Identification of B Cell and T Cell Epitopes Using Synthetic Peptide Combinatorial Libraries

Curr Protoc. 2022 Mar;2(3):e378. doi: 10.1002/cpz1.378.

Abstract

This article presents a combinatorial library method that consists of the synthesis and screening of mixture-based synthetic combinatorial libraries of peptide molecules to identify B and T cell epitopes. The protocols employ peptide libraries to identify peptides recognized by MAbs and T cells. The first protocol uses a positional scanning peptide library made up of hexapeptides to identify antigenic determinants recognized by MAbs. The 120 mixtures in the hexapeptide library are tested for their inhibitory activity in a competitive ELISA. The second protocol uses a decapeptide library to identify T cell peptide ligands. The 200 mixtures of the decapeptide library are tested for their ability to induce T cell activation. Support protocols cover optimization of the assay conditions for each MAb or T cell, to achieve the best level of sensitivity and reproducibility, and preparation of a hexapeptide library, along with deconvolution approaches. © 2022 Wiley Periodicals LLC. Basic Protocol 1: Screening peptide library for antibody inhibition Basic Protocol 2: Screening a peptide library to identify CD4+ Or CD8+ T cell ligands Support Protocol 1: Optimizing antigen and antibody concentrations for screening assay Support Protocol 2: Preparing a positional scanning peptide library.

Keywords: B cell; B cell epitopes; T cell; T cell epitopes; antigen discovery; epitopes; peptide ligands.

MeSH terms

  • B-Lymphocytes
  • Epitopes, T-Lymphocyte*
  • Peptide Library*
  • Peptides
  • Reproducibility of Results

Substances

  • Epitopes, T-Lymphocyte
  • Peptide Library
  • Peptides