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The quantitative prediction of HLA-B*2705 peptide binding affinities using Support Vector Regression to gain insights into its role for the Spondyloarthropathies. | LitMetric

AI Article Synopsis

  • Computational methods play a crucial role in immunoinformatics, particularly for predicting peptide binding affinities, which can aid in drug design, including vaccines and disease diagnostics.
  • The study focuses on the human MHC allele HLA-B*2705, linked to spondyloarthropathies, and utilizes Support Vector Regression (SVR) to analyze the binding affinity of 222 peptides.
  • The results indicate a significant correlation coefficient of 0.65, demonstrating that SVR models are effective tools for predicting binding affinities of newly identified peptides.

Article Abstract

Computational methods are increasingly utilised in many immunoinformatics problems such as the prediction of binding affinity of peptides. The peptides could provide valuable insight into the drug design and development such as vaccines. Moreover, they can be used to diagnose diseases. The presence of human class I MHC allele HLA-B*2705 is one of the strong hypothesis that would lead spondyloarthropathies. In this paper, Support Vector Regression is used in order to predict binding affinity of peptides with the aid of experimentally determined peptide-MHC binding affinities of 222 peptides to HLA-B*2705 to get more insight into this problematic disease. The results yield a high correlation coefficient as much as 0.65 and the SVR-based predictive models can be considered as a useful tool in order to predict the binding affinities for newly discovered peptides.

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Source
http://dx.doi.org/10.1109/EMBC.2015.7320164DOI Listing

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