Open AccessArticle

Characterization of Umami Dry-Cured Ham-Derived Dipeptide Interaction with Metabotropic Glutamate Receptor (mGluR) by Molecular Docking Simulation

Alejandro Heres

Fidel Toldrá

and

Leticia Mora

Instituto de Agroquímica y Tecnología de Alimentos (CSIC), Avenue Agustín Escardino 7, 46980 Paterna, Spain

Author to whom correspondence should be addressed.

Appl. Sci. 2021, 11(17), 8268; https://doi.org/10.3390/app11178268

Submission received: 13 July 2021 / Revised: 31 August 2021 / Accepted: 2 September 2021 / Published: 6 September 2021

(This article belongs to the Special Issue Role and Properties of Proteins and Peptides in Foods)

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Abstract

Dry-cured ham-derived dipeptides, generated along a dry-curing process, are of high importance since they play a role in flavor development of dry-cured ham. The objective of this study was to analyze the residues of the less-studied metabotropic glutamate receptor 1 (mGluR1) implicated in the recognition of umami dry-cured ham dipeptides by molecular docking simulation using the AutoDock Suite tool. AH, DA, DG, EE, ES, EV, and VG (and glutamate) were found to attach the enzyme with inhibition constants ranging from 12.32 µM (AH) to 875.75 µM (ES) in the case if Rattus norvegicus mGluR1 and 17.44 µM (VG) to 294.68 µM (DG) in the case of Homo sapiens, in the open–open conformations. Main interactions were done with key receptor residues Tyr74, Ser186, Glu292, and Lys409; and Ser165, Ser186, and Asp318, respectively, for the two receptors in the open–open conformations. However, more residues may be involved in the complex stabilization. Specifically, AH, EE and ES relatively established a higher number of H-bonds, but AH, EV, and VG presented relatively lower Ki values in all cases. The results obtained here could provide information about structure and taste relationships and constitute a theoretical reference for the interactions of novel umami food-derived peptides.

Keywords:

dry-cured ham; dipeptides; flavor; umami: mGluR1

1. Introduction

Dry-cured ham is a high added-value product consumed worldwide [1,2]. The European Union recognizes a broad variety of different dry-cured ham types, half of which are classified as protected designation of origin and half classified as protected geographical indication [3], due to the particular pig breed and processing conditions that influence the final texture and flavor characteristics of the product. The dry-curing process is crucial for the quality of the product, which is conditioned by a wide range of factors such as animal feedstuffs, raw material and pork genetics, age, sex, and processing conditions, since they have an effect on the biochemical reactions that arise from the post-mortem stage [3,4,5,6,7,8]. Proteolysis and lipolysis are two of the main biochemical reactions contributing to the organoleptic properties. The endogenous exopeptidases and endopeptidases cleave muscle proteins, mainly myofibrillar and sarcoplasmic proteins, leading to the release of high amounts of short peptides and amino acids by which the sensory profiles of dry-cured ham are strongly affected [9,10]. Many peptides generated in dry-cured ham have been identified and characterized, some of which exert a wide range of bioactivities [11]. However, little is known about their role as taste-active compounds. In this line, size-exclusion peptide fractionation demonstrated that bitterness was perceived in the earlier-running fractions of molecular mass, around 1700 Da, followed by savory and salty taste from 1700 to 1500 Da. Umami and “brothy” tastes were perceived below 1500 Da, and finally bitter taste was found again due to the presence of Y and hypoxanthine amino acids. Hydrolysis of the savory fractions showed that G, K, S, taurine, T, A, P, Y, V, M, I, and L amino acids were the most abundant in comparison with the lowest levels of C amino acid/cystine. The hydrolyzed umami and brothy fraction revealed a high content in F amino acid, whose bitter taste was (pointed out to be) masked by the levels of E, S, G, H, A, M, and K amino acids [12]. Precisely, it was discovered that the response to bitterness can be suppressed by acidic dipeptides EE, DD, and amino acids E and D [13]; in agreement with umami peptides ED, EE, ES, DES, and EGS, they also behave as bitterness suppressors [14]. In another study with a similar methodology, fractions below 1200 Da were related with sour, bitter, and salty tastes, in joint, with brothy and dry-cured ham typical aromatics. It was also found that those tastes discovered in some fractions may be due to the presence of dipeptides, such as VE, IV, LE, ID, AM, GE, ER, PL, GS, DV, and SK [15]. These findings constitute interesting results about the relation of the peptide size and flavor, as well as the potential flavor characteristics of some dipeptides, but there are still limited data about the specific taste, which is imparted by isolated peptides. Data obtained from in silico simulations provide insight into the potential taste and interaction mechanism with the taste receptors. Examples of studies following molecular docking allowed the discovery of pharmaceutical and bioactive compounds [16], such as SFGYVAE, a potent inhibitory peptide for 3-hydroxy-3-methylglutaryl CoA reductase [17]; molecules approved in phase-I clinical trials to identify 3CL protease inhibitors to treat COVID-19 [18]; or a methodology for developing new neuroprotective drugs from traditional Chinese medicine, which target metabotropic umami receptors (mGluRs) [19], demonstrating that in silico analyses streamline the empirical research. Indeed, the details obtained from database searches can be used for the formation of a data matrix when constructing a quantitative structure–activity relationship biostatistical model, and for molecular docking to predict the potential taste of unknown peptides by estimating the receptor’s residues involved in the interaction and the binding affinities [20,21].

Specialized taste receptor cells harbor G protein-coupled receptors (GPCRs), whose signalization when binding to umami substances is transmitted to gustatory afferent fibers via ATP signaling [22,23]. To date, the known umami receptors are T1R1/T1R3, expressed in the taste cells of the lingual epithelium and in the gut [24], mGluR4, also expressed in the brain [25], and mGluR1, also widely expressed throughout the central nervous [26] and in the stomach [27]. Although the heterodimer receptor T1R1/T1R3 was identified as one of the most firmly established umami receptors [28], intriguingly, knockout mice lacking the Tas1r1 or Tas1r3 gene sequences showed only partial taste loss for the umami taste, evidence arguing that mGluR1 receptors can also contribute to the umami taste [26,29,30]. Unfortunately, a structure of T1R1/T1R3 has not been published to date, and while homology models based on mGluR1 atomic coordinates have been used for the study of T1R1/T1R3 interactions with umami compounds, less is known about how mGluR1 recognizes such taste-active molecules.

The present work is aimed to, in silico, predict the interactions, by using Rattus norvegicus and Homo sapiens mGluR1 receptors, the latter more recently disclosed, with umami dry-cured ham-derived dipeptides recently identified, and which could have a key role in the development of dry-cured ham flavor. The findings obtained here would serve as a reference for potential mGluR1-interacting peptides susceptible to imparting the umami taste, as well as serve as a theoretical insight into the umami-contributing peptide sequences.

2. Materials and Methods

The dipeptides AH (PubChem ID: 9837455), DA (PubChem ID: 5491963), DG (PubChem ID: 151148), EE (PubChem ID: 439500), ES (PubChem ID: 6995653), EV (PubChem ID: 6992567), VG (PubChem ID: 6993111), which have been described as taste-related peptides and are present in dry-cured ham, were processed for an in silico analysis in order to predict their potential interacting mechanisms with the receptor. The ligand sequences, as well as that from glutamate (E) (PubChem ID: 33032), were obtained in “sdf” format from PubChem tool (https://pubchem.ncbi.nlm.nih.gov/, accessed on 15 July 2021) [31], and the PDB files were extracted using Discovery Studio Visualizer v20.1.0.19295 software (Dassault Systèmes BIOVIA Corp., 2020). The structures of mGluR1 Rattus norvegicus closed–open and open–open conformations, and Homo sapiens open–open conformation (protein data bank ID: 1EWK, 1EWT and 3KS9), in complex with E [32], ligand free and LY341495 antagonist [33], respectively, were downloaded from the Protein Databank (PDB) tool (https://www.rcsb.org/, accessed on 15 July 2021) [34].

Ligand-protein docking simulations were carried out using AutoDock v1.5.6 and AutoDock v4.2.5.1 (Scripps Research Institute) software [35,36]. The minimum system requirements are Intel 32/64-bit, Pentium/Dual core, Microsoft Windows (98, 2000, XP, Vista, Windows 7)/Linux and Macintosh, 256 MB of minimum RAM, and 200 MB of minimum hard disk space.

Gasteiger charges and hydrogens were added to all molecules; water molecules and original ligands were also removed from the enzyme, and ligand torsions were detected by AutoDock. Structure data files were converted into the Protein Data Bank partial charge and atom type format.

Firstly, a preliminary test to obtain more information about the coordinates of the area for screening was carried out. Insights were made by submitting the original receptor PDB archives to ProteinsPlus, and processing the molecule with the tool PoseView (https://proteins.plus/, accessed on 15 July 2021) [37,38] and the web server DoGSiteScorer (https://proteins.plus/, accessed on 15 July 2021) [39].

The definitive Grid Box (60 × 60 × 60) was centered on one of the mGluR1 binding sites where active residues located, with coordinates X = 11,407, Y = 13,031, and Z = 12,342 for 1EWK [40,41], X = 16,958, Y = 28,615, and Z = 45,202 for 1EWT and X = -41,815, Y = 9,345 and Z = 34,170 for 3KS9 [42], with a spacing of 0.375 Å. Fifty docking runs were performed, using a Lamarckian genetic algorithm between the flexible ligand and rigid receptor, a population size of 150, a maximum of 2,500,000 generations and 2,500,000 evaluations for 50 GA runs. The root-mean-square deviation tolerance was set to 2.0 Å for the clustering of docking results. Analysis of the results were conducted by sorting the different complexes with respect to the predicted binding energy. The pose with the lowest binding energy in each case was individually examined, and interactions were processed with online software, Protein–Ligand Interaction Profiler (PLIP) (https://plip-tool.biotec.tu-dresden.de/plip-web/plip/index, accessed on 15 July 2021) [43], to validate the interactions; and with ProteinsPlus (https://proteins.plus/, accessed on 15 July 2021) [37,44] to obtain the two-dimensional representations by using the PoseView algorithm [44].

3. Results and Discussion

Dipeptides in dry-cured ham are mainly generated by dipeptidyl dipeptidases (DPPs) and by the progressive shortening of longer peptides by other endogenous enzymes. It has been shown that DPPs release dipeptides from the N-terminal of peptide fragments [45], and despite their substrate specificities, all of them are able to release other dipeptides at lower rates [46].

Short peptides are in the limit of some standard proteomic approaches due to their small sizes and signal inhibition, due to matrix interactions in the mass spectrometers [45,47,48]. Considering the high probability of the dipeptides sequence being represented in a wide variety of proteins, the profiling, structural estimation, quantification, and identification using traditional procedures based on matching the m/z spectrum with theoretical peptide sequences using databases is not feasible [49,50]. In fact, the de novo interpretation of the fragmented spectra by experienced personnel is frequently needed [48], which is a time-consuming and complex task. Thus, peptidomic approaches based on prior chromatographic steps have been developed to concentrate and isolate those peptides of interest. As a result, umami dipeptides AH, DA, DG, EE, ES, EV, and VG, described in Table 1, have been successfully detected in dry-cured hams. In fact, the dipeptide AH has been identified in Jinhua ham with a relative peak area percentage of 3.40, by size-exclusion chromatography (SEC)-reverse-phase high performance liquid chromatography (RP-HPLC) coupled with MALDI SYNAPT-multiple monitoring reactions (MRM)-Q-ToF mass spectrometry [51,52,53].

3.1. Rattus Norvegicus and Homo sapiens mGluR1s Shared Homology

The aim of this work was to estimate the interactions between mGluR1 and umami dipeptides found in dry-cured ham. These findings, in joint with peptidomic and further sensory analysis, will provide interesting evidence about the development of dry-cured ham flavor by the generation of short peptides, and will contribute to predict the taste of unknown peptides present in foods. As the Homo sapiens mGluR1 crystal structure (PDB ID: 3KS9; UniProt ID: Q13255) was recently resolved, and there is little information about its mechanism, a first comparative study with the most frequently employed Rattus norvegicus mGluR1 (PDB ID: 1EWK; UniProt ID: P23385) was conducted. Figure 1 indicates an alignment [57] of both FASTA sequences.

As presented in Figure 1, an identity of 94.01% was estimatedbetween Rattus norvegicus mGluR1 (PDB ID: 1EWK) and Homo sapiens mGluR1 (PDB ID: 3KS9). Only a few mismatches were found at positions apparently not belonging to key residues of the binding site, suggesting that the motif is evolutionarily conserved [58].

Based on their signal transduction pathways and pharmacological properties, mGluRs have been categorized into three groups: Group I (mGluR1 and mGluR5) are normally stimulatory and associated with phospholipase C activation and second messengers, such as inositol and diacylglycerol production. Group II (mGluR2 and mGluR3) and Group III (mGluR4, mGluR6, mGluR7, and mGluR8) normally inhibit glutamatergic neurotransmission and they are both negatively coupled to adenylyl cyclase [59]. The N terminus of mGluRs comprises a large extracellular E-binding domain and the cytoplasmic C terminus of mGluRs participates in interactions with G proteins [25]. The taste receptor mGluR1 has been found in rat circumvallate and foliate papillae of the posterior tongue, in a truncated form compared to its homologous expressed in the brain. Its activation depends on the disulfide-linked homodimer conformation, and signalization probably occurs through IP3 formation and Ca2⁺ release from intracellular stores, but only at concentrations ≥1 mmol E [60]. The bi-lobed protomer architectures flexibly change their domain arrangements to form an “open” or “closed” conformation. Upon agonist binding, the protomer is closed at the cleft between the two ligand-binding sites, conformations, which are referred to as closed and open forms. However, the actual conformation in the physiological state is still unknown [61]. To our knowledge, there is only a structure linked to the Human mGluR1 determined, with an open–open conformation (PDB ID: 3KS9), while the most studied Rattus norvegicus mGluR1 structure published to date consists of a closed–open conformation (PDB ID: 1EWK). Other structures from this last publication are an open–open conformation (PDB ID: 1EWT) and a closed–open conformation in the ligand free form (PDB ID: 1EWV) [61,62]. For these reasons, this work strives to bring to light the receptor residues implicated when mGluR1 adopts the active closed–open conformation and, at the same time, perform a comparative study between both open–open forms of mGluR1 belonging to the Rattus norvegicus and Homo sapiens.

In the case of the more studied Rattus norvegicus mGluR1 (PDB ID: 1EWK), the active residues are described to be Tyr74, Arg78, Ser164, Ser165, Ser186, Thr188, Asp208, Tyr236, Glu292, Gly293, Asp318, Arg323, and Lys409 [40,41]. Otherwise, the Homo sapiens mGluR1 active residues belonging to the active site have been predicted to be Trp110, Gly163, Ser164, Ser165, Ser186, Tyr236, Asp318, Asp319, Ala329, and Gly379 [42]. Thus, both receptors were evaluated in order to obtain a more accurate prediction.

The dipeptides AH, DA, DG, EE, ES, EV, VG, and glutamic acid (positive control) were studied through molecular docking analyses to understand their possible mechanism of interaction with the umami receptor mGluR1.

3.2. Interaction between Umami Dipeptides and Rattus Norvegicus mGluR1 Closed–Open Conformation

As shown in Table 2 and Figure 2, the estimated interacting residues, binding type, and binding energy of interactions are calculated in this in silico process. It is important to remark that the figures, used for a simpler overview of the dockings, represent two-dimensional interactions obtained from PoseView tool, which estimates the interactions between the complex partners by using simple geometric criteria, such as distances and angles [63]. Thus, not all interactions are drawn.

Rattus norvegicus mGluR1 key receptor residues from the closed–open conformation, Tyr74, Ser165, Ser186, Thr188, Asp318, Arg323, and Lys409 were predicted to interact with E (Ki = 15.58 µM). With respect to the dipeptide AH (Ki = 8.26 µM), the key residues Tyr74, Arg78, Ser186, Tyr 236, Glu293, Arg323 and Lys409 would be implicated. DA (Ki = 27.24 µM) was calculated to interact with Tyr74, Ser165, Thr188, Tyr236, Glu292, Gly293, Asp318, Arg323, and Lys409, while DG (Ki = 6.0 µM) would react with Tyr74, Arg78, Ser165, Ser186, Thr188, Tyr236, Asp318, and Lys409. On one hand, EE (Ki = 59.42 µM) could bond with Tyr74, Arg78, Ser165, Ser186, Thr188, Glu292, Gly293 Arg323, and Lys409. On the other hand, ES (Ki = 9.17 µM) would be able to form connections with Tyr74, Arg78, Gly293, Asp318, Arg323, and Lys409. EV (Ki = 7.87 µM) was estimated to dock between Tyr74, Glu292, Gly293, Asp318, Arg323, and Lys409. Finally, VG (Ki = 811.24 nM) would bind to Tyr74, Arg78, Ser186, Thr188, and Lys409. Nevertheless, it is important to consider that non-key residues may participate in the stabilization, such as with Trp110, for the case of AH, EE, ES, and EV.

Otherwise, residues, such as Arg323 and Lys409, can make interactions of different nature, as they can stablish H-bonds, hydrophobic forces, or even salt bridges. The majority of the interactions are of H-bond nature, even various with the same residue, such as with Tyr74, Ser165, or Arg323. The dipeptide EE, followed by ES, established the largest number of H-bonds, suggesting the presence of an E residue particularly promotes docking with the receptor in comparison with the other dipeptides. In addition, the nature of the C-terminal of these three dipeptides may provide insights on a polar side chain residue benefits the contact with the receptor. The number of hydrophobic interactions and salt bridges appear very similar between them for each dipeptide, except for glutamic acid, which could not form hydrophobic interactions by itself. Finally, the lowest Ki values were those from VG then DG followed by EV and AH.

3.3. Interaction between Umami Dipeptides and Rattus Norvegicus mGluR1 Open–Open Conformation

Table 3 and Figure 3 are presented hereunder, outlining the interactions in this case.

Glutamic amino acid E (Ki = 694.05 µM) was revealed to stabilize bonds with Rattus norvegicus mGluR1 key receptor residues from open–open conformation Tyr74, Arg78, Ser186, and Lys409. Tyr74, Arg78, Ser165, Ser186, Thr188, and Lys409 were calculated for the case of the dipeptide AH (Ki = 12.32 µM). The dipeptide DA (Ki = 322.75 µM) would interact with key residues Tyr74, Glu292, and Lys409; while DG (Ki = 424.75 µM), with Tyr74, Arg78, Ser186, Arg323, and Lys409. E-containing dipeptide EE (Ki = 27.93 µM) was predicted to link to Tyr74, Arg78, Ser186, Glu292, and Lys409; whereas ES (Ki = 875.75 µM), with Tyr74, Ser186, Asp318, and Lys409; and EV (Ki = 29.93 µM) with Tyr74, Glu292 and Lys409. Finally, the dipeptide VG (Ki = 694.05 µM) was predicted to interact with key residues Glu292 and Tyr236. As in the previous case, more non-key residues seemed to be implicated in the stabilization of the dockings, such as Arg71 in DA, EE, EV, and VG; or Trp110 in AH, EE, ES, EV, and VG.

Receptor residues Tyr74 and Glu292 would be able to make H-bonds and hydrophobic forces, while Lys409 could form H-bonds and salt bridges in the same complex. Still, main interactions are due to H-bonds, highlighting the role of Tyr74, Ser186, and Glu292. Otherwise, the dipeptide AH, followed by ES, would make the greatest number of H-bonds, while in the case of the closed–open conformation, the peptides EE and ES reached a greater number of H-bonds. These differences may be due to the conformational changes of the receptor. Still, polar C-terminal amino acids may contribute to the establishment of H-bonds.

The number of salt bridges was greater than that of hydrophobic interactions in few cases, such as those from E and EE, while DA and DG lacked hydrophobic bonds.

The Ki values increased from AH, to EE, EV, VG, DA, DG, E, and finally, ES, which revealed that the Ki would not be benefited from the C-terminal non-polar residues, as it occurred in the closed–open conformation. As mentioned before, these differences may be due to the conformational changes, which would expose the key residues in a non-identical manner, translating it into different interactions and Ki values.

3.4. Interaction between Umami Dipeptides and Homo sapiens mGluR1 Open–Open Conformation

Results of these dockings are shown below by means of Table 4 and Figure 4.

According to Bupesh et al. (2016) [42], in the case of Homo sapiens mGluR1 open–open conformation docking, only their predicted key resides from the active site Trp110 and Ser186 would interact with E (Ki = 438.58 µM). AH could bond with Ser165, Ser186, and Tyr236. Intriguingly, it may not only stablish an H-bond with Tyr236, but also a perpendicular π-stacking interaction. With respect to DA (Ki = 92.95 µM), Ser165, Ser186, Asp318 would participate in the docking; it also happens in the case of EE (Ki = 248.83 µM), and EV (Ki = 33.23 µM). Whereas DG (Ki = 294.68 µM) could bind to Ser165 and Ser186, ES (Ki = 165.54 µM) and VG (Ki = 17.44 µM) would dock with Ser165 and Asp318. It is important to note that the repeatability of some non-key residues in all dipeptide cases, such as Thr188, Gln211, Lys409, and glutamic acid-binding residues Tyr74 and Arg78, suggest more of the previously predicted in the bibliography may be implicated in the recognition of umami compounds. Since the crystallographic structures 1EWK and 3KS9 are available in closed–open and open–open conformation states, the differences observed on residues may be due to conformational changes [64].

Apparently, residues, such as Thr188 and Tyr74, can form both H-bonds and hydrophobic interactions. However, as in the previous cases, most interactions are due to H-bonds. In fact, AH, EE, ES, and EV presented the same number of them with slightly differences in the residues implicated, which explains the diversity of Ki values and, thus, it may illustrate the receptor specificity. It seems that in the Rattus norvegicus closed–open conformation, polar acidic residues from dipeptides promote H-bonds. Salt bridges and hydrophobic connections appear to distribute differently compared to what occurred for the Rattus norvegicus mGluR1 receptor. Actually, the dipeptides AH and VG would not be able to stablish salt bridges.

Attending to the Ki, lower values were obtained for AH, EV, and VG. Making a comparison between the open–open conformations of Rattus norvegicus and Homo sapiens, the most frequent and common residues that interacted with E were Tyr74 and Lys409. This last residue is also remarkable for the case of dipeptides in joint with Ser186. However, a disparity of interactions between both receptors could be perceived, indicating that various key residues implicated in the recognition of the ligands would differ between the two species although the sequence is highly conserved. Intriguingly, considering the residues predicted for the same receptor, the majority of them are repeated for each dipeptide. Indeed, the dipeptides may attach to the Rattus norvegicus closed–open conformation by Tyr74, Trp110, Ser186, Thr188, Asp318, Arg323, and Lys409. Tyr74, Trp110, Ser186, Glu292, and Lys409 frequently appeared for the case of Rattus norvegicus open–open conformation and Ser165, Ser186, Thr188, Gln211, Asp318, and Lys409 are remarkable attending to the Homo sapiens open–open conformation.

The open–open conformations from the two species generally presented lower number of H-bonds in comparison with the closed–open conformation from Rattus norvegicus, which probably was translated in a lower Ki value range. This may be because the conformational change to the closed form that occurred in the ligand-binding domain benefited the docking within the protomer, promoting a greater number of interactions. Based on the results provided by the in silico prediction, it seems the Ki did not show a particular trend attending to the peptide sequence as the dipeptides with lower values were not similar when comparing the cases. However, VG was present as one of those with the lowest Ki in all three cases.

There is little information reporting mechanism analyses with mGluR1. In fact, most investigations are based on the use of 1EWK and 3KS9 mGluR1s as templates for homology modeling to simulate the docking between drugs or taste-active molecules and T1R1/T1R3 or T2R1/T1R3 [65,66,67,68,69,70], and do not deepen the contribution of mGluRs to taste perception, although knockout studies have demonstrated that they play a key role independently of the heterodimers in umami recognition [29].

It is known that E recognition is accomplished by Tyr74, Arg78, Ser165, Ser186, Thr188, and Lys409 in both ligand-binding regions. However, residues Ser164, Asp208, Tyr236, Glu292, Gly293, Asp318, and Arg323, in the closed subunit, are implicated [62]. Some of these interactions were found in this study in both cases, but also when docking using the dipeptides as ligands. Docking simulations between 1EWK and sweet aspartyl-dipeptide derivatives revealed similar involved residues, such as Ser186, Asp318, and Lys409 through H-bonds; Arg78, Ser186, Thr188, Asp318, and Lys409 by salt bridges and Tyr74 and Tyr236 by hydrophobic interactions. In addition, some of the derivatives were able to stablish H-bonds with Trp110 and Gln211. The carboxylate groups appear to benefit the interaction with Lys409, whereas the carbonyl group ligand derivatives, with Arg323 as benzene ring-containing derivatives can have hydrophobic interactions with residues Tyr74 and Tyr236 [40]. Eugenol, a phenolic compound found in the leaves, buds, of clove Syzygium aromaticum (L.) Merrill and Perry, links with 3KS9 with similar residues, such as Trp110, Ser165, and Asp318 [42].

Such predicted estimations obtained in this study, in agreement with others, indicate that umami dipeptides dock the mGluR1 active site by mimicking E, but other residues may be implicated in each particular dipeptide to stabilize the binding.

Briefly, it is important to remark that these dipeptides have been previously demonstrated to exert bioactive properties. Indeed, the dipeptide AH has been registered on BioPep [71] as in vitro ACE-I and DPP-IV inhibitor and in vitro antioxidant. DA and DG can act as in vitro ACE-I inhibitors; DA can also act as in vitro DPP-III inhibitor. The dipeptide EE would act as a stimulating vasoactive substance release in human aortic endothelial cells; ES exerts in vitro DPP-IV inhibitory activity and EV and VG can be in vitro ACE and DPP-IV inhibitors.

More recently, dipeptides EE, ES, and DA have been tested for their anticholesterolemic activity obtaining values of 47.2, 45.5, and 49.6% of HMG-CoA inhibitory activity, respectively, at 1 mM [72].

On the other hand, as mentioned above, mGluR1 has been found in the stomach [27]. Specifically, it has been located at the apical membrane of chief cells and possibly in parietal cells in a rat glandular stomach. A diet with 1% E amino acid in rats was reported to induce changes in the expression of pepsinogen C and gastric intrinsic factor mRNAs in stomach mucosa [73], which suggests that mGluR1 is involved in the gastric phase regulation of protein digestion [74]. Other genes affected by E supplementation were serotonin receptor 3A (Htr3a), nitric oxide synthase 3 (Nos3), phospholipase type C-β1 (Plcb2), and transient receptor potential cation channels Trpc1 and Trpm5. The last three are related to the mGluR1 signal transduction cascade [73].

In addition, activation of mGluR1 modulates gastric vagal afferents from the luminal side, releasing mucin and nitrite mono-oxide, which stimulates serotonin (5HT) release at the enterochromaffin cell. Finally, this 5HT stimulates 5HT3 receptor at the nerve end of the vagal afferent fiber. Besides, studies in rats revealed that luminal E amino acid signaling contributes to control digestion and thermogenesis without obesity [75].

Thus, E amino acid-like tasting compounds, such as the dipeptides of this study, which are produced during the processing of dry-cured ham, might act as multifunctional agents, activating these responses by interaction with stomach mGluR1 [76].

4. Conclusions

The mGluR1 residues implicated in the recognition of E amino acid and umami dry-cured ham-derived dipeptides AH, DA, DG, EE, ES, EV, and VG, were, in silico, predicted through the use of Rattus norvegicus and Homo sapiens mGluR1 receptors for molecular docking. Results suggested that key residues from the binding site interact with E and dipeptides. However, other non-common residues may stabilize the dipeptide complex. Although differences in the residues implicated have been observed between mGluR1 of Rattus norvegicus and Homo sapiens, the most relevant residues were predicted to be Tyr74 and Lys409 for the recognition of E; and Ser186 and Lys409 for the docking of the dipeptides, being able to establish more than one bond and of different nature. Globally, AH and E-containing dipeptides seemed to make a greater number of H-bonds. In addition, no trend was detected when analyzing the Ki values, but VG was one of those presenting the lowest values. Finally, it is important to note that these umami compounds may play a role in digestion control and thermogenesis via stomach mGluR1. The results obtained here could provide information about sequence and taste relationships, and constitute a theoretical reference for the interactions of novel umami food-derived peptides.

Author Contributions

Conceptualization, A.H. and L.M.; methodology, A.H. and L.M.; formal analysis, A.H.; resources, L.M. and F.T.; writing—original draft preparation, A.H.; writing—review and editing, A.H., L.M. and F.T.; supervision, L.M. and F.T.; funding acquisition, L.M. and F.T. All authors have read and agreed to the published version of the manuscript.

Funding

Grant AGL2017-89381-R and FEDER funds from the Spanish Ministry of Economy, Industry and Competitiveness, and Ramón y Cajal postdoctoral contract RYC-2016-19635 by L.M. are acknowledged.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are contained within the article.

Acknowledgments

The proteomic analysis was performed in the proteomics facility of SCSIE University of Valencia that belongs to ProteoRed, PRB3 and is supported by grant PT17/0019, of the PE I+D+i 2013-2016, funded by ISCIII and ERDF.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

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Figure 1. Alignment analysis of protein sequences between Rattus norvegicus mGluR1 (PDB ID: 1EWK; UniProt ID: P23385) and Homo sapiens mGluR1 (PDB ID: 3KS9; UniProt ID: Q13255). Identity: 94.01%; identical positions: 1130; similar positions: 41. Fully conserved residues are indicated with “*”; conservation between groups of strongly similar properties is labeled with “:”; a “.” indicates conservation between groups of weakly similar properties; and a blank space signifies none of the above.

Figure 2. Two-dimensional representation of protein–ligand interactions between Rattus norvegicus closed–open conformation of mGluR1 (PDB ID: 1EWK) and Glu (PubChem ID: 33032), AH (PubChem ID: 9837455), DA (PubChem ID: 5491963), DG (PubChem ID: 151148), EE (PubChem ID: 439500), ES (PubChem ID: 6995653), EV (PubChem ID: 6992567), VG (PubChem ID: 6993111). H bonds are shown as dashed lines, hydrophobic contacts are represented by green splines; the corresponding pocket residues are shown in the same color. Diagrams obtained from the ProteinsPlus PoseView tool, from which E amino acid was predicted to interact with Tyr74, Ser165, Thr188, Ser186, Asp318 and Lys409 by H-bonds; AH, with Tyr74, Ser186, Thr188, Aps318 and Lys409 by H-bonds, Trp110 by π–π stacking and a hydrophobic interaction; DA, with Tyr74, Ser165, Thr188 and Gly293 by H-bonds; DG, with Tyr74, Arg78, Ser165, Ser186, Thr188, Asp318, and Lys409 by H-bonds; EE, with Tyr74, Ser165, Ser186, Thr188, Met294, Gly319, Arg323, and Lys409 by H-bonds and Trp110 by hydrophobic interaction; ES, with Arg71, Tyr74, Arg78, Ser186, Met294, Arg323, and Lys409 by H-bonds and Trp110 by hydrophobic interaction; EV, with Arg71, Tyr74, Glu292, Gly293, Met294, Arg323, and Lys409 by H-bonds and Trp110 by hydrophobic interaction; and VG, with Tyr74, Arg78, Ser186, Asp318, and Lys409 by H-bonds.

Figure 3. Two-dimensional representation of protein–ligand interactions between Rattus norvegicus open–open conformation of mGluR1 (PDB ID: 1EWT) and Glu (PubChem ID: 33032), AH (PubChem ID: 9837455), DA (PubChem ID: 5491963), DG (PubChem ID: 151148), EE (PubChem ID: 439500), ES (PubChem ID: 6995653), EV (PubChem ID: 6992567), VG (PubChem ID: 6993111). H bonds are shown as dashed lines, hydrophobic contacts are represented by green splines; the corresponding pocket residues are also shown in the same color. Diagrams obtained from the ProteinsPlus PoseView tool, from which E amino acid was predicted to interact with Tyr74, Arg78, Ser186 and Lys409 by H-bonds; AH, with Tyr74, Arg78, Gly163, Ser186 and Lys409 by H-bonds and Ser186 by a hydrophobic interaction; DA, with Arg71 and Lys409 by H-bonds; DG, with Tyr74, Ser186, Lys409 by H-bonds; EE, with Arg71, Arg78, Ser186, Glu292 and Lys409 by H-bonds and Trp110 by hydrophobic interaction; ES, with Tyr74, Asp318 and Lys409 by H-bonds; EV, with Arg71, Tyr74 and Lys409 by H-bonds; and VG, with Arg71, and Glu292 by H-bonds.

Figure 4. Two-dimensional representation of protein–ligand interactions between Homo sapiens open–open conformation of mGluR1 (PDB ID: 3KS9) and Glu (PubChem ID: 33032), AH (PubChem ID: 9837455), DA (PubChem ID: 5491963), DG (PubChem ID: 151148), EE (PubChem ID: 439500), ES (PubChem ID: 6995653), EV (PubChem ID: 6992567), VG (PubChem ID: 6993111). H bonds are shown as dashed lines, hydrophobic contacts are represented by green splines; the corresponding pocket residues are also shown in the same color. Diagrams obtained from the ProteinsPlus PoseView tool, from which E amino acid was predicted to interact with Tyr74, Arg78, Ser186, and Lys409; AH, with Ser165, Thr188, Asp208, Asp318; DA, with Ser165, Thr188, Asp318, and Lys409; DG, with Ser165, Asp208, Asp318 and Lys409; EE, with Ser165, Thr188, Asp208, and Lys409; ES, with Ser165, Thr188 and Lys409; EV, with Ser165, Thr188, Asp208, Asp318, and Lys409; and VG, with Ser165, Thr188, Asp208, and Asp318. H-bonds were estimated by PoseView to be stabilized in all cases.

Table 1. Main physicochemical characteristics attributed to the dipeptides under study.

Dipeptide ^a	Dry-Cured Ham Parental Protein ^b	Net Charge (Value (pI)) ^c	Hydrophobicity ^d	Steric Hindrance ^d	Main Residue Attribute (N-residue, C-residue) ^c
AH	Unknown	0.1 (7.88)	−0.08	0.26	aliphatic, basic
DA	MLC1 [54]	−1 (0.69)	-0.23	0.64	acidic, aliphatic
DG	Unknown	−1 (0.68)	−0.28	0.72	acidic, aliphatic
EE	TTN [55] MLC1 [54]	−2 (0.85)	−0.62	0.68	acidic, acidic
ES	Unknown	−1 (1.01)	−0.44	0.60	acidic, polar
EV	Unknown	−1 (0.94)	−0.04	0.69	acidic, aliphatic
VG	Unknown	0 (3.59)	0.35	0.69	aliphatic, aliphatic

^a Peptide sequences are given in one-letter code. ^b Known parental protein of origin, MLC1: myosin light chain 1; TTN; titin. ^c Net charges at pH 7, pI values, and main residue attribute obtained from PepCalc (https://pepcalc.com/) (accessed on June 2020). ^d Hydrophobicity and steric hindrance values obtained from ToxinPred [56].

Table 2. Rattus norvegicus closed–open conformation (PDB ID: 1EWK) of mGluR1 residues involved in docking interactions with glutamic acid and the umami dry-cured ham dipeptides of this study, with docking scores.

Ligand	PubChem ID	Binding Energy (kcal/mol)	Inhibition Constant (µM)	Protein Residues Involved in H-Bond Interactions [Chain:Residue (Distance btw Donor-Acceptor) (Protein Donor/Acceptor, Residue from Side Chain)]	No. of H-Bonds	Protein Residues Involved in Hydrophobic Interactions[Chain:Residue (Distance btw Carbon Atoms)]	Protein Residues Involved in Salt Bridges [Chain:Residue (Distance btw Centers of Charge) (Ligand Functional Group Providing the Charge)]
E	33,032	−6.56	15.58	A:Tyr74 (2.80 Å) (Donor,sd) A:Tyr74 (2.89 Å) (Acceptor,sd) A:Ser165 (3.03 Å) (Donor) A:Ser165 (2.86 Å) (Acceptor,sd) A:Ser186 (4.08 Å) (Donor,sd) A:Thr188 (2.80 Å) (Donor) A:Asp318 (3.47 Å) (Acceptor,sd)	7	Absent	A:Arg323 (5.39 Å) (Carboxilate) A:Lys409 (3.25 Å) (Carboxilate)
AH	9,837,455	−6.93	8.26	A:Tyr74 (2.84 Å) (Donor,sd) A:Tyr74 (2.84 Å) (Acceptor,sd) A:Ser186 (2.82 Å) (Donor,sd) A:Ser186 (3.88 Å) (Acceptor,sd) A:Tyr236 (3.74 Å) (Acceptor,sd) A:Glu292 (4.02 Å) (Acceptor,sd) A:Gly293 (3.57 Å) (Donor) A:Arg323 (2.79 Å) (Donor,sd)	8	A:Trp110 (3.86 Å) A:Tyr236 (3.27 Å)	A:Arg78 (4.47 Å) (Carboxilate) A:Lys409 (3.49 Å) (Carboxilate)
DA	5,491,963	−6.23	27.24	A:Tyr74 (2.68 Å) (Donor,sd) A:Ser165 (3.12 Å) (Donor) A:Ser165 (2.73 Å) (Acceptor,sd) A:Thr188 (3.16 Å) (Donor) A:Gly293 (3.06 Å) (Donor) A:Asp318 (3.44 Å) (Acceptor,sd) A:Gly319 (3.08 Å) (Acceptor) A:Lys409 (3.69 Å) (Donor,sd)	8	A:Tyr236 (3.13 Å) A:Glu292 (3.17 Å)	A:Arg323 (4.24 Å) (Carboxilate) A:Lys409 (5.38 Å) (Carboxilate)
DG	151,148	−7.12	6.00	A:Tyr74 (3.13 Å) (Acceptor,sd) A:Gly163 (3.73 Å) (Acceptor) A:Ser165 (2.72 Å) (Donor) A:Ser165 (2.77 Å) (Acceptor,sd) A:Ser186 (2.82 Å) (Donor,sd) A:Thr188 (3.05 Å) (Donor) A:Asp318 (3.46 Å) (Acceptor,sd) A:Lys409 (3.90 Å) (Donor,sd)	8	A:Tyr236 (3.48 Å)	A:Arg78 (3.56 Å) (Carboxilate) A:Lys409 (3.97 Å) (Carboxilate)
EE	439,500	5.77	59.42	A:Tyr74 (2.97 Å) (Acceptor,sd) A:Tyr74 (3.22 Å) (Donor,sd) A:Tyr74 (3.22 Å) (Acceptor,sd) A:Ser165 (2.73 Å) (Donor) A:Ser186 (2.76 Å) (Donor,sd) A:Ser186 (2.61 Å) (Acceptor) A:Thr188 (2.99 Å) (Donor) A:Gly293 (3.41 Å) (Donor) A:Met294 (3.14 Å) (Donor) A:Gly319 (2.55 Å) (Acceptor) A:Arg323 (2.44 Å) (Donor,sd)	11	A:Tyr74 (3.33 Å) A:Trp110 (3.10 Å) A:Trp110 (3.51 Å) A:Glu292 (3.54 Å)	A:Arg71 (4.74 Å) (Carboxilate) A:Arg78 (4.28 Å) (Carboxilate) A:Arg323 (4.21 Å) (Carboxilate) A:Lys409 (3.60 Å) (Carboxilate)
ES	6,995,653	−6.87	9.17	A:Tyr74 (3.46 Å) (Donor,sd) A:Tyr74 (3.46 Å) (Acceptor,sd) A:Tyr74 (2.80 Å) (Acceptor,sd) A:Ser166 (2.97 Å) (Donor,sd) A:Gly293 (3.68 Å) (Donor) A:Met294 (3.03 Å) (Donor) A:Asp318 (3.57 Å) (Acceptor,sd) A:Arg323 (2.94 Å) (Donor,sd) A:Arg323 (3.86 Å) (Donor,sd)	9	A:Trp110 (3.12 Å) A:Lys409 (3.84 Å)	A:Arg71 (3.44 Å) (Carboxilate) A:Arg78 (3.72 Å) (Carboxilate) A:Arg323 (4.04 Å) (Carboxilate) A:Lys409 (3.99 Å) (Carboxilate)
EV	6,992,567	−6.96	7.87	A:Tyr74 (3.77 Å) (Acceptor,sd) A:Tyr74 (3.83 Å) (Donor,sd) A:Glu292 (3.65 Å) (Acceptor,sd) A:Glu292 (3.28 Å) (Acceptor,sd) A:Gly293 (2.85 Å) (Donor) A:Met294 (3.11 Å) (Donor) A:Asp318 (2.91 Å) (Acceptor,sd) A:Arg323 (2.55 Å) (Donor,sd)	8	A:Trp110 (3.48 Å) A:Glu292 (3.03 Å) A:Met294 (3.19 Å)	A:Arg71 (4.49 Å) (Carboxilate) A:Arg323 (3.19 Å) (Carboxilate) A:Lys409 (2.69 Å) (Carboxilate)
VG	6,993,111	−8.31	0.811	A:Tyr74 (2.93 Å) (Acceptor,sd) A:Gly163 (3.57 Å) (Acceptor) A:Ser186 (2.72 Å) (Donor,sd) A:Thr188 (3.47 Å) (Acceptor,sd) A:Lys409 (3.96 Å) (Donor,sd)	5	A:Tyr236 (3.44 Å) A:Tyr236 (3.37 Å)	A:Arg78 (3.66 Å) (Carboxilate) A:Lys409 (3.75 Å) (Carboxilate)

Key residues of the binding site are highlighted in bold. Common residues for which glutamate and dipeptides interact are colored in purple.

Table 3. Rattus norvegicus open–open conformation (PDB ID: 1EWT) of mGluR1 residues involved in docking interactions with glutamic acid and the umami dry-cured ham dipeptides of this study, with docking scores.

Ligand	PubChem ID	Binding Energy (kcal/mol)	Inhibition Constant (µM)	Protein Residues Involved in H-Bond Interactions [Chain:Residue (Distance btw Donor-Acceptor) (Protein Donor/Acceptor, Residue from Side Chain)]	No. of H-Bonds	Protein Residues Involved in Hydrophobic Interactions [Chain:Residue (Distance btw Carbon Atoms)]	Protein Residues Involved in Salt Bridges [Chain:Residue (Distance btw Centers of Charge) (Ligand Functional Group Providing the Charge)]
E	33,032	−4.31	694.05	A:Tyr74 (3.31 Å) (Acceptor,sd) A:Tyr74 (2.97 Å) (Acceptor,sd) A:Tyr74 (2.57 Å) (Acceptor,sd) A:Ser186 (3.00 Å) (Donor,sd)	4	A:Trp110 (3.30 Å)	A:Arg78 (3.91 Å) (Carboxilate) A:Lys409 (3.90 Å) (Carboxilate) A:Lys409 (2.49 Å) (Carboxilate)
AH	9,837,455	−6.70	12.32	A:Tyr74 (3.40 Å) (Acceptor,sd) A:Tyr74 (2.59 Å) (Acceptor,sd) A:Gly163 (2.74 Å) (Acceptor) A:Ser165 (3.43 Å) (Donor) A:Ser186 (2.99 Å) (Donor,sd) A:Thr188 (3.46 Å) (Acceptor,sd) A:Lys409 (2.93 Å) (Donor,sd)	7	A:Trp110 (3.31 Å) A:Trp110 (3.48 Å)	A:Arg78 (3.85 Å) (Carboxilate) A:Lys409 (3.91 Å) (Carboxilate)
DA	5,491,963	−4.76	322.75	A:Tyr74 (3.36 Å) (Acceptor,sd) A:Glu292 (3.65 Å) (Donor,sd) A:Glu292 (3.65 Å) (Acceptor,sd)	3	Absent	A:Arg71 (3.58 Å) (Carboxilate) A:Lys409 (2.77 Å) (Carboxilate)
DG	151,148	−4.60	424.75	A:Tyr74 (2.79 Å) (Acceptor,sd) A:Tyr74 (2.38 Å) (Acceptor,sd) A:Tyr74 (3.00 Å) (Donor,sd) A:Ser186 (3.10 Å) (Donor,sd) A:Lys409 (3.76 Å) (Acceptor,sd)	5	Absent	A:Arg78 (4.39 Å) (Carboxilate) A:Arg323 (4.91 Å) (Carboxilate) A:Lys409 (3.28 Å) (Carboxilate) A:Lys409 (3.81 Å) (Carboxilate)
EE	439,500	−6.21	27.93	A:Tyr74 (3.75 Å) (Acceptor,sd) A:Ser186 (3.02 Å) (Donor,sd) A:Glu292 (3.06 Å) (Donor,sd) A:Glu292 (3.06 Å) (Acceptor,sd)	4	A:Tyr74 (3.42 Å) A:Trp110 (3.16 Å) A:Trp110 (3.02 Å)	A:Arg71 (3.50 Å) (Carboxilate) A:Arg78 (3.65 Å) (Carboxilate) A:Lys409 (4.16 Å) (Carboxilate) A:Lys409 (3.40 Å) (Carboxilate)
ES	6,995,653	−4.17	875.75	A:Tyr74 (2.82 Å) (Acceptor,sd) A:Tyr74 (2.64 Å) (Acceptor,sd) A:Ser186 (3.76 Å) (Donor,sd) A:Asp318 (2.83 Å) (Accpetor,sd) A:Ser408 (4.07 Å) (Donor,sd) A:Lys409 (3.00 Å) (Donor,sd)	6	A:Tyr74 (3.70 Å) A:Trp110 (3.30 Å)	A:Lys409 (2.99 Å) (Carboxilate) A:Lys409 (2.88 Å) (Carboxilate)
EV	6,992,567	−6.17	29.93	A:Tyr74 (2.57 Å) (Acceptor,sd) A:Tyr74 (3.86 Å) (Acceptor,sd) A:Glu292 (2.53 Å) (Donor,sd) A:Glu292 (2.53 Å) (Acceptor,sd)	4	A:Trp110 (2.96 Å) A:Glu292 (3.64 Å)	A:Arg71 (3.44 Å) (Carboxilate) A:Lys409 (2.59 Å) (Carboxilate)
VG	6,993,111	−5.90	47.1	A:Trp110 (2.96 Å) (Donor,sd) A:Glu292 (2.57 Å) (Donor,sd) A:Glu292 (2.57 Å) (Acceptor,sd)	3	A:Tyr236 (3.83 Å) A:Glu292 (3.92 Å)	A:Arg71 (3.50 Å) (Carboxilate)

Key residues of the binding site are highlighted in bold. Common residues for which glutamate and dipeptides interact are colored in purple.

Table 4. Homo sapiens open–open conformation (PDB ID: 3KS9) of mGluR1 residues involved in docking interactions with glutamic acid and the umami dry-cured ham dipeptides of this study, with docking scores.

Ligand	PubChem ID	Binding Energy (kcal/mol)	Inhibition Constant (µM)	Protein Residues Involved in H-Bond Interactions [Chain:Residue (Distance btw Donor-Acceptor) (Protein Donor/Acceptor, Residue from Side Chain)]	No. of H Bonds	Protein Residues Involved in Hydrophobic Interactions [Chain:Residue (Distance btw Carbon Atoms)]	Protein residues involved in Salt Bridges [Chain:Residue (Distance btw Centers of Charge) (Ligand Functional Group providing the Charge)]	π-Stacking [Chain:Residue (Distance in atm) (Stacking Type)]
E	33,032	−4.58	438.58	A:Tyr74 (2.49 Å) (Acceptor,sd) A:Tyr74 (2.74 Å) (Acceptor,sd) A:Tyr74 (2.42 Å) (Acceptor,sd) A:Ser186 (3.17 Å) (Donor,sd)	4	A:Tyr74 (3.70 Å) A:Trp110 (3.28 Å)	A:Arg78 (3.60 Å) (Carboxilate) A:Lys409 (2.59 Å) (Carboxilate) A:Lys409 (4.74 Å) (Carboxilate)	Absent
AH	9,837,455	−6.83	9.93	A:Ser165 (2.96 Å) (Donor) A:Ser186 (2.88 Å) (Acceptor) A:Thr188 (3.27 Å) (Donor,sd) A:Asn235 (2.78 Å) (Acceptor,sd) A:Tyr236 (3.53 Å) (Donor) A:Thr188 (3.27 Å) (Acceptor,sd) A:Asp208 (3.73 Å) (Acceptor,sd) A:Gln211 (3.37 Å) (Donor,sd)	8	A:Thr188 (3.51 Å)	Absent	A:Tyr236 (5.31 Å) (⊥)
DA	5,491,963	−5.50	92.95	A:Ser165 (2.94 Å) (Donor) A:Ser186 (2.58 Å) (Acceptor) A:Ser186 (2.80 Å) (Acceptor) A:Thr188 (2.76 Å) (Donor) A:Thr188 (2.70 Å) (Acceptor,sd) A:Gln211 (3.44 Å) (Donor,sd) A:Asp318 (2.91 Å) (Acceptor,sd)	7	A:Thr188 (3.22 Å)	A:Lys409 (3.58 Å) (Carboxilate)	Absent
DG	151,148	−4.82	294.68	A:Ser165 (2.93 Å) (Donor) A:Ser186 (3.99 Å) (Acceptor) A:Ser186 (2.70 Å) (Acceptor) A:Ser186 (2.98 Å) (Acceptor) A:Asp208 (3.83 Å) (Acceptor,sd)	5	A:Thr188 (3.25 Å)	A:Lys409 (3.25 Å) (Carboxilate)	Absent
EE	439,500	−4.92	248.83	A:Ser165 (2.99 Å) (Donor) A:Ser186 (3.54 Å) (Donor,sd) A:Thr188 (2.68 Å) (Donor) A:Thr188 (2.87 Å) (Acceptor,sd) A:Thr188 (3.07 Å) (Acceptor,sd) A:Ser189 (3.87 Å) (Donor) A:Asp208 (3.25 Å) (Acceptor,sd) A:Asp318 (2.92 Å) (Acceptor,sd)	8	A:Thr188 (3.03 Å) A:Leu342 (3.10 Å)	A:Lys409 (3.10 Å) (Carboxilate) A:Lys409 (3.28 Å) (Carboxilate)	Absent
ES	6,995,653	−5.16	165.54	A:Ser165 (2.91 Å) (Donor) A:Thr188 (2.78 Å) (Acceptor,sd) A:Thr188 (2.79 Å) (Donor) A:Thr188 (2.67 Å) (Acceptor,sd) A:Thr188 (2.89 Å) (Acceptor,sd) A:Ser189 (4.07 Å) (Donor) A:Gln211 (3.73 Å) (Donor,sd) A:Asp318 (3.88 Å) (Acceptor,sd)	8	A:Thr188 (3.40 Å) A:Leu342 (3.51 Å)	A:Lys409 (2.55 Å) (Carboxilate)	Absent
EV	6,992,567	−6.11	33.23	A:Ser165 (3.02 Å) (Donor) A:Ser186 (2.89 Å) (Acceptor) A:Thr188 (2.62 Å) (Donor) A:Thr188 (2.68 Å) (Acceptor,sd) A:Thr188 (3.01 Å) (Acceptor,sd) A:Ser189 (3.86 Å) (Donor) A:Gln211 (3.87 Å) (Donor,sd) A:Asp318 (3.13 Å) (Acceptor,sd)	8	A:Thr188 (2.97 Å) A:Leu342 (3.52 Å)	A:Lys409 (3.04 Å) (Carboxilate)	Absent
VG	6,993,111	−6.49	17.44	A:Ser165 (3.02 Å) (Donor) A:Thr188 (2.80 Å) (Donor) A:Thr188 (2.83 Å) (Acceptor,sd) A:Thr188 (2.65 Å) (Acceptor,sd) A:Gln211 (3.24 Å) (Donor,sd) A:Asp318 (2.86 Å) (Acceptor,sd)	6	A:Thr188 (3.28 Å) A:Leu342 (3.67 Å)	Absent	Absent

Key residues of the binding site are highlighted in bold. Common residues for which glutamate and dipeptides interact are colored in purple.

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Heres, A.; Toldrá, F.; Mora, L. Characterization of Umami Dry-Cured Ham-Derived Dipeptide Interaction with Metabotropic Glutamate Receptor (mGluR) by Molecular Docking Simulation. Appl. Sci. 2021, 11, 8268. https://doi.org/10.3390/app11178268

AMA Style

Heres A, Toldrá F, Mora L. Characterization of Umami Dry-Cured Ham-Derived Dipeptide Interaction with Metabotropic Glutamate Receptor (mGluR) by Molecular Docking Simulation. Applied Sciences. 2021; 11(17):8268. https://doi.org/10.3390/app11178268

Chicago/Turabian Style

Heres, Alejandro, Fidel Toldrá, and Leticia Mora. 2021. "Characterization of Umami Dry-Cured Ham-Derived Dipeptide Interaction with Metabotropic Glutamate Receptor (mGluR) by Molecular Docking Simulation" Applied Sciences 11, no. 17: 8268. https://doi.org/10.3390/app11178268

APA Style

Heres, A., Toldrá, F., & Mora, L. (2021). Characterization of Umami Dry-Cured Ham-Derived Dipeptide Interaction with Metabotropic Glutamate Receptor (mGluR) by Molecular Docking Simulation. Applied Sciences, 11(17), 8268. https://doi.org/10.3390/app11178268

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Characterization of Umami Dry-Cured Ham-Derived Dipeptide Interaction with Metabotropic Glutamate Receptor (mGluR) by Molecular Docking Simulation

Abstract

1. Introduction

2. Materials and Methods

3. Results and Discussion

3.1. Rattus Norvegicus and Homo sapiens mGluR1s Shared Homology

3.2. Interaction between Umami Dipeptides and Rattus Norvegicus mGluR1 Closed–Open Conformation

3.3. Interaction between Umami Dipeptides and Rattus Norvegicus mGluR1 Open–Open Conformation

3.4. Interaction between Umami Dipeptides and Homo sapiens mGluR1 Open–Open Conformation

4. Conclusions

Author Contributions

Funding

Institutional Review Board Statement

Informed Consent Statement

Data Availability Statement

Acknowledgments

Conflicts of Interest

References

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