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DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region

We have produced a series of in vitro serologically selected cell lines that express mutant I-Ak molecules. In this report we describe the DNA sequence analysis of the Ak beta gene of four cell lines that express serologically altered Ak beta polypeptides in association with wild- type Ak alpha poly...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189586/
https://www.ncbi.nlm.nih.gov/pubmed/2439643
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collection PubMed
description We have produced a series of in vitro serologically selected cell lines that express mutant I-Ak molecules. In this report we describe the DNA sequence analysis of the Ak beta gene of four cell lines that express serologically altered Ak beta polypeptides in association with wild- type Ak alpha polypeptides. Each of the major serologic epitopes on the Ak beta polypeptide has been altered in one or more of the four mutants. In addition, the four mutants exhibit a broad spectrum of functional defects when used to stimulate a panel of T hybridomas of various specificities. The DNA sequence analysis revealed that each mutant had sustained a single nucleotide substitution resulting in a single amino acid substitution. All four independent substitutions occurred within or near the third of the four variable regions defined in the beta 1 domain of the A beta polypeptide by allelic comparisons. These data strongly suggest that the third variable region is the major determinant of alloantigenicity on the Ak beta polypeptide.
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spelling pubmed-21895862008-04-17 DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region J Exp Med Articles We have produced a series of in vitro serologically selected cell lines that express mutant I-Ak molecules. In this report we describe the DNA sequence analysis of the Ak beta gene of four cell lines that express serologically altered Ak beta polypeptides in association with wild- type Ak alpha polypeptides. Each of the major serologic epitopes on the Ak beta polypeptide has been altered in one or more of the four mutants. In addition, the four mutants exhibit a broad spectrum of functional defects when used to stimulate a panel of T hybridomas of various specificities. The DNA sequence analysis revealed that each mutant had sustained a single nucleotide substitution resulting in a single amino acid substitution. All four independent substitutions occurred within or near the third of the four variable regions defined in the beta 1 domain of the A beta polypeptide by allelic comparisons. These data strongly suggest that the third variable region is the major determinant of alloantigenicity on the Ak beta polypeptide. The Rockefeller University Press 1987-08-01 /pmc/articles/PMC2189586/ /pubmed/2439643 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region
title DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region
title_full DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region
title_fullStr DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region
title_full_unstemmed DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region
title_short DNA sequence analysis of I-Ak beta mutants reveals serologically immunodominant region
title_sort dna sequence analysis of i-ak beta mutants reveals serologically immunodominant region
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189586/
https://www.ncbi.nlm.nih.gov/pubmed/2439643