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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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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. |
format | Online Article Text |
id | pubmed-3565172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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