Direct demonstration of critical amino acid residues required for cytotoxic T-lymphocyte allorecognition of H-2 class I antigens
- PMID: 2452442
- PMCID: PMC280148
- DOI: 10.1073/pnas.85.9.3085
Direct demonstration of critical amino acid residues required for cytotoxic T-lymphocyte allorecognition of H-2 class I antigens
Abstract
To identify critical amino acid residues recognized by alloreactive cytolytic T lymphocytes (CTL) generated between H-2Kb and H-2Kbm1, we have derived a series of cloned L-cell lines expressing the following mutant H-2Kb class I genes. Cell line L-KbTyr-Tyr expresses a mutant gene in which positions 155-156 of the Kb molecule have been changed from Arg-Leu to Tyr-Tyr, leaving position 152 unchanged. Cell line L-KbAla expresses the reciprocal mutant gene that has position 152 of the Kb molecule mutated from glutamic acid to alanine, leaving positions 155-156 unchanged. Electrophoretic mobilities of the mutant Kb molecules reflect only those changes predicted by the mutations. Mutant-specific (anti-Kbm1) and native-specific (anti-Kb) CTL lyse L-KbTyr-Tyr and L-KbAla target cells equally well. Unlabeled target inhibition of lysis revealed a pattern of recognition and inhibition that suggests that the amino acid differences between Kbm1 and Kb create at least two discrete determinants that can be recognized by different populations of CTL. The results suggest that these determinants consist, at least in part, of a linear amino acid sequence from which critical amino acid residues can be identified.
Similar articles
-
An immunodominant epitope present in multiple class I MHC molecules and recognized by cytotoxic T lymphocytes.J Exp Med. 1988 Jul 1;168(1):307-24. doi: 10.1084/jem.168.1.307. J Exp Med. 1988. PMID: 2456370 Free PMC article.
-
Recognition of H-2Kb mutant target cells by Moloney virus-specific cytotoxic T lymphocytes from bm13 (H-2Db-mutant) mice. II. Relationship of Kbm3 and Kbm11 in restriction specificities and allodeterminants.J Immunol. 1984 Jul;133(1):28-32. J Immunol. 1984. PMID: 6202783
-
Introduction of H-2Dd determinants into the H-2Ld antigen by site-directed mutagenesis.J Exp Med. 1987 Sep 1;166(3):744-60. doi: 10.1084/jem.166.3.744. J Exp Med. 1987. PMID: 2442290 Free PMC article.
-
Presentation of a horse cytochrome c peptide by multiple H-2b class I major histocompatibility complex (MHC) molecules to C57BL/6- and bm1-derived cytotoxic T lymphocytes: presence of a single MHC anchor residue may confer efficient peptide-specific CTL recognition.Eur J Immunol. 1994 Sep;24(9):2141-9. doi: 10.1002/eji.1830240931. Eur J Immunol. 1994. PMID: 7522163
-
Murine major histocompatibility complex class-I mutants: molecular analysis and structure-function implications.Annu Rev Immunol. 1986;4:471-502. doi: 10.1146/annurev.iy.04.040186.002351. Annu Rev Immunol. 1986. PMID: 3518748 Review.
Cited by
-
Mutations inside but not outside the peptide binding cleft of the H-2 Ld molecule affect CTL recognition and binding of the nucleoprotein peptide from the lymphocytic choriomeningitis virus.Immunogenetics. 1994;40(3):222-9. doi: 10.1007/BF00167083. Immunogenetics. 1994. PMID: 7518804
-
An immunodominant epitope present in multiple class I MHC molecules and recognized by cytotoxic T lymphocytes.J Exp Med. 1988 Jul 1;168(1):307-24. doi: 10.1084/jem.168.1.307. J Exp Med. 1988. PMID: 2456370 Free PMC article.
-
I-A alpha polymorphic residues that determine alloreactive T cell recognition.J Exp Med. 1989 May 1;169(5):1655-68. doi: 10.1084/jem.169.5.1655. J Exp Med. 1989. PMID: 2469763 Free PMC article.
-
Analysis of novel residues of class I involved in recognition by alloreactive T cells.Immunogenetics. 1990;32(2):138-41. doi: 10.1007/BF00210452. Immunogenetics. 1990. PMID: 2397933 No abstract available.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources