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Mutations defining functional regions of the superantigen staphylococcal enterotoxin B
Staphylococcal enterotoxin B (SEB) is both a superantigen and toxin. As a superantigen, SEB can bind to major histocompatibility complex (MHC) class II molecules to form a ligand for alpha/beta T cell receptors bearing particular V beta elements. As a toxin, SEB causes rapid weight loss in mice some...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1992
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119125/ https://www.ncbi.nlm.nih.gov/pubmed/1370682 |
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collection | PubMed |
description | Staphylococcal enterotoxin B (SEB) is both a superantigen and toxin. As a superantigen, SEB can bind to major histocompatibility complex (MHC) class II molecules to form a ligand for alpha/beta T cell receptors bearing particular V beta elements. As a toxin, SEB causes rapid weight loss in mice sometimes leading to death. We show here that both of these functions map to the NH2-terminal portion of the toxin. Three regions were identified: one important in MHC class II binding, one in T cell recognition, and one in both functions. These results support the conclusion that the toxicity of SEB is related to massive T cell stimulation and release of cytokine mediators and show that the residues interacting with MHC and the T cell receptor are intertwined. |
format | Text |
id | pubmed-2119125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21191252008-04-16 Mutations defining functional regions of the superantigen staphylococcal enterotoxin B J Exp Med Articles Staphylococcal enterotoxin B (SEB) is both a superantigen and toxin. As a superantigen, SEB can bind to major histocompatibility complex (MHC) class II molecules to form a ligand for alpha/beta T cell receptors bearing particular V beta elements. As a toxin, SEB causes rapid weight loss in mice sometimes leading to death. We show here that both of these functions map to the NH2-terminal portion of the toxin. Three regions were identified: one important in MHC class II binding, one in T cell recognition, and one in both functions. These results support the conclusion that the toxicity of SEB is related to massive T cell stimulation and release of cytokine mediators and show that the residues interacting with MHC and the T cell receptor are intertwined. The Rockefeller University Press 1992-02-01 /pmc/articles/PMC2119125/ /pubmed/1370682 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 Mutations defining functional regions of the superantigen staphylococcal enterotoxin B |
title | Mutations defining functional regions of the superantigen staphylococcal enterotoxin B |
title_full | Mutations defining functional regions of the superantigen staphylococcal enterotoxin B |
title_fullStr | Mutations defining functional regions of the superantigen staphylococcal enterotoxin B |
title_full_unstemmed | Mutations defining functional regions of the superantigen staphylococcal enterotoxin B |
title_short | Mutations defining functional regions of the superantigen staphylococcal enterotoxin B |
title_sort | mutations defining functional regions of the superantigen staphylococcal enterotoxin b |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119125/ https://www.ncbi.nlm.nih.gov/pubmed/1370682 |