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Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules

In mice, two families of structurally distinct Ia molecules, one designated I-A and the other I-E, have been identified and characterized. The HLA-DR molecules represent one family of human Ia molecules equivalent to the murine I-E molecules on the basis of amino acid sequence homology. We describe...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186769/
https://www.ncbi.nlm.nih.gov/pubmed/6808075
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description In mice, two families of structurally distinct Ia molecules, one designated I-A and the other I-E, have been identified and characterized. The HLA-DR molecules represent one family of human Ia molecules equivalent to the murine I-E molecules on the basis of amino acid sequence homology. We describe the isolation and biochemical characterization of a second family of human Ia molecules, designated HLA-DS for second D-region locus, equivalent to the murine I-A molecules. The human HLA-DS molecules consist of two polypeptide chains, DS alpha (37,000 mol wt) and DS beta (29,000 mol wt), with 73% amino acid sequence identity to the murine I-A molecules. Furthermore, the HLA-DS molecules are closely linked genetically to HLA-DR molecules, a situation analogous to that observed in mice. The similarity in molecular weights of the DR and DS molecules might explain why others have failed to identify the latter in man.
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spelling pubmed-21867692008-04-17 Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules J Exp Med Articles In mice, two families of structurally distinct Ia molecules, one designated I-A and the other I-E, have been identified and characterized. The HLA-DR molecules represent one family of human Ia molecules equivalent to the murine I-E molecules on the basis of amino acid sequence homology. We describe the isolation and biochemical characterization of a second family of human Ia molecules, designated HLA-DS for second D-region locus, equivalent to the murine I-A molecules. The human HLA-DS molecules consist of two polypeptide chains, DS alpha (37,000 mol wt) and DS beta (29,000 mol wt), with 73% amino acid sequence identity to the murine I-A molecules. Furthermore, the HLA-DS molecules are closely linked genetically to HLA-DR molecules, a situation analogous to that observed in mice. The similarity in molecular weights of the DR and DS molecules might explain why others have failed to identify the latter in man. The Rockefeller University Press 1982-08-01 /pmc/articles/PMC2186769/ /pubmed/6808075 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
Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules
title Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules
title_full Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules
title_fullStr Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules
title_full_unstemmed Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules
title_short Biochemical characterization of a second family of human Ia molecules, HLA-DS, equivalent to murine I-A subregion molecules
title_sort biochemical characterization of a second family of human ia molecules, hla-ds, equivalent to murine i-a subregion molecules
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186769/
https://www.ncbi.nlm.nih.gov/pubmed/6808075