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The specificity of homomeric clustering of CD81 is mediated by its δ‐loop
Tetraspanins are cell membrane‐scaffolding proteins interacting with one another and a repertoire of interaction partners. Through these interactions, they form extended molecular networks as tetraspanin webs or tetraspanin‐enriched microdomains. Microscopic data suggest that these networks contain...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292664/ https://www.ncbi.nlm.nih.gov/pubmed/28174692 http://dx.doi.org/10.1002/2211-5463.12187 |
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author | Homsi, Yahya Lang, Thorsten |
author_facet | Homsi, Yahya Lang, Thorsten |
author_sort | Homsi, Yahya |
collection | PubMed |
description | Tetraspanins are cell membrane‐scaffolding proteins interacting with one another and a repertoire of interaction partners. Through these interactions, they form extended molecular networks as tetraspanin webs or tetraspanin‐enriched microdomains. Microscopic data suggest that these networks contain tetraspanin clusters, with poor overlap between clusters formed by different tetraspanins. Here, we investigate the possibility of targeting tetraspanins CD9 or CD151 to clusters formed by the tetraspanin CD81. We find that the δ‐loop from the large extracellular domain of CD81 is sufficient for targeting of CD9/CD151 to CD81 clusters. Moreover, in a pull‐down assay, CD9 coprecipitates more CD81 when it carries the CD81 δ‐loop. In conclusion, the information for forming homomeric CD81 clusters is encoded in the δ‐loop. |
format | Online Article Text |
id | pubmed-5292664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52926642017-02-07 The specificity of homomeric clustering of CD81 is mediated by its δ‐loop Homsi, Yahya Lang, Thorsten FEBS Open Bio Research Articles Tetraspanins are cell membrane‐scaffolding proteins interacting with one another and a repertoire of interaction partners. Through these interactions, they form extended molecular networks as tetraspanin webs or tetraspanin‐enriched microdomains. Microscopic data suggest that these networks contain tetraspanin clusters, with poor overlap between clusters formed by different tetraspanins. Here, we investigate the possibility of targeting tetraspanins CD9 or CD151 to clusters formed by the tetraspanin CD81. We find that the δ‐loop from the large extracellular domain of CD81 is sufficient for targeting of CD9/CD151 to CD81 clusters. Moreover, in a pull‐down assay, CD9 coprecipitates more CD81 when it carries the CD81 δ‐loop. In conclusion, the information for forming homomeric CD81 clusters is encoded in the δ‐loop. John Wiley and Sons Inc. 2017-01-19 /pmc/articles/PMC5292664/ /pubmed/28174692 http://dx.doi.org/10.1002/2211-5463.12187 Text en © 2016 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Homsi, Yahya Lang, Thorsten The specificity of homomeric clustering of CD81 is mediated by its δ‐loop |
title | The specificity of homomeric clustering of CD81 is mediated by its δ‐loop |
title_full | The specificity of homomeric clustering of CD81 is mediated by its δ‐loop |
title_fullStr | The specificity of homomeric clustering of CD81 is mediated by its δ‐loop |
title_full_unstemmed | The specificity of homomeric clustering of CD81 is mediated by its δ‐loop |
title_short | The specificity of homomeric clustering of CD81 is mediated by its δ‐loop |
title_sort | specificity of homomeric clustering of cd81 is mediated by its δ‐loop |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292664/ https://www.ncbi.nlm.nih.gov/pubmed/28174692 http://dx.doi.org/10.1002/2211-5463.12187 |
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