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A Generic Platform for Cellular Screening Against Ubiquitin Ligases
Ubiquitin signalling regulates most aspects of cellular life, thus deregulation of ubiquitylation has been linked with a number of diseases. E3 ubiquitin ligases provide substrate selectivity in ubiquitylation cascades and are therefore considered to be attractive targets for developing therapeutic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705515/ https://www.ncbi.nlm.nih.gov/pubmed/26743172 http://dx.doi.org/10.1038/srep18940 |
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author | Maculins, Timurs Carter, Nikki Dorval, Thierry Hudson, Kevin Nissink, J. Willem M. Hay, Ronald T. Alwan, Husam |
author_facet | Maculins, Timurs Carter, Nikki Dorval, Thierry Hudson, Kevin Nissink, J. Willem M. Hay, Ronald T. Alwan, Husam |
author_sort | Maculins, Timurs |
collection | PubMed |
description | Ubiquitin signalling regulates most aspects of cellular life, thus deregulation of ubiquitylation has been linked with a number of diseases. E3 ubiquitin ligases provide substrate selectivity in ubiquitylation cascades and are therefore considered to be attractive targets for developing therapeutic molecules. In contrast to established drug target classes, such as protein kinases, GPCRs, hormone receptors and ion channels, ubiquitin drug discovery is in its early stages. This is, in part, due to the complexity of the ubiquitylation pathways and the lack of robust quantitative technologies that allow high-throughput screening of inhibitors. Here we report the development of a Ubiquitin Ligase Profiling system, which is a novel and generic cellular technology designed to facilitate identification of selective inhibitors against RING type E3 ubiquitin ligases. Utilization of this system requires a single co-transfection of cells with assay vectors, thereby enabling readout of E3 ubiquitin ligase catalytic activity within the cellular environment. Therefore, our robust high-throughput screening platform offers novel opportunities for the development of inhibitors against this difficult-to-target E3 ligase enzyme class. |
format | Online Article Text |
id | pubmed-4705515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47055152016-01-19 A Generic Platform for Cellular Screening Against Ubiquitin Ligases Maculins, Timurs Carter, Nikki Dorval, Thierry Hudson, Kevin Nissink, J. Willem M. Hay, Ronald T. Alwan, Husam Sci Rep Article Ubiquitin signalling regulates most aspects of cellular life, thus deregulation of ubiquitylation has been linked with a number of diseases. E3 ubiquitin ligases provide substrate selectivity in ubiquitylation cascades and are therefore considered to be attractive targets for developing therapeutic molecules. In contrast to established drug target classes, such as protein kinases, GPCRs, hormone receptors and ion channels, ubiquitin drug discovery is in its early stages. This is, in part, due to the complexity of the ubiquitylation pathways and the lack of robust quantitative technologies that allow high-throughput screening of inhibitors. Here we report the development of a Ubiquitin Ligase Profiling system, which is a novel and generic cellular technology designed to facilitate identification of selective inhibitors against RING type E3 ubiquitin ligases. Utilization of this system requires a single co-transfection of cells with assay vectors, thereby enabling readout of E3 ubiquitin ligase catalytic activity within the cellular environment. Therefore, our robust high-throughput screening platform offers novel opportunities for the development of inhibitors against this difficult-to-target E3 ligase enzyme class. Nature Publishing Group 2016-01-08 /pmc/articles/PMC4705515/ /pubmed/26743172 http://dx.doi.org/10.1038/srep18940 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Maculins, Timurs Carter, Nikki Dorval, Thierry Hudson, Kevin Nissink, J. Willem M. Hay, Ronald T. Alwan, Husam A Generic Platform for Cellular Screening Against Ubiquitin Ligases |
title | A Generic Platform for Cellular Screening Against Ubiquitin Ligases |
title_full | A Generic Platform for Cellular Screening Against Ubiquitin Ligases |
title_fullStr | A Generic Platform for Cellular Screening Against Ubiquitin Ligases |
title_full_unstemmed | A Generic Platform for Cellular Screening Against Ubiquitin Ligases |
title_short | A Generic Platform for Cellular Screening Against Ubiquitin Ligases |
title_sort | generic platform for cellular screening against ubiquitin ligases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705515/ https://www.ncbi.nlm.nih.gov/pubmed/26743172 http://dx.doi.org/10.1038/srep18940 |
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