T-CELL RECOGNITION OF IA MOLECULES SELECTIVELY ALTERED BY A SINGLE AMINO-ACID SUBSTITUTION

T lymphocytes recognize foreign antigen together with allele-specific determinants on membrane-bound class I and class II (Ia) gene products of the major histocompatibility complex. To identify amino acids of class II molecules critical to this recognition process, the genes encoding the .beta. chains of the I-Ak molecule were cloned from a wild-type B-cell hybridoma and from an immunoselected variant subline showing distinct serological and T-cell stimulatory properties. Nucleotide sequenching and DNA-mediated gene transfer established that a single base transition (G .fwdarw. A) encoding a change from glutamic acid to lysine at position 67 in the I-A.beta.k molecule accounted for all the observed phenotypic changes of the variant cells. These results confirm the importance of residues 62 to 78 in the amino terminal domain of I-A.beta.k for class II-restricted T-cell recognition of antigen and demonstrate the ability of a single substitution in this region to alter this recognition event.