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Cell-mediated Immune Responses01:40

Cell-mediated Immune Responses

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Related Experiment Video

Updated: Jun 27, 2026

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
07:59

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes

Published on: March 25, 2014

COBEpro: a novel system for predicting continuous B-cell epitopes.

Michael J Sweredoski1, Pierre Baldi

  • 1Department of Computer Science, University of California, Irvine, 92697-3435, USA.

Protein Engineering, Design & Selection : PEDS
|December 17, 2008
PubMed
Summary
This summary is machine-generated.

Predicting continuous B-cell epitopes is challenging. COBEpro, a novel system, improves prediction accuracy for continuous B-cell epitopes using a two-step approach and machine learning.

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Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
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Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope

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Last Updated: Jun 27, 2026

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
07:59

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes

Published on: March 25, 2014

Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
08:09

Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope

Published on: March 24, 2017

Area of Science:

  • Computational immunology
  • Bioinformatics
  • Vaccine development

Background:

  • Accurate prediction of B-cell epitopes is crucial but challenging.
  • Continuous B-cell epitopes are important for peptide vaccines and therapeutic proteins.
  • Existing predictors often focus on continuous epitopes due to simpler requirements.

Purpose of the Study:

  • To present COBEpro, a novel two-step system for predicting continuous B-cell epitopes.
  • To enable epitopic propensity scoring for peptide fragments and individual residues.
  • To improve the accuracy of B-cell epitope prediction.

Main Methods:

  • COBEpro utilizes a two-step prediction system.
  • A support vector machine predicts epitopic propensity on short peptide fragments.
  • Residue-level propensity scores are calculated based on fragment predictions, with optional incorporation of secondary structure and solvent accessibility information.

Main Results:

  • COBEpro achieved a cross-validated AUC of 0.829 for fragment epitopic propensity scoring.
  • The system reached an AUC of 0.628 for residue epitopic propensity scoring.
  • Performance can be enhanced by including secondary structure and solvent accessibility data.

Conclusions:

  • COBEpro offers a novel and effective approach for predicting continuous B-cell epitopes.
  • The system provides valuable propensity scores for both fragments and residues.
  • COBEpro is integrated into the SCRATCH prediction suite for broader accessibility.