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Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes
The integrin α6β4 and cytoskeletal adaptor plectin are essential components of type I and type II hemidesmosomes (HDs). We recently identified an alternative type II HD adhesion complex that also contains CD151 and the integrin α3β1. Here, we have taken a BioID proximity labeling approach to define...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438003/ https://www.ncbi.nlm.nih.gov/pubmed/32709696 http://dx.doi.org/10.1242/bio.054155 |
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author | te Molder, Lisa Hoekman, Liesbeth Kreft, Maaike Bleijerveld, Onno Sonnenberg, Arnoud |
author_facet | te Molder, Lisa Hoekman, Liesbeth Kreft, Maaike Bleijerveld, Onno Sonnenberg, Arnoud |
author_sort | te Molder, Lisa |
collection | PubMed |
description | The integrin α6β4 and cytoskeletal adaptor plectin are essential components of type I and type II hemidesmosomes (HDs). We recently identified an alternative type II HD adhesion complex that also contains CD151 and the integrin α3β1. Here, we have taken a BioID proximity labeling approach to define the proximity protein environment for α6β4 in keratinocytes. We identified 37 proteins that interacted with both α6 and β4, while 20 and 78 proteins specifically interacted with the α6 and β4 subunits, respectively. Many of the proximity interactors of α6β4 are components of focal adhesions (FAs) and the cortical microtubule stabilizing complex (CMSC). Though the close association of CMSCs with α6β4 in HDs was confirmed by immunofluorescence analysis, CMSCs have no role in the assembly of HDs. Analysis of the β4 interactome in the presence or absence of CD151 revealed that they are strikingly similar; only 11 different interactors were identified. One of these was the integrin α3β1, which interacted with α6β4 more strongly in the presence of CD151 than in its absence. These findings indicate that CD151 does not significantly contribute to the interactome of α6β4, but suggest a role of CD151 in linking α3β1 and α6β4 together in tetraspanin adhesion structures. |
format | Online Article Text |
id | pubmed-7438003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-74380032020-08-20 Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes te Molder, Lisa Hoekman, Liesbeth Kreft, Maaike Bleijerveld, Onno Sonnenberg, Arnoud Biol Open Research Article The integrin α6β4 and cytoskeletal adaptor plectin are essential components of type I and type II hemidesmosomes (HDs). We recently identified an alternative type II HD adhesion complex that also contains CD151 and the integrin α3β1. Here, we have taken a BioID proximity labeling approach to define the proximity protein environment for α6β4 in keratinocytes. We identified 37 proteins that interacted with both α6 and β4, while 20 and 78 proteins specifically interacted with the α6 and β4 subunits, respectively. Many of the proximity interactors of α6β4 are components of focal adhesions (FAs) and the cortical microtubule stabilizing complex (CMSC). Though the close association of CMSCs with α6β4 in HDs was confirmed by immunofluorescence analysis, CMSCs have no role in the assembly of HDs. Analysis of the β4 interactome in the presence or absence of CD151 revealed that they are strikingly similar; only 11 different interactors were identified. One of these was the integrin α3β1, which interacted with α6β4 more strongly in the presence of CD151 than in its absence. These findings indicate that CD151 does not significantly contribute to the interactome of α6β4, but suggest a role of CD151 in linking α3β1 and α6β4 together in tetraspanin adhesion structures. The Company of Biologists Ltd 2020-08-13 /pmc/articles/PMC7438003/ /pubmed/32709696 http://dx.doi.org/10.1242/bio.054155 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article te Molder, Lisa Hoekman, Liesbeth Kreft, Maaike Bleijerveld, Onno Sonnenberg, Arnoud Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
title | Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
title_full | Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
title_fullStr | Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
title_full_unstemmed | Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
title_short | Comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
title_sort | comparative interactomics analysis reveals potential regulators of α6β4 distribution in keratinocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438003/ https://www.ncbi.nlm.nih.gov/pubmed/32709696 http://dx.doi.org/10.1242/bio.054155 |
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