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SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis
Endoplasmic reticulum (ER) calcium homeostasis is disrupted in diverse pathologies, including neurodegeneration, cardiovascular diseases, and diabetes. Temporally defining calcium dysregulation during disease progression, however, has been challenging. Here we describe secreted ER calcium-monitoring...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161517/ https://www.ncbi.nlm.nih.gov/pubmed/25031430 http://dx.doi.org/10.1091/mbc.E14-06-1141 |
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author | Henderson, Mark J. Wires, Emily S. Trychta, Kathleen A. Richie, Christopher T. Harvey, Brandon K. |
author_facet | Henderson, Mark J. Wires, Emily S. Trychta, Kathleen A. Richie, Christopher T. Harvey, Brandon K. |
author_sort | Henderson, Mark J. |
collection | PubMed |
description | Endoplasmic reticulum (ER) calcium homeostasis is disrupted in diverse pathologies, including neurodegeneration, cardiovascular diseases, and diabetes. Temporally defining calcium dysregulation during disease progression, however, has been challenging. Here we describe secreted ER calcium-monitoring proteins (SERCaMPs), which allow for longitudinal monitoring of ER calcium homeostasis. We identified a carboxy-terminal modification that is sufficient to confer release of a protein specifically in response to ER calcium depletion. A Gaussia luciferase (GLuc)–based SERCaMP provides a simple and sensitive method to monitor ER calcium homeostasis in vitro or in vivo by analyzing culture medium or blood. GLuc-SERCaMPs revealed ER calcium depletion in rat primary neurons exposed to various ER stressors. In vivo, ER calcium disruption in rat liver was monitored over several days by repeated sampling of blood. Our results suggest that SERCaMPs will have broad applications for the long-term monitoring of ER calcium homeostasis and the development of therapeutic approaches to counteract ER calcium dysregulation. |
format | Online Article Text |
id | pubmed-4161517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41615172014-11-30 SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis Henderson, Mark J. Wires, Emily S. Trychta, Kathleen A. Richie, Christopher T. Harvey, Brandon K. Mol Biol Cell Articles Endoplasmic reticulum (ER) calcium homeostasis is disrupted in diverse pathologies, including neurodegeneration, cardiovascular diseases, and diabetes. Temporally defining calcium dysregulation during disease progression, however, has been challenging. Here we describe secreted ER calcium-monitoring proteins (SERCaMPs), which allow for longitudinal monitoring of ER calcium homeostasis. We identified a carboxy-terminal modification that is sufficient to confer release of a protein specifically in response to ER calcium depletion. A Gaussia luciferase (GLuc)–based SERCaMP provides a simple and sensitive method to monitor ER calcium homeostasis in vitro or in vivo by analyzing culture medium or blood. GLuc-SERCaMPs revealed ER calcium depletion in rat primary neurons exposed to various ER stressors. In vivo, ER calcium disruption in rat liver was monitored over several days by repeated sampling of blood. Our results suggest that SERCaMPs will have broad applications for the long-term monitoring of ER calcium homeostasis and the development of therapeutic approaches to counteract ER calcium dysregulation. The American Society for Cell Biology 2014-09-15 /pmc/articles/PMC4161517/ /pubmed/25031430 http://dx.doi.org/10.1091/mbc.E14-06-1141 Text en © 2014 Henderson et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Henderson, Mark J. Wires, Emily S. Trychta, Kathleen A. Richie, Christopher T. Harvey, Brandon K. SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis |
title | SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis |
title_full | SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis |
title_fullStr | SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis |
title_full_unstemmed | SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis |
title_short | SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis |
title_sort | sercamp: a carboxy-terminal protein modification that enables monitoring of er calcium homeostasis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161517/ https://www.ncbi.nlm.nih.gov/pubmed/25031430 http://dx.doi.org/10.1091/mbc.E14-06-1141 |
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