e-learning

Neoantigen 7: IEDB binding PepQuery Validated Neopeptides

Abstract

Neoantigens are peptides derived from tumor-specific mutations, which are recognized by the immune system as foreign and can stimulate an immune response against cancer cells. Identifying these neoantigens is a crucial step in the development of personalized cancer immunotherapies, as they serve as targets for T-cell mediated immune responses. However, predicting which peptides from the tumor genome will bind effectively to major histocompatibility complex (MHC) molecules—key proteins that present antigens to immune cells—remains a significant challenge.

About This Material

This is a Hands-on Tutorial from the GTN which is usable either for individual self-study, or as a teaching material in a classroom.

Questions this will address

  • What are neoantigens, and why are they significant in cancer immunotherapy?
  • How can binding predictions and validation help distinguish strong and weak binders?
  • What tools and techniques are commonly used for neoantigen identification and validation?

Learning Objectives

  • Understand the process of neoantigen identification and the role of peptide binding predictions.
  • Learn how to use IEDB to predict the binding affinity of peptides to MHC molecules.
  • Gain practical experience using PepQuery to validate novel peptides from proteomics data.
  • Distinguish between strong and weak binders based on predicted binding affinity.

Licence: Creative Commons Attribution 4.0 International

Keywords: Proteomics, label-free

Target audience: Students

Resource type: e-learning

Version: 1

Status: Active

Prerequisites:

  • Introduction to Galaxy Analyses
  • Proteomics

Learning objectives:

  • Understand the process of neoantigen identification and the role of peptide binding predictions.
  • Learn how to use IEDB to predict the binding affinity of peptides to MHC molecules.
  • Gain practical experience using PepQuery to validate novel peptides from proteomics data.
  • Distinguish between strong and weak binders based on predicted binding affinity.

Date modified: 2025-01-14

Date published: 2025-01-14

Authors: James Johnson, Katherine Do, Subina Mehta

Contributors: Pratik Jagtap, Timothy J. Griffin

Scientific topics: Proteomics


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