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An optical assay of the transport activity of ClC-7

Osteoporosis, characterized by excessive osteoclast mediated bone resorption, affects millions of people worldwide representing a major public health problem. ClC-7 is a chloride-proton exchanger localized in lysosomes and in the resorption lacuna in osteoclasts where it is essential for bone resorp...

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Autores principales: Zanardi, Ilaria, Zifarelli, Giovanni, Pusch, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565172/
https://www.ncbi.nlm.nih.gov/pubmed/23390581
http://dx.doi.org/10.1038/srep01231
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author Zanardi, Ilaria
Zifarelli, Giovanni
Pusch, Michael
author_facet Zanardi, Ilaria
Zifarelli, Giovanni
Pusch, Michael
author_sort Zanardi, Ilaria
collection PubMed
description Osteoporosis, characterized by excessive osteoclast mediated bone resorption, affects millions of people worldwide representing a major public health problem. ClC-7 is a chloride-proton exchanger localized in lysosomes and in the resorption lacuna in osteoclasts where it is essential for bone resorption. Thus, drugs targeted at ClC-7 have been proposed for ameliorating osteoporosis. However, functional assays suited for high throughput screening (HTS) of ClC-7 function are lacking. Here we describe two complementary variants of purely optical assays of the transport activity of ClC-7, redirected to the plasma membrane employing a genetically encoded fluorescent Cl(−)/pH indicator fused to the ClC-7 protein. These simple and robust functional assays of ClC-7 transport are well-suited to be applied in HTS of small-molecule inhibitors and may help to develop drugs suited for the treatment of osteoporosis.
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spelling pubmed-35651722013-02-06 An optical assay of the transport activity of ClC-7 Zanardi, Ilaria Zifarelli, Giovanni Pusch, Michael Sci Rep Article Osteoporosis, characterized by excessive osteoclast mediated bone resorption, affects millions of people worldwide representing a major public health problem. ClC-7 is a chloride-proton exchanger localized in lysosomes and in the resorption lacuna in osteoclasts where it is essential for bone resorption. Thus, drugs targeted at ClC-7 have been proposed for ameliorating osteoporosis. However, functional assays suited for high throughput screening (HTS) of ClC-7 function are lacking. Here we describe two complementary variants of purely optical assays of the transport activity of ClC-7, redirected to the plasma membrane employing a genetically encoded fluorescent Cl(−)/pH indicator fused to the ClC-7 protein. These simple and robust functional assays of ClC-7 transport are well-suited to be applied in HTS of small-molecule inhibitors and may help to develop drugs suited for the treatment of osteoporosis. Nature Publishing Group 2013-02-06 /pmc/articles/PMC3565172/ /pubmed/23390581 http://dx.doi.org/10.1038/srep01231 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Zanardi, Ilaria
Zifarelli, Giovanni
Pusch, Michael
An optical assay of the transport activity of ClC-7
title An optical assay of the transport activity of ClC-7
title_full An optical assay of the transport activity of ClC-7
title_fullStr An optical assay of the transport activity of ClC-7
title_full_unstemmed An optical assay of the transport activity of ClC-7
title_short An optical assay of the transport activity of ClC-7
title_sort optical assay of the transport activity of clc-7
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565172/
https://www.ncbi.nlm.nih.gov/pubmed/23390581
http://dx.doi.org/10.1038/srep01231
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