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Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor

Distinct spatiotemporal Ca(2+) signalling events regulate fundamental aspects of eukaryotic cell physiology. Complex Ca(2+) signals can be driven by release of Ca(2+) from intracellular organelles that sequester Ca(2+) such as the ER (endoplasmic reticulum) or through the opening of Ca(2+)-permeable...

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Autores principales: McCue, Hannah V., Wardyn, Joanna D., Burgoyne, Robert D., Haynes, Lee P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526116/
https://www.ncbi.nlm.nih.gov/pubmed/23098255
http://dx.doi.org/10.1042/BJ20120898
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author McCue, Hannah V.
Wardyn, Joanna D.
Burgoyne, Robert D.
Haynes, Lee P.
author_facet McCue, Hannah V.
Wardyn, Joanna D.
Burgoyne, Robert D.
Haynes, Lee P.
author_sort McCue, Hannah V.
collection PubMed
description Distinct spatiotemporal Ca(2+) signalling events regulate fundamental aspects of eukaryotic cell physiology. Complex Ca(2+) signals can be driven by release of Ca(2+) from intracellular organelles that sequester Ca(2+) such as the ER (endoplasmic reticulum) or through the opening of Ca(2+)-permeable channels in the plasma membrane and influx of extracellular Ca(2+). Late endocytic pathway compartments including late-endosomes and lysosomes have recently been observed to sequester Ca(2+) to levels comparable with those found within the ER lumen. These organelles harbour ligand-gated Ca(2+)-release channels and evidence indicates that they can operate as Ca(2+)-signalling platforms. Lysosomes sequester Ca(2+) to a greater extent than any other endocytic compartment, and signalling from this organelle has been postulated to provide ‘trigger’ release events that can subsequently elicit more extensive Ca(2+) signals from stores including the ER. In order to investigate lysosomal-specific Ca(2+) signalling a simple method for measuring lysosomal Ca(2+) release is essential. In the present study we describe the generation and characterization of a genetically encoded, lysosomally targeted, cameleon sensor which is capable of registering specific Ca(2+) release in response to extracellular agonists and intracellular second messengers. This probe represents a novel tool that will permit detailed investigations examining the impact of lysosomal Ca(2+) handling on cellular physiology.
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spelling pubmed-35261162012-12-19 Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor McCue, Hannah V. Wardyn, Joanna D. Burgoyne, Robert D. Haynes, Lee P. Biochem J Research Article Distinct spatiotemporal Ca(2+) signalling events regulate fundamental aspects of eukaryotic cell physiology. Complex Ca(2+) signals can be driven by release of Ca(2+) from intracellular organelles that sequester Ca(2+) such as the ER (endoplasmic reticulum) or through the opening of Ca(2+)-permeable channels in the plasma membrane and influx of extracellular Ca(2+). Late endocytic pathway compartments including late-endosomes and lysosomes have recently been observed to sequester Ca(2+) to levels comparable with those found within the ER lumen. These organelles harbour ligand-gated Ca(2+)-release channels and evidence indicates that they can operate as Ca(2+)-signalling platforms. Lysosomes sequester Ca(2+) to a greater extent than any other endocytic compartment, and signalling from this organelle has been postulated to provide ‘trigger’ release events that can subsequently elicit more extensive Ca(2+) signals from stores including the ER. In order to investigate lysosomal-specific Ca(2+) signalling a simple method for measuring lysosomal Ca(2+) release is essential. In the present study we describe the generation and characterization of a genetically encoded, lysosomally targeted, cameleon sensor which is capable of registering specific Ca(2+) release in response to extracellular agonists and intracellular second messengers. This probe represents a novel tool that will permit detailed investigations examining the impact of lysosomal Ca(2+) handling on cellular physiology. Portland Press Ltd. 2012-12-14 2013-01-15 /pmc/articles/PMC3526116/ /pubmed/23098255 http://dx.doi.org/10.1042/BJ20120898 Text en © 2013 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by-nc/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
McCue, Hannah V.
Wardyn, Joanna D.
Burgoyne, Robert D.
Haynes, Lee P.
Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
title Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
title_full Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
title_fullStr Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
title_full_unstemmed Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
title_short Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
title_sort generation and characterization of a lysosomally targeted, genetically encoded ca(2+)-sensor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526116/
https://www.ncbi.nlm.nih.gov/pubmed/23098255
http://dx.doi.org/10.1042/BJ20120898
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