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10.1186/s12967-016-0928-3

http://scihub22266oqcxt.onion/10.1186/s12967-016-0928-3
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C4908730!4908730!27301453
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suck abstract from ncbi


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pmid27301453      J+Transl+Med 2016 ; 14 (ä): ä
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  • ProInflam: a webserver for the prediction of proinflammatory antigenicity of peptides and proteins #MMPMID27301453
  • Gupta S; Madhu MK; Sharma AK; Sharma VK
  • J Transl Med 2016[]; 14 (ä): ä PMID27301453show ga
  • Background: Proinflammatory immune response involves a complex series of molecular events leading to inflammatory reaction at a site, which enables host to combat plurality of infectious agents. It can be initiated by specific stimuli such as viral, bacterial, parasitic or allergenic antigens, or by non-specific stimuli such as LPS. On counter with such antigens, the complex interaction of antigen presenting cells, T cells and inflammatory mediators like IL1?, IL1?, TNF?, IL12, IL18 and IL23 lead to proinflammatory immune response and further clearance of infection. In this study, we have tried to establish a relation between amino acid sequence of antigen and induction of proinflammatory response. Results: A total of 729 experimentally-validated proinflammatory and 171 non-proinflammatory epitopes were obtained from IEDB database. The A, F, I, L and V amino acids and AF, FA, FF, PF, IV, IN dipeptides were observed as preferred residues in proinflammatory epitopes. Using the compositional and motif-based features of proinflammatory and non-proinflammatory epitopes, we have developed machine learning-based models for prediction of proinflammatory response of peptides. The hybrid of motifs and dipeptide-based features displayed best performance with MCC = 0.58 and an accuracy of 87.6 %. Conclusion: The amino acid sequence-based features of peptides were used to develop a machine learning-based prediction tool for the prediction of proinflammatory epitopes. This is a unique tool for the computational identification of proinflammatory peptide antigen/candidates and provides leads for experimental validations. The prediction model and tools for epitope mapping and similarity search are provided as a comprehensive web server which is freely available at http://metagenomics.iiserb.ac.in/proinflam/ and http://metabiosys.iiserb.ac.in/proinflam/. Electronic supplementary material: The online version of this article (doi:10.1186/s12967-016-0928-3) contains supplementary material, which is available to authorized users.
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