DeepBCE: Evaluation of deep learning models for identification of immunogenic B-cell epitopes.

Journal: Computational biology and chemistry
PMID:

Abstract

B-Cell epitopes (BCEs) can identify and bind with receptor proteins (antigens) to initiate an immune response against pathogens. Understanding antigen-antibody binding interactions has many applications in biotechnology and biomedicine, including designing antibodies, therapeutics, and vaccines. Lab-based experimental identification of these proteins is time-consuming and challenging. Computational techniques have been proposed to discover BCEs, but most lack of significant accomplishments. This work uses classical and deep learning models (DLMs) with sequence-based features to predict immunity stimulator BCEs from proteomics sequences. The proposed convolutional neural network-based model outperforms other models with an accuracy (ACC) of 0.878, an F-measure of 0.871, and an area under the receiver operating characteristic curve (AUC) of 0.945. The proposed strategy achieves 58.7% better results on average than other state-of-the-art approaches based on the Mathews Correlation Coefficient (MCC) results. The established model is accessible through a web application located at http://deeplbcepred.pythonanywhere.com.

Authors

  • Muhammad Attique
    Department of Software, Sejong University, Seoul 05006, Korea.
  • Tamim Alkhalifah
    Department of Computer, College of Science and Arts in Ar Rass, Qassim University, Buraydah 52571, Saudi Arabia.
  • Fahad Alturise
    Department of Computer, College of Science and Arts in Ar Rass, Qassim University, Ar Rass 58892, Qassim, Saudi Arabia.
  • Yaser Daanial Khan
    Department of Computer Science, School of Systems and Technology, University of Management and Technology, P.O. Box 10033, C-II, Johar Town, Lahore 54770, Pakistan.