Crystal structure of a TAPBPR-MHC I complex reveals the mechanism of peptide editing in antigen presentation

Science. 2017 Nov 24;358(6366):1064-1068. doi: 10.1126/science.aao5154. Epub 2017 Oct 12.

Abstract

Central to CD8+ T cell-mediated immunity is the recognition of peptide-major histocompatibility complex class I (p-MHC I) proteins displayed by antigen-presenting cells. Chaperone-mediated loading of high-affinity peptides onto MHC I is a key step in the MHC I antigen presentation pathway. However, the structure of MHC I with a chaperone that facilitates peptide loading has not been determined. We report the crystal structure of MHC I in complex with the peptide editor TAPBPR (TAP-binding protein-related), a tapasin homolog. TAPBPR remodels the peptide-binding groove of MHC I, resulting in the release of low-affinity peptide. Changes include groove relaxation, modifications of key binding pockets, and domain adjustments. This structure captures a peptide-receptive state of MHC I and provides insights into the mechanism of peptide editing by TAPBPR and, by analogy, tapasin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antigen Presentation*
  • Crystallography, X-Ray
  • Histocompatibility Antigens Class I / chemistry*
  • Histocompatibility Antigens Class I / ultrastructure
  • Humans
  • Immunoglobulins / chemistry*
  • Immunoglobulins / ultrastructure
  • Membrane Proteins / chemistry*
  • Membrane Proteins / ultrastructure
  • Peptides / chemistry
  • Protein Conformation
  • Surface Plasmon Resonance
  • beta 2-Microglobulin / chemistry*
  • beta 2-Microglobulin / ultrastructure

Substances

  • Histocompatibility Antigens Class I
  • Immunoglobulins
  • Membrane Proteins
  • Peptides
  • TAPBPL protein, human
  • beta 2-Microglobulin