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Class I molecules retained in the endoplasmic reticulum bind antigenic peptides
We isolated major histocompatibility complex (MHC)-specific viral peptides from cells infected with influenza virus in the continuous presence of the drug brefeldin A, which blocks exocytosis of newly synthesized MHC class I molecules. MHC-specific peptides were also isolated from cells expressing m...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1993
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191061/ https://www.ncbi.nlm.nih.gov/pubmed/8496682 |
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collection | PubMed |
description | We isolated major histocompatibility complex (MHC)-specific viral peptides from cells infected with influenza virus in the continuous presence of the drug brefeldin A, which blocks exocytosis of newly synthesized MHC class I molecules. MHC-specific peptides were also isolated from cells expressing mouse Kd class I MHC molecules whose cytoplasmic domain was substituted by that of the adenovirus E3/19K glycoprotein. This molecule was retained in an intracellular pre-Golgi complex compartment as demonstrated by immunocytochemical and biochemical means. Since we show that intracellular association of antigenic peptides with such retained class I molecules is necessary for their isolation from cellular extracts, this provides direct evidence that naturally processed peptides associate with class I MHC molecules in an early intracellular exocytic compartment. |
format | Text |
id | pubmed-2191061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21910612008-04-16 Class I molecules retained in the endoplasmic reticulum bind antigenic peptides J Exp Med Articles We isolated major histocompatibility complex (MHC)-specific viral peptides from cells infected with influenza virus in the continuous presence of the drug brefeldin A, which blocks exocytosis of newly synthesized MHC class I molecules. MHC-specific peptides were also isolated from cells expressing mouse Kd class I MHC molecules whose cytoplasmic domain was substituted by that of the adenovirus E3/19K glycoprotein. This molecule was retained in an intracellular pre-Golgi complex compartment as demonstrated by immunocytochemical and biochemical means. Since we show that intracellular association of antigenic peptides with such retained class I molecules is necessary for their isolation from cellular extracts, this provides direct evidence that naturally processed peptides associate with class I MHC molecules in an early intracellular exocytic compartment. The Rockefeller University Press 1993-06-01 /pmc/articles/PMC2191061/ /pubmed/8496682 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 Class I molecules retained in the endoplasmic reticulum bind antigenic peptides |
title | Class I molecules retained in the endoplasmic reticulum bind antigenic peptides |
title_full | Class I molecules retained in the endoplasmic reticulum bind antigenic peptides |
title_fullStr | Class I molecules retained in the endoplasmic reticulum bind antigenic peptides |
title_full_unstemmed | Class I molecules retained in the endoplasmic reticulum bind antigenic peptides |
title_short | Class I molecules retained in the endoplasmic reticulum bind antigenic peptides |
title_sort | class i molecules retained in the endoplasmic reticulum bind antigenic peptides |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191061/ https://www.ncbi.nlm.nih.gov/pubmed/8496682 |