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TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9)
Both superantigens (SAG) and many anti-TCR monoclonal antibodies (mAb) have specificity for the V beta region of the TCR encoded by TCRBV genes. For instance the bacterial SAG staphylococcal enterotoxin E (SEE), the retroviral SAG MTV-9 and the mAb OT145 each react with human T cells expressing BV6S...
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Lenguaje: | English |
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The Rockefeller University Press
1996
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192839/ https://www.ncbi.nlm.nih.gov/pubmed/8879218 |
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collection | PubMed |
description | Both superantigens (SAG) and many anti-TCR monoclonal antibodies (mAb) have specificity for the V beta region of the TCR encoded by TCRBV genes. For instance the bacterial SAG staphylococcal enterotoxin E (SEE), the retroviral SAG MTV-9 and the mAb OT145 each react with human T cells expressing BV6S7. This BV gene encodes two common alleles. We found that SEE and the mAb preferentially activate T cells expressing BV6S7*1 as opposed to BV6S7*2, but Mtv-9 activates T cells expressing either allele. Thus binding to the TCR differs between the two SAGs. A mutation in the TCR HVR-4 region of BV6S7*1 (G72E), where the two BV6S7 alleles differ, indicated that HVR-4 is a component of the binding site for SEE and for the mAb OT145. BV6S7*2 has a charged E72 which may result in electrostatic repulsion of SEE, as SEE contains a similarly acidic aspartic acid residue at a TCR interaction site (204D). |
format | Text |
id | pubmed-2192839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21928392008-04-16 TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) J Exp Med Articles Both superantigens (SAG) and many anti-TCR monoclonal antibodies (mAb) have specificity for the V beta region of the TCR encoded by TCRBV genes. For instance the bacterial SAG staphylococcal enterotoxin E (SEE), the retroviral SAG MTV-9 and the mAb OT145 each react with human T cells expressing BV6S7. This BV gene encodes two common alleles. We found that SEE and the mAb preferentially activate T cells expressing BV6S7*1 as opposed to BV6S7*2, but Mtv-9 activates T cells expressing either allele. Thus binding to the TCR differs between the two SAGs. A mutation in the TCR HVR-4 region of BV6S7*1 (G72E), where the two BV6S7 alleles differ, indicated that HVR-4 is a component of the binding site for SEE and for the mAb OT145. BV6S7*2 has a charged E72 which may result in electrostatic repulsion of SEE, as SEE contains a similarly acidic aspartic acid residue at a TCR interaction site (204D). The Rockefeller University Press 1996-10-01 /pmc/articles/PMC2192839/ /pubmed/8879218 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 TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) |
title | TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) |
title_full | TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) |
title_fullStr | TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) |
title_full_unstemmed | TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) |
title_short | TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9) |
title_sort | tcr binding differs for a bacterial superantigen (see) and a viral superantigen (mtv-9) |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192839/ https://www.ncbi.nlm.nih.gov/pubmed/8879218 |