Single-residue changes in class I major histocompatibility complex molecules stimulate responses to self peptides
- PMID: 1557385
- PMCID: PMC48749
- DOI: 10.1073/pnas.89.7.2794
Single-residue changes in class I major histocompatibility complex molecules stimulate responses to self peptides
Abstract
Single-residue changes were introduced into the murine major histocompatibility complex class I molecule H-2Kb at positions 65 and 69, which are predicted to point up from the alpha-helix of the alpha 1 domain and not into the peptide binding groove. Mutated and wild-type genes were transfected into the murine cell line P815 (H-2d). We present evidence that the changes did not affect the binding of three foreign peptides that are recognized by cytotoxic T lymphocytes (CTL) in association with H-2Kb. Additionally, the mutants provoked strong alloreactive responses in T cells from mice expressing unmutated H-2Kb. The alloreactive CTL were specific for self peptides, which could be extracted from wild-type H-2Kb molecules, recognized in the context of the mutant class I.
Similar articles
-
A viral peptide can mimic an endogenous peptide for allorecognition of a major histocompatibility complex class I product.Eur J Immunol. 1992 Jun;22(6):1651-4. doi: 10.1002/eji.1830220647. Eur J Immunol. 1992. PMID: 1318201
-
Inhibition of allorecognition by an H-2Kb-derived peptide is evidence for a T-cell binding region on a major histocompatibility complex molecule.Proc Natl Acad Sci U S A. 1989 Nov;86(21):8516-20. doi: 10.1073/pnas.86.21.8516. Proc Natl Acad Sci U S A. 1989. PMID: 2813409 Free PMC article.
-
Minor pocket B influences peptide binding, peptide presentation and alloantigenicity of H-2Kb.Int Immunol. 1994 Jul;6(7):1037-47. doi: 10.1093/intimm/6.7.1037. Int Immunol. 1994. PMID: 7947455
-
Class I antigen presentation.Year Immunol. 1989;4:41-58. Year Immunol. 1989. PMID: 2522701 Review. No abstract available.
-
Mechanisms of T cell recognition of alloantigen. The role of peptides.Transplantation. 1994 May 15;57(9):1295-302. doi: 10.1097/00007890-199405150-00001. Transplantation. 1994. PMID: 8184464 Review. No abstract available.
Cited by
-
Conformational differences in major histocompatibility complex-peptide complexes can result in alloreactivity.J Exp Med. 1994 Jan 1;179(1):213-9. doi: 10.1084/jem.179.1.213. J Exp Med. 1994. PMID: 8270866 Free PMC article.
-
Cells infected with Yersinia present an epitope to class I MHC-restricted CTL.J Immunol. 1994 Aug 15;153(4):1603-12. J Immunol. 1994. PMID: 8046234 Free PMC article.
-
Correlated evolution of nucleotide substitution rates and allelic variation in Mhc-DRB lineages of primates.BMC Evol Biol. 2009 Apr 12;9:73. doi: 10.1186/1471-2148-9-73. BMC Evol Biol. 2009. PMID: 19361342 Free PMC article.
-
The role of peptides in T cell alloreactivity is determined by self-major histocompatibility complex molecules.J Exp Med. 2000 Mar 6;191(5):805-12. doi: 10.1084/jem.191.5.805. J Exp Med. 2000. PMID: 10704462 Free PMC article.
-
T cell receptor (TCR) recognition of MHC class I variants: intermolecular second-site reversion provides evidence for peptide/MHC conformational variation.J Exp Med. 1996 Jul 1;184(1):253-8. doi: 10.1084/jem.184.1.253. J Exp Med. 1996. PMID: 8691139 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources