possessed significant anti-glucosidase effect (14). The potent inhibitors, deoxynojirimycin (DNJ) and 2,5-bis(hydroxymethyl)-3,4-dihydroxypyrrolidine (DMDP) (14–18), were isolated from many plants. The DNJ, along with several other therapeutic effects, provoked outstanding attenuation on glucosidase and thus clinically used as a zero-harm-antidiabetic drug agent. Three more alkaloids named piperumbellactams A–C 13–15 have been isolated from Piper umbellatum, produced significant α-glucosidase inhibition (19). Wansi et al. isolated acridones alkaloids 16–18, from Oriciopsis glaberrima Engl, also displayed profound α-glucosidase inhibition, especially compound 17 (oriciacridone F) with IC50:34.05 mM (20). Buthus martensii Karsch led to the isolation of 19, a potent non-competitive glucosidase inhibitor (21). Similarly, Piper sarmentosum led to the purification of two chaplupyrrolidones alkaloids A 20 and B 21, which possessed strong anti-glucosidase activity (22). Murraya koenigii guide to the isolation of six different alkaloids 22–27 that caused α-glucosidase inhibition. Of the compounds, O-methylmahanine 24 showed marked effect with IC50 29.1 μM (23). Tabussum and co-worker isolated plicatanins A–D 28–31 alkaloids from Chrozophora plicata also caused significant α-glucosidase inhibition (24). Six alkaloids 32–36 with potent α-glucosidase inhibitory activity have been isolated from Morus atropurpurea (12).
The aim of this research study was to find out the interaction of these reported alkaloids with the target protein and thus findings could be useful for the discovery of new, potent, and active α-glucosidase inhibitors.
Materials and Methods
In this research studies, we have generated the three-dimensional structure of the glucosidase by using the Molecular Operating Environment (MOE) software, and molecular docking study was performed on the same software. The MOE-Dock was used as docking software implemented in MOE, and ligplot is implemented in MOE for the purpose to visualize the interaction between protein and ligand.
Retrieval of the Target Sequence
The primary sequence of the α-glucosidase of Saccharomyces cerevisiae (Baker’s yeast) was retrieved using Uniprot (Universal Protein Resource)2 in FASTAformat, and the target sequence was then kept in the text file for further evaluation. The accession number of α-glucosidase of S. cerevisiae is P07265.
The target sequence of α-glucosidase was downloaded from the Universal Protein Resource (uniprot dataset). Then, Protein-BLAST (25) was done to identify homologs in the PDB (RCSB Protein Databank) (26). Hence, the crystal structure of Isomaltase from the S. cerevisiae (Pdb Id: 3A47−A), which has 72% sequence identity to the target protein, was selected as the template for the target protein sequence for the prediction of the tertiary structure of target protein.
Alignment of the Target-Template Sequence
For the sequence alignment of the target protein, α-glucosidase and template protein (PDB ID: 3A47−A), multiple sequence alignment (MUSCLE) was employed (27) server.3 The ClustalW program from the MUSCLE server was used for the alignment of the target-template sequence.
The amino acid sequence of the target protein in FASTA format was copied and paste in the sequence editor of the MOE software. Then, the template protein was loaded in the same MOE software. The chain 1 showed the target protein sequence, and chain 2 showed the template protein sequence. The target and template sequences were aligned before starting the homology modeling and calculated the root mean square deviation (RMSD) with the template. In model refining tool, the intermediate was set to medium, final model to medium, by means of scoring function generalized born/volume integral (GB/VI). Amber 99 with Solvation RField was used as a force field. Various 10 models were formulated, while the final refine model was introduced to MOE main window.
Validation of Modeled Structure
Active Site Prediction
The α-glucosidase protein active sites were studied by means of the “MOE-Site Finder” Module, which computes the possible recognition sites from the 3D atomic coordinates of the protein. The Site Finder module is considered a geometric method, as energy models were not utilized. Rather, the relative positions and accessibility of the protein atoms were targeted followed by a rough classification of chemical types. Once these regions were calculated, dummy atoms were assigned to these sites and later used to make the molecular docking calculation for specified sites.
The compounds included in our study were all collected from reported literature (12, 23). All these compounds were generated by using the Chembio-Office 2010–2012 and then all these compounds were saved in mol file for the purpose to open these files in MOE and were energy minimized via MOE using default parameters.
The modeled structure of the target protein was 3D protonated and then energy minimization was performed by using the MOE software with default parameters.
Molecular docking was performed via MOE-dock with most of the default tools with the aim to find the binding interaction of the ligand with the target protein. Ligand was docked into the target site of predicted homology model of the α-glucosidase by mean of MOE-Dock module (v.2011.10), for each ligand 10 conformations were generated. The top-ranked conformation of each ligand was used for detailed study of binding mode.
Calculation of Physiochemical Properties
For calculating the physiochemical properties, we used the Expasy-ProtParam server tool. The protein has 584 numbers of amino acids, and its estimated molecular weight was 68,183.3 Da and Theoretical pI: 5.53. The extinction coefficient (EC) of the predicted model was 148,990 at 280 nm, which indicated that at a specific wavelength, how much light was absorbed, EC is in units of m cm−1, measured in water at 280 nm. The instability index (II) was computed to be 30.07, which showed the protein was stable. The II more than 40 rated protein as not stable. The hydrophilic character was calculated by the grand average of the hydropathy index value of −0.676, and the aliphatic index was calculated to be 64.28.
The MUSCLE server was used for the determination of the alignment of the query sequence to the template. The alignment was made in order for the development of a resulting model. The configuration is presented in Figure 1. In the figure, (*) symbol represents the single entire conserved residues, (-) symbol represents the deleted regions, and (:) and (:) symbols represent the conservation of strong and weak groups correspondingly. Finally, from the evaluation of the results of target-template alignment, it was found that there is sequence homology between α-glucosidase and crystal structure of Isomaltase from S. cerevisiae 3A47–A.
For 3D structure modeling, MOE software (MOE 2010–2011) was employed, while used relative protein structure modeling in the following way.
(1) MOE docked the initial partial geometry of target sequence using template structure and used to preserved residue identity.
(2) The residues without specific backbone coordinates were characterized via a specific logic insertions and deletions treatment (30).
Model was developed while using various tools such as Model Scoring to GB/VI test (33). Force fields to Amber99 used in MOE suggested for protein homology purposes (34). Subsequent to homology modeling, the force field AMBER99 was used to minimize the energy of target structure to 0.05 G and this specifically characterized proteins and nucleic acids. The PDB format was used for resulting structure (Figure 2) having an appropriate identity. The model proposed was superimposed on template structure holding RMSD of 0.639 observing close homology (Figure 3) using the MOE software. The superposition of the target and template are shown in Figure 4.
Validation of Modeled Structure
RAMPAGE server explained the stereochemical characters of the 3D structure. Stereochemical evaluation of backbone Phi and Psi dihedral angles (35) is shown in Figure 5. Besides, Ramachandran plot analysis showed that 83.8% components were in the favored region, 10.3% residue in the permissible region, while 5.8% residues in the outlier regions of Ramachandran plot, which indicated that the proposed model is reliable for further studies. The ERRAT server explained the statistics of non-bonded interaction between different atoms, and a score of 50 was generally suitable and for the 3D structure evaluation, the predicted model had quality score 79.167, which indicated that the model was reliable and stable, as shown in Figure 6.
Figure 5. Ramachandran maps of α-glucosidase produced by RAMPAGE. Light orange and light blue are allowed regions, while dark orange and dark blue are favored regions.
Figure 6. ERRAT server shows the overall quality of the α-glucosidase. *On the error axis, two lines are drawn to indicate the confidence with which it is possible to reject regions that exceed that error value. **Expressed as the percentage of the protein for which the calculated error value falls below the 95% rejection limit. Good high resolution structures generally produce values around 95% or higher. For lower resolutions (2.5–3 A), the average overall quality factor is around 91%.
Active Site Residues
The Site-Finder Module was utilized for prediction of the ligand-binding site in the predicted model of α-glucosidase showed that GLN66, MET69, ASP106, ILE109, ASN152, ASN153, TRP154, LYS155, SER156, PHE157, PHE158, LEU174, ARG175, ARG212, ILE213, THR215, ALA216, PRO226, ILE230, LYS233, LYS236, LEU237, GLN238, HIS239, TRP242, VAL274, GLU276, VAL277, PHE300, VAL303, GLU304, THR307, SER308, PRO309, PHE310, PHE311, ARG312, TYR313, ASN347, ASP349, GLN350, ASP408, ASN412, LEU437, and ARG439 were found in the binding site of the predicted model of the α-glucosidase, as shown in Figure 7.
Figure 7. Predicted binding pocket of α-glucosidase by mean of Molecular Operating Environment Site Finder.
Binding Interaction of Ligands with Target Receptor
In our research studies, we used the 37 known alkaloid inhibitor of α-glucosidase from the previous literature. These known alkaloid inhibitors were tested and proved experimentally from the previous literature (12, 23). In the present research work, we found out the binding interaction and docking scores of these selected compounds with the target protein by molecular docking, as shown in Table 1. These results might be beneficial in the drug designing of the novel and potent inhibitors of the glucosidase.
Compound 17 and compound 24 showed the best docking score i.e., −15.1310 and −14.9192, respectively, among the 37 different alkaloids, and these compounds have good inhibition and docking score nearly similar relative to the reference (standard) ligands, miglitol (−15.4423) and acarbose (−14.7983). These two compounds are most active and showed good interaction with the target protein.
Compound 17, the most active ligand, formed three hydrogen bonds, one hydrophobic interaction, and one arene cation interaction with the Asn153, Arg312, Glu304, Trp154, and Lys155 active amino acid residues, respectively. Lys155 formed an arene cation interaction with the benzene ring of the phenol moiety of the ligand. Glu304 was observed making a hydrogen bond with the hydrogen atom of the OH group of another phenol group of the same ligand. Arg312 and Asn153 formed hydrogen bonds with the oxygen atom double bonded with the piperidine moiety of the ligand and oxygen atom of −OH moiety of the phenol of dihydroxy-3,3-dimethyl-1,2,3,4-tetrahydrobenzo[c]acridin-7(12H)-one, respectively, of the same inhibitor. Trp154 showed a hydrophobic interaction with the H atom of the −OH group of the dihydroxy-3,3-dimethyl-1,2,3,4-tetrahydrobenzo[c]acridin-7(12H)-one moiety. The 3D interaction of the ligand with receptor was shown in Figure 8. Similarly, these results were in absoulte agreement with the in vitro α-glucisade inhibitory activity already reported. Moreover, it also caused marked free radical scavenging effect (20). Compound 24 is the second most active ligand and interacted with the Asn153 and Lys233 and was observed making three hydrogen bonds. Asn153 formed H-bonds with the hydrogen atom of OH group and with the oxygen atom of another −OH group of the same ligand. Lys233 was observed making an H-bond (hydrogen bond) with the −O atom (oxygen atom) of the hydroxyl moiety of the inhibitor, as shown in Figure 9. The docking results are consistant with the in vitro α-glucisade inhibitory activity already reported, agumented by its comprehensive antioxidant effects (23).
Compound 37 has moderate good docking score −10.4884 and have the best interaction with active residues. It formed five hydrogen bonds with the Asn153, Lys155, Lys233, Glu276, and Asn347, a hydrophobic interaction with the Asp349 and arene cation interaction with the Arg312. Arg312 made an arene cation interaction with the phenylene moiety of the ligand. Lys155 and Glu276 formed hydrogen bonds with the oxygen atom and hydrogen atom of the butane-1-ol. Asn153, Asn347, and Lys233 formed hydrogen bond interactions with the oxygen atom of the hydroxyl group (−OH) of the butane-4-ol. Asp349 formed ahydrophobic interaction with the hydrogen atom of the −OH group of the butane-2-ol moiety of 1,1′-(1,4-phenylene)-bis(butane-1,2,3,4-tetraol) shown in Figure 10.
Compound 33 had low docking score −5.8070 and showed a low number of interaction with the active residues, i.e., formed one hydrogen bond and one hydrophobic interaction with the Lys155, as given in Figure 11. Lys155 made a hydrogen bond with the oxygen atom of OH group, and Lys155 interacted with the hydrogen atom of another −OH moiety of the (2R,3R,4R)-2-(hydroxymethyl)piperidine-3,4-diol. Figure 12 showed the two-dimensional interaction images of the compounds with the target protein.
Figure 12. The figure shows the 2D images of the docked conformations of the ligands with the active residues (A) 2D image of compound 17, (B) 2D image of compound 24, (C) 2D image of compound 37, and (D) 2D image of compound 33.
The molecular docking was made to recognize the binding interactions of these reported compounds with the receptor. We examined the interaction of inhibitors to that of our target receptor. The molecular docking study indicates good docking score and binding mode and thus showed therapeutic potential of these compounds on α-glucosidase inhibition. Compound 17 (oriciacridone F) and 24 (O-methylmahanine) demonstrated marked interaction with active site residues, which are also correlated with the reported IC50 values and, thus, might be the best candidates for the discovery of novel α-glucosidase inhibitors, after in vivo efficacy, safety, and clinical studies.
Moreover, the rest of alkaloids with good receptor interaction could be lead compounds and therefore need further studies in terms of synthesis, structural relationship activity followed by testing in various in vitro and in vivo testing.
MZ, AK, and ML carried out the in silico studies and initial draft of the manuscript. AR assisted in molecular docking of test compounds. HK supervised the entire study and finalized the draft.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: α-glucosidase inhibitors, homology modeling, molecular docking, Molecular Operating Environment, α-glucosidase
Citation: Zafar M, Khan H, Rauf A, Khan A and Lodhi MA (2016) In Silico Study of Alkaloids as α-Glucosidase Inhibitors: Hope for the Discovery of Effective Lead Compounds. Front. Endocrinol. 7:153. doi: 10.3389/fendo.2016.00153
Received: 08 August 2016; Accepted: 23 November 2016;
Published: 19 December 2016
Edited by:Undurti Narasimha Das, UND Life Sciences, USA
Reviewed by:Rade Vukovic, Mother and Child Health Care Institute of Serbia, Serbia
Priyanka Agarwal, Cedars-Sinai Medical Center, USA
Copyright: © 2016 Zafar, Khan, Rauf, Khan and Lodhi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Haroon Khan, email@example.com