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Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1
The ER is a key organelle of membrane biogenesis and crucial for the folding of both membrane and secretory proteins. Sensors of the unfolded protein response (UPR) monitor the unfolded protein load in the ER and convey effector functions for maintaining ER homeostasis. Aberrant compositions of the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256922/ https://www.ncbi.nlm.nih.gov/pubmed/34196665 http://dx.doi.org/10.1083/jcb.202011078 |
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author | Väth, Kristina Mattes, Carsten Reinhard, John Covino, Roberto Stumpf, Heike Hummer, Gerhard Ernst, Robert |
author_facet | Väth, Kristina Mattes, Carsten Reinhard, John Covino, Roberto Stumpf, Heike Hummer, Gerhard Ernst, Robert |
author_sort | Väth, Kristina |
collection | PubMed |
description | The ER is a key organelle of membrane biogenesis and crucial for the folding of both membrane and secretory proteins. Sensors of the unfolded protein response (UPR) monitor the unfolded protein load in the ER and convey effector functions for maintaining ER homeostasis. Aberrant compositions of the ER membrane, referred to as lipid bilayer stress, are equally potent activators of the UPR. How the distinct signals from lipid bilayer stress and unfolded proteins are processed by the conserved UPR transducer Ire1 remains unknown. Here, we have generated a functional, cysteine-less variant of Ire1 and performed systematic cysteine cross-linking experiments in native membranes to establish its transmembrane architecture in signaling-active clusters. We show that the transmembrane helices of two neighboring Ire1 molecules adopt an X-shaped configuration independent of the primary cause for ER stress. This suggests that different forms of stress converge in a common, signaling-active transmembrane architecture of Ire1. |
format | Online Article Text |
id | pubmed-8256922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82569222021-07-09 Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 Väth, Kristina Mattes, Carsten Reinhard, John Covino, Roberto Stumpf, Heike Hummer, Gerhard Ernst, Robert J Cell Biol Article The ER is a key organelle of membrane biogenesis and crucial for the folding of both membrane and secretory proteins. Sensors of the unfolded protein response (UPR) monitor the unfolded protein load in the ER and convey effector functions for maintaining ER homeostasis. Aberrant compositions of the ER membrane, referred to as lipid bilayer stress, are equally potent activators of the UPR. How the distinct signals from lipid bilayer stress and unfolded proteins are processed by the conserved UPR transducer Ire1 remains unknown. Here, we have generated a functional, cysteine-less variant of Ire1 and performed systematic cysteine cross-linking experiments in native membranes to establish its transmembrane architecture in signaling-active clusters. We show that the transmembrane helices of two neighboring Ire1 molecules adopt an X-shaped configuration independent of the primary cause for ER stress. This suggests that different forms of stress converge in a common, signaling-active transmembrane architecture of Ire1. Rockefeller University Press 2021-07-01 /pmc/articles/PMC8256922/ /pubmed/34196665 http://dx.doi.org/10.1083/jcb.202011078 Text en © 2021 Väth et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Väth, Kristina Mattes, Carsten Reinhard, John Covino, Roberto Stumpf, Heike Hummer, Gerhard Ernst, Robert Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 |
title | Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 |
title_full | Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 |
title_fullStr | Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 |
title_full_unstemmed | Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 |
title_short | Cysteine cross-linking in native membranes establishes the transmembrane architecture of Ire1 |
title_sort | cysteine cross-linking in native membranes establishes the transmembrane architecture of ire1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256922/ https://www.ncbi.nlm.nih.gov/pubmed/34196665 http://dx.doi.org/10.1083/jcb.202011078 |
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