A role for the P1 anchor residue in the thermal stability of MHC class II molecule I-Ab

Immunol Lett. 2003 Jan 2;85(1):47-52. doi: 10.1016/s0165-2478(02)00206-7.

Abstract

The thermal stability of the murine MHC class II molecule, I-A(b), in complex with invariant chain-derived peptide (CLIP) and an antigenic peptide derived from the alpha subunit of the I-E molecule (Ealpha) at mildly acidic and neutral pH were analyzed using circular dichroism (CD). The stability of I-A(b)-CLIP was increased by a single amino acid substitution in the P1 anchor residue, from Met of CLIP to Phe of Ealpha, similar, in this respect, to I-A(b)-Ealpha. This indicates that hydrophobic interaction in the P1 pocket is critical and plays a primary role in the stability of the complex. The structural models of I-A(b)-peptides based on the crystal structure of I-A(d) might explain the increased stability and the preference for hydrophobic residues in this site. Taken together with what is known of the resident stability at a mildly acidic pH, the difference in stability would closely correlate with the ability of MHC class II to exchange peptides from CLIP to antigenic peptides in the endosome.

MeSH terms

  • Animals
  • Binding Sites
  • Histocompatibility Antigens Class II / chemistry*
  • Histocompatibility Antigens Class II / metabolism
  • Mice
  • Models, Molecular
  • Peptide Fragments / chemistry*
  • Protein Conformation*
  • Protein Denaturation
  • Temperature
  • Thermodynamics

Substances

  • Histocompatibility Antigens Class II
  • I-A(b) antigen, mouse
  • I-E-antigen
  • Peptide Fragments