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Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox

Interfering with disulfide bond formation impedes protein folding and promotes endoplasmic reticulum (ER) stress. Due to limitations in measurement techniques, the relationships of altered thiol redox and ER stress have been difficult to assess. We report that fluorescent lifetime measurements circu...

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Autores principales: Avezov, Edward, Cross, Benedict C.S., Kaminski Schierle, Gabriele S., Winters, Mikael, Harding, Heather P., Melo, Eduardo Pinho, Kaminski, Clemens F., Ron, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628511/
https://www.ncbi.nlm.nih.gov/pubmed/23589496
http://dx.doi.org/10.1083/jcb.201211155
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author Avezov, Edward
Cross, Benedict C.S.
Kaminski Schierle, Gabriele S.
Winters, Mikael
Harding, Heather P.
Melo, Eduardo Pinho
Kaminski, Clemens F.
Ron, David
author_facet Avezov, Edward
Cross, Benedict C.S.
Kaminski Schierle, Gabriele S.
Winters, Mikael
Harding, Heather P.
Melo, Eduardo Pinho
Kaminski, Clemens F.
Ron, David
author_sort Avezov, Edward
collection PubMed
description Interfering with disulfide bond formation impedes protein folding and promotes endoplasmic reticulum (ER) stress. Due to limitations in measurement techniques, the relationships of altered thiol redox and ER stress have been difficult to assess. We report that fluorescent lifetime measurements circumvented the crippling dimness of an ER-tuned fluorescent redox-responsive probe (roGFPiE), faithfully tracking the activity of the major ER-localized protein disulfide isomerase, PDI. In vivo lifetime imaging by time-correlated single-photon counting (TCSPC) recorded subtle changes in ER redox poise induced by exposure of mammalian cells to a reducing environment but revealed an unanticipated stability of redox to fluctuations in unfolded protein load. By contrast, TCSPC of roGFPiE uncovered a hitherto unsuspected reductive shift in the mammalian ER upon loss of luminal calcium, whether induced by pharmacological inhibition of calcium reuptake into the ER or by physiological activation of release channels. These findings recommend fluorescent lifetime imaging as a sensitive method to track ER redox homeostasis in mammalian cells.
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spelling pubmed-36285112013-10-15 Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox Avezov, Edward Cross, Benedict C.S. Kaminski Schierle, Gabriele S. Winters, Mikael Harding, Heather P. Melo, Eduardo Pinho Kaminski, Clemens F. Ron, David J Cell Biol Research Articles Interfering with disulfide bond formation impedes protein folding and promotes endoplasmic reticulum (ER) stress. Due to limitations in measurement techniques, the relationships of altered thiol redox and ER stress have been difficult to assess. We report that fluorescent lifetime measurements circumvented the crippling dimness of an ER-tuned fluorescent redox-responsive probe (roGFPiE), faithfully tracking the activity of the major ER-localized protein disulfide isomerase, PDI. In vivo lifetime imaging by time-correlated single-photon counting (TCSPC) recorded subtle changes in ER redox poise induced by exposure of mammalian cells to a reducing environment but revealed an unanticipated stability of redox to fluctuations in unfolded protein load. By contrast, TCSPC of roGFPiE uncovered a hitherto unsuspected reductive shift in the mammalian ER upon loss of luminal calcium, whether induced by pharmacological inhibition of calcium reuptake into the ER or by physiological activation of release channels. These findings recommend fluorescent lifetime imaging as a sensitive method to track ER redox homeostasis in mammalian cells. The Rockefeller University Press 2013-04-15 /pmc/articles/PMC3628511/ /pubmed/23589496 http://dx.doi.org/10.1083/jcb.201211155 Text en © 2013 Avezov et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Avezov, Edward
Cross, Benedict C.S.
Kaminski Schierle, Gabriele S.
Winters, Mikael
Harding, Heather P.
Melo, Eduardo Pinho
Kaminski, Clemens F.
Ron, David
Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox
title Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox
title_full Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox
title_fullStr Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox
title_full_unstemmed Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox
title_short Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox
title_sort lifetime imaging of a fluorescent protein sensor reveals surprising stability of er thiol redox
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628511/
https://www.ncbi.nlm.nih.gov/pubmed/23589496
http://dx.doi.org/10.1083/jcb.201211155
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