Prediction of anti-inflammatory proteins/peptides: an insilico approach
- Sudheer Gupta†1,
- Ashok K. Sharma†1,
- Vibhuti Shastri1,
- Midhun K. Madhu1 and
- Vineet K. Sharma1Email author
© The Author(s) 2017
Received: 13 August 2016
Accepted: 1 December 2016
Published: 6 January 2017
The current therapy for inflammatory and autoimmune disorders involves the use of nonspecific anti-inflammatory drugs and other immunosuppressant, which are often accompanied with potential side effects. As an alternative therapy, anti-inflammatory peptides are recently being exploited as anti-inflammatory agents for treatment of various inflammatory diseases such as Alzheimer’s disease and rheumatoid arthritis. Thus, understanding the correlation between amino acid sequence and its potential anti-inflammatory property is of great importance for the discovery of novel and efficient anti-inflammatory peptide-based therapeutics.
In this study, we have developed a prediction tool for the classification of peptides as anti-inflammatory epitopes or non anti-inflammatory epitopes. The training was performed using experimentally validated epitopes obtained from Immune epitope database and analysis resource database. Different sequence-based features and their hybrids with motif information were employed for development of support vector machine-based machine learning models. Similarly, machine learning models were also constructed using random forest.
The composition and terminal residue conservation analysis of peptides revealed the dominance of leucine, serine, tyrosine and arginine residues in anti-inflammatory epitopes as compared to non anti-inflammatory epitopes. Similarly, the anti-inflammatory epitopes specific motifs were found to be rich in hydrophobic and polar residues. The hybrid of tripeptide composition-based support vector machine model and motif yielded the best performance on 10-fold cross validation with an accuracy of 78.1% and MCC of 0.58. The same displayed an accuracy of 72% and MCC of 0.45 on validation dataset, rejecting any possibility of over-fitting. The tripeptide composition-based random forest model displayed an accuracy of 0.8 and MCC of 0.59 on 10-fold cross validation, however, the accuracy (0.68) and MCC (0.31) was lower as compared to support vector machine model on validation dataset. Thus, the support vector machine model is implemented as the default model and an additional option of using the random forest model is provided.
The prediction models along with tools for epitope mapping and similarity search have been provided as a web server which is freely accessible at http://metagenomics.iiserb.ac.in/antiinflam/.
For maintenance of immune homeostasis and restricting the occurrence of aggravated inflammation and autoimmunity, the induction of immune tolerance is crucial . The effect of multiple mechanisms working in concert is necessary for the upkeep of the state of tolerance. Several endogenous peptides identified during inflammatory responses have emerged as anti-inflammatory agents that can be employed in new therapies for inflammatory and autoimmune conditions . The immunotherapeutic ability of these anti-inflammatory peptides in the inhibition of antigen-specific T(H)1-driven responses, and in the generation of regulatory T cells has numerous clinical applications .
Several synthetic and natural peptides are known to inhibit the signal transduction pathways for expression of inflammatory cytokines. For example, intranasal treatment of amyloid-beta (Abeta) peptide in mice with neuropathological symptoms of Alzheimer’s disease showed a decreased A-beta plaque burden along with anti-inflammatory cytokines IL-4, IL-10 and tumor growth factor-beta . Another neuropeptide: vasoactive intestinal peptide (VIP) is also known to reduce the inflammatory and autoimmune components of rheumatoid arthritis in the experimental model . Similarly, there are pieces of evidence showing production of pro-inflammatory cytokines and microglial activation during age-related cognitive deficits in the hippocampal region. A mimetic peptide FG Loop(FGL) derived from the neural cell adhesion molecule (NCAM) is shown to work as a novel anti-inflammatory agent in such age-related disorders . Furthermore, nonapeptides, Anti inflammin 1 and 2, can potentially reduce leukocyte trafficking in host defense and inflammation by inhibiting PMN adhesion to HCAEC by attenuating up-regulation of CD11/CD18 expression on leukocytes . Moreover, certain synthetic peptides are known to be involved in inhibition of early signal transduction pathways of inflammatory cytokines. One notable example is the role of intravesical RDP58 in interstitial cystitis (IC) inflammation-induced neurotrophic changes in the bladder. Mice models treated with RDP58 shows near complete abolition of LPS induced production of TNF-α in the bladder .
Taken together, the availability of experimental data allows for the computational correlation between amino acid sequences and their anti-inflammatory properties. To the best of the authors’ knowledge, there has been no study that investigates the sequence based signature for the anti-inflammatory behavior of target peptide sequences. Understanding the association between specific amino acid sequences and the anti-inflammatory properties conferred by them is likely to facilitate their application for therapeutic purposes. One such example is of altered peptide ligands (APLs) and their role in therapeutic modulation of T cell function . The aim of this study was to examine the amino acid sequences of experimentally validated anti-inflammatory epitopes (AIEs) and non anti-inflammatory epitopes (NAIEs) and develop a machine learning based classification method that incorporates the sequence based features to predict the anti-inflammatory nature of various peptides and proteins.
Preparation of dataset
Input features for machine learning
Amino acid composition
Identification of functional motifs in amino acid sequences is one of the widely used techniques in the functional annotation of peptides/proteins. Several previous immunoinformatics studies have examined the immunologically relevant motifs in peptides for various purposes [17–19]. To identify the motifs specific to AIEs by comparing it with NAIEs, MERCI software was used . The identification of motifs in positive data by comparing with negative data yields motifs exclusive for the positive data. Motifs specific for NAIEs were also identified by MERCI software in a similar manner. The maximum length of the motif was set to 9 amino acids because the core size of both MHC I and II equals nine amino acids [21, 22]. The gap length was set to the default length of 1.
Hybrid models of AAC, DPC, and TPC with MERCI-based motifs were also constructed in this study [23, 24]. The presence of anti-inflammatory and non anti-inflammatory specific motifs in every peptide in the training dataset was examined. If the epitope contained the anti-inflammatory motifs, a weightage of +1 was added to its AAC, DPC or TPC based SVM score. Similarly, if the epitope is positive for non anti-inflammatory motifs, the weight was added as −1 for the same.
Machine-learning-based prediction models
Caret package in R was used to evaluate the performance of various machine learning methods such as support vector machine (SVM), Random Forest (RF), k-nearest neighbors (kNN), linear discriminant analysis (LDA) and classification and regression tree (CART). Based on the results, SVM and RF were used as the machine learning algorithms for building predictive models through SVMlight package available at http://svmlight.joachims.org/ and randomForest package available at https://cran.r-project.org/web/packages/randomForest/index.html. Machine learning algorithms have also been used in previous studies for developing tools for immune epitope prediction with good performances [15, 25–28].
Performance evaluation of models
The comparison of different machine learning methods to select the best method is essential in predictive modelling. A 10-fold cross-validation technique was employed for different learning methods and evaluated on a separate unseen validation dataset. To carry out the 10-fold cross-validation, the data was divided into ten parts of which nine parts were used for training and the tenth segment was used for testing. The procedure is repeated ten times to test the learning methods on each part. The result of all ten predictions was taken together for evaluating the performance of various models built by different methods. For measuring the performance of each model, threshold dependent and threshold independent parameters were used. For all models, area under curve (AUC), a threshold independent parameter was calculated using PERF . Threshold-dependent parameters such as sensitivity (Sen), specificity (Spec), accuracy (Acc) and Matthews’s correlation coefficient (MCC) were also calculated for all models. The following equations were used for calculating the threshold dependent parameters.
(TN = true negative, FP = false positive, TP = true positive, FN = false negative; Sens = sensitivity; Spec = specificity; Acc = accuracy)
Similarly, the TPC analysis also revealed several tripeptides which were highly abundant in AIEs as compared to NAIEs. A total of 122 tripeptides were found significantly abundant (p value ≤0.01, Welch’s t-test) in AIEs (Additional file 1: Table S1). In particular, Ser–Leu–Ser (SLS), Leu–Lys–Leu (LKL), Leu–Arg–Leu (LRL) etc. are highly abundant in AIEs and their constituent dipeptides and amino acids are also abundant in AAC and DPC analysis.
HLA allele distribution
Annotation and coverage of MERCI motifs extracted from anti-inflammatory epitopes
Hydrophobic hydrophobic tiny F charged
Hydrophobic L hydrophobic hydrophobic small polar hydrophobic polar polar
Hydrophobic I hydrophobic hydrophobic hydrophobic hydrophobic hydrophobic polar polar
Polar L aliphatic hydrophobic positive
Hydrophobic aliphatic hydrophobic aliphatic small polar hydrophobic polar polar
Hydrophobic hydrophobic small hydrophobic polar hydrophobic polar Q
L hydrophobic aliphatic small polar hydrophobic polar polar
Hydrophobic polar hydrophobic L polar hydrophobic hydrophobic polar tiny
Hydrophobic L polar polar small small hydrophobic hydrophobic
Hydrophobic aliphatic polar small hydrophobic charged polar polar hydrophobic
Hydrophobic hydrophobic hydrophobic tiny F charged
Hydrophobic hydrophobic tiny F charged hydrophobic
small aliphatic E N
Machine learning-based classification
It is apparent from the earlier analysis that AIEs and NAIEs differ in several composition-based features. Therefore, these differences can be exploited for the classification of epitopes. Machine learning-based classification was implemented to exploit the sequence-specific features for the classification and prediction of AIEs and NAIEs.
Comparison of machine learning methods
Different machine learning algorithms such as SVM, RF, kNN, LDA and CART were implemented using caret package in R for comparing their performances on the same data. Performances of SVM and RF were found better as compared to other machine learning techniques, and hence, these two machine learning methods were optimized further using amino acid, dipeptide and tripeptide composition as input features (Additional file 1: Text S1, Additional file 2: Figure S1, Additional file 3: Figure S2, Additional file 4: Figure S3, Additional file 5: Figure S4, Additional file 6: Figure S5, Additional file 7: Figure S6, Additional file 8: Figure S7, Additional file 9: Figure S8, Additional file 10: Figure S9, Additional file 11: Figure S10 and Additional file 12: Figure S11).
Performance of SVM models
Amino acid composition-based models
Dipeptide composition-based models
Dipeptide composition was also used for building the predictive machine learning model using 400 sized vectors representing all possible dipeptides. SVM model with gamma parameter (g) = 0.005, trade-off factor (c) = 1 and cost factor (j) = 3 was the best performing model with an accuracy of 70.98, MCC of 0.44 and an area under curve (AUC) of 0.79 (Fig. 6).
Tripeptide composition-based models
The local order in the form of DPC as feature yielded better predictive ability of SVM model as compared to the results obtained using AAC. However, to further evaluate the effect of local order in the form of tripeptide, TPC as input feature was used to build the SVM model. The best model performed with an accuracy of 75.04%, MCC of 0.51 and AUC of 0.81 on gamma parameter (g) = 0.001, trade-off factor (c) = 4 and cost factor (j) = 1 (Fig. 6).
Performance of RF models
Performance of SVM models using various sequence based features
g:0.005 c:1 j:4
g:0.005 c:1 j:1
g:0.001 c:2 j:1
Performance of optimized prediction models on validation dataset
TPC-based SVM model yielded the best accuracy among the three composition-based models. However, to further improve the efficiency of models, hybrid models were constructed for AAC, DPC, and TPC based models by combining each one with the motif features. The hybrid of AAC-based model (AAC_HYB) with motif features performed with 71.1% accuracy, whereas, the hybrid of DPC-based model (DPC_HYB) with motif features showed an accuracy of 74.34%. The hybrid of TPC-based model with motif features (TPC_HYB) was the best performing among all hybrid models. It showed the highest accuracy of 78.1%, MCC of 0.58 and an area under curve (AUC) of 0.86 (Fig. 6).
Performance on validation dataset
The performance of all models was evaluated on the validation data (Table 3 and Fig. 6). This evaluation was carried out in addition to cross-validation to ensure that the obtained results were not due to over-optimization. TPC_HYB model which showed the highest accuracy in 10-fold cross validation also performed well on the validation dataset (72%). These results attest that the observed results were not due to over-optimization of data.
Furthermore, all the inputs such as amino acid, dipeptides, tripeptides etc., were processed for feature selection for composition and hybrid models by CfsSubsetEval algorithm of WEKA package. This feature selection is generally carried out to reduce the input data size without compromising on the performance. The final number of input features and performances of model with reduced input features are mentioned in Additional file 1: Table S6. It is apparent from Additional file 1: Table S7 that the performances of all models were reduced on validation dataset, with the reduction of feature vector size, however, in case of TPC_HYB model, the performance showed a marginal decline on the validation dataset, and thus, this model with reduced features was integrated in the webserver for efficient analysis.
In addition to 10-fold cross validation, models were also subjected to a fivefold cross validation analysis. The performance of models using fivefold cross validation also showed similar results. The TPC_HYB model displayed the maximum accuracy of 76% and also performed better than the other models for sensitivity and specificity values. It showed an MCC value of 0.56 and an AUC measure of 0.85 (Additional file 1: Table S8). Resultantly, the TPC_HYB model was incorporated in the webserver for epitope prediction.
Balanced dataset which contained 690 samples from both positive and negative dataset was also used to examine the performance of SVM models. The TPC_HYB model displayed the maximum accuracy of 77.8% and MCC value of 0.56. The sensitivity and specificity of this model was also higher than other models (Additional file 1: Table S9).
Web server and tools
A webserver was constructed for hosting a number of tools developed in this study for predicting the anti-inflammatory nature of peptide/protein antigens. These tools employ the validated best performing model developed in the study. The web server also incorporates several other analysis tools as described below.
This module is developed for predicting the anti-inflammatory nature of small length peptides. The user can submit a single peptide or a batch of peptides with lengths ranging from 4 to 30 amino acids. A threshold option is also provided which can be tuned to increase the stringency of positive prediction. Queries are passed through anti-inflammatory epitope prediction pipeline and the results are displayed as a table which shows the prediction of a peptide as anti-inflammatory or non anti-inflammatory based on SVM or RF scores.
Every peptide sequence in the results table is provided with option for its virtual screening and design which is an additional feature that screens the variants of the peptides for anti-inflammatory property. Variants are created by substituting each amino acid position by all the 19 other naturally occurring amino acids. This option enables the user to check the anti-inflammatory nature of peptides that are similar to the query peptides.
To determine the antigenic regions in a full-length protein which can induce anti-inflammatory responses, this module has been designed to allow the submission of query proteins with longer lengths. This tool divides the protein sequences into smaller peptides and runs through the same prediction pipeline. The user can also select the desired window length of peptides for prediction. Virtual screening option is also provided similar to the peptide prediction module.
In addition to the above tools, the user may wish to map the experimentally validated anti-inflammatory antigenic regions on a query protein. This module map experimentally validated AIEs from IEDB database on the protein query sequence. The results are displayed as an alignment with links to the related assay provided by IEDB database.
Unlike the epitope mapping tool, this module identifies the similar regions in the query peptide/protein and experimentally validated AIEs. Smith–Watermann search of query sequence in IEDB database is carried for displaying the top hits. Results are shown as alignments with links to related assay in IEDB database.
Anti-inflammatory drugs have widespread applications in the field of therapeutics because of their role in the reduction of swelling and inflammation. The novel peptides with anti-inflammatory properties may also be used as therapeutic agents against several diseases such as Alzheimer’s, rheumatoid arthritis as well as gut infections. Inflammatory response at the site of infection is caused due to the production of prostaglandin, thromboxane, etc. along with a release of histamine and kinin. Though it has been shown that nature of activating signal, timing, and sequence of cytokine action as well as experimental models affect their pro- or anti-inflammatory properties, IL4, IL-10, IL-13, IFN-alpha and transforming growth factor-beta are widely recognized as anti-inflammatory cytokines . Studies have shown that anti-inflammatory drugs function by down-regulating the expressions of 5-LOX, COX-2, MMPs and NF-κB . These drugs show low efficacy in curing the inflammation and leads to hypersensitivity reactions and deterioration of the immune system . Due to the limitation of small molecule drugs, peptide-based drugs appear as better candidates in curing inflammation . Thus, developing an in silico method for predicting the anti-inflammatory properties of newly synthesized or recently discovered amino acid sequence (peptide) is very valuable.
For the identification of anti-inflammatory targets, positive (anti-inflammatory) and negative (non anti-inflammatory) samples data was curated from immune epitope database which is a well-known reference database and contain the experimentally validated data. Using a good input quality data is a key for the application of machine learning techniques.
Compositional analysis revealed the presence of selected amino acids in abundance in AIEs, which is supported by other independent studies. For example, an amino acid stretch of 8-16 of SV-IV, which is rich in Ser and Gln residues, has been reported to exhibit anti-inflammatory properties . Motif based analysis helped to determine the patterns in binding sites of target peptides on MHC molecules. Annotation of MERCI motifs from unique AIEs revealed that ‘hydrophobic hydrophobic tiny F charged’ had the maximum coverage. From this study, it was also observed that certain HLA alleles such as HLA-DRB1*04:01 alleles were more frequent in anti-inflammatory positive assays. Interestingly, the HLA-DRB1*04:01 allele has been associated with an increased occurrence of rheumatoid arthritis in the Caucasian population .
Furthermore, three different types of compositional analysis including amino acid, dipeptide and tripeptide composition were carried out to obtain the information of signature sequences, of which TPC_HYB (tripeptide hybrid with motifs derived weightage) was selected and included as the final model for webserver as a default prediction model. TPC (tripeptide composition) based RF model was also included at the webserver as an additional prediction model. The availability of two machine learning models provides flexibility and options to the users to predict epitopes using two different methods.
The inherent ability of anti-inflammatory molecules to induce anti-inflammatory cytokines has the potential to play a major role in immunology and peptide therapeutic applications. Hence, an attempt has been made to identify sequence-based signatures of anti-inflammatory peptides and a machine learning tool has been developed for the prediction of anti-inflammatory epitopes. The observed accuracy values attest the performance of the tool and to our knowledge, it is the only available tool for the prediction of anti-inflammatory epitopes. Thus, the identification of anti-inflammatory target peptide sequences using this computational server provides valuable leads for experimental validations for the scientific community. The developed computational tools for investigation of anti-inflammatory sites have been made freely available for academic usage as a web server.
amino acid composition
area under curve
immune epitope database
human leukocyte antigen
Matthews correlation coefficient
major histocompatibility factor
non anti-inflammatory epitopes
support vector machine
two sample logo
linear discriminant analysis
classification and regression tree
SG developed SVM-based models. AKS developed RF models. SG and AKS developed web server. MKM, VS, SG, AKS & VKS analysed the data and drafted the manuscript. SG and VKS conceived the work, participated in the design of the study. All authors read and approved the final manuscript.
This work was supported by the intramural funding received from IISER Bhopal. We thank MHRD, Govt of India, funded Centre for Research on Environment and Sustainable Technologies (CREST) at IISER Bhopal for its support. However, the views expressed in this manuscript are that of the authors alone and no approval of the same, explicit or implicit, by MHRD should be assumed.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used for this study are provided at http://metagenomics.iiserb.ac.in/antiinflam/data.php.
This work was supported by the intramural funding received from IISER Bhopal.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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