Prediction of TAP Transport of Peptides with Variable Length Using TAPREG

Methods Mol Biol. 2023:2673:227-235. doi: 10.1007/978-1-0716-3239-0_16.

Abstract

CD8 T cells recognize short peptides, more frequently of nine residues, presented by class I major histocompatibility complex (MHC I) molecules in the cell surface of antigen-presenting cells. These epitope peptides are loaded onto MHC I molecules in the endoplasmic reticulum, where they are shuttled from the cytosol by the transporter associated with antigen processing (TAP) as such or as N-terminal extended precursors of up to 16 residues. In this chapter, we describe the use of TAPREG, a tool for predicting TAP binding affinity that has been enhanced to identify potential CD8 T cell epitope precursors transported by TAP. TAPREG is available for free public use at http://imed.med.ucm.es/Tools/tapreg/ .

Keywords: Epitope prediction; Peptide transport; TAP; TAPREG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters* / metabolism
  • Antigen Presentation
  • Histocompatibility Antigens Class I / metabolism
  • Membrane Transport Proteins
  • Peptides* / chemistry

Substances

  • ATP-Binding Cassette Transporters
  • Peptides
  • Membrane Transport Proteins
  • Histocompatibility Antigens Class I