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Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes
The ability to generate specific cytotoxic responses using purified major histocompatibility complex (MHC) antigen in liposomes has made it possible to directly assess the importance of class I carbohydrate moieties in T cell recognition of alloantigen. Deglycosylation of affinity-purified H-2Kk to...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1985
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187872/ https://www.ncbi.nlm.nih.gov/pubmed/3876403 |
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collection | PubMed |
description | The ability to generate specific cytotoxic responses using purified major histocompatibility complex (MHC) antigen in liposomes has made it possible to directly assess the importance of class I carbohydrate moieties in T cell recognition of alloantigen. Deglycosylation of affinity-purified H-2Kk to yield a single glycan-free product did not alter the specificity, the magnitude, nor the dose range of the cytotoxic T lymphocyte (CTL) response to the class I antigen. It can be concluded that carbohydrate moieties are not required to maintain the necessary conformation of the MHC protein, nor to interact with either the antigen-specific receptor or accessory proteins on precursor CTL. |
format | Text |
id | pubmed-2187872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21878722008-04-17 Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes J Exp Med Articles The ability to generate specific cytotoxic responses using purified major histocompatibility complex (MHC) antigen in liposomes has made it possible to directly assess the importance of class I carbohydrate moieties in T cell recognition of alloantigen. Deglycosylation of affinity-purified H-2Kk to yield a single glycan-free product did not alter the specificity, the magnitude, nor the dose range of the cytotoxic T lymphocyte (CTL) response to the class I antigen. It can be concluded that carbohydrate moieties are not required to maintain the necessary conformation of the MHC protein, nor to interact with either the antigen-specific receptor or accessory proteins on precursor CTL. The Rockefeller University Press 1985-10-01 /pmc/articles/PMC2187872/ /pubmed/3876403 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 Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes |
title | Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes |
title_full | Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes |
title_fullStr | Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes |
title_full_unstemmed | Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes |
title_short | Carbohydrate moieties of major histocompatibility complex class I alloantigens are not required for their recognition by T lymphocytes |
title_sort | carbohydrate moieties of major histocompatibility complex class i alloantigens are not required for their recognition by t lymphocytes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187872/ https://www.ncbi.nlm.nih.gov/pubmed/3876403 |