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Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay
The discovery of potent cell-permeable E3 ubiquitin ligase ligands can significantly facilitate the development of proteolysis targeting chimeras (PROTACs). Here, we present a protocol to determine the binding affinity of ligands toward CRBN E3 ubiquitin ligase, using a cellular target engagement me...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829257/ https://www.ncbi.nlm.nih.gov/pubmed/33532735 http://dx.doi.org/10.1016/j.xpro.2020.100288 |
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author | Yang, Ka Zhou, Yaxian Roberts, Brett L. Nie, Xueqing Tang, Weiping |
author_facet | Yang, Ka Zhou, Yaxian Roberts, Brett L. Nie, Xueqing Tang, Weiping |
author_sort | Yang, Ka |
collection | PubMed |
description | The discovery of potent cell-permeable E3 ubiquitin ligase ligands can significantly facilitate the development of proteolysis targeting chimeras (PROTACs). Here, we present a protocol to determine the binding affinity of ligands toward CRBN E3 ubiquitin ligase, using a cellular target engagement mechanism and in-cell ELISA assay. This protocol is easy to establish, with relatively low cost and rapid time frame. It can also be modified to measure the level of other proteins or determine the ligand affinity toward other E3s. For complete details on the use and execution of this protocol, please refer to Yang et al. (2020). |
format | Online Article Text |
id | pubmed-7829257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78292572021-02-01 Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay Yang, Ka Zhou, Yaxian Roberts, Brett L. Nie, Xueqing Tang, Weiping STAR Protoc Protocol The discovery of potent cell-permeable E3 ubiquitin ligase ligands can significantly facilitate the development of proteolysis targeting chimeras (PROTACs). Here, we present a protocol to determine the binding affinity of ligands toward CRBN E3 ubiquitin ligase, using a cellular target engagement mechanism and in-cell ELISA assay. This protocol is easy to establish, with relatively low cost and rapid time frame. It can also be modified to measure the level of other proteins or determine the ligand affinity toward other E3s. For complete details on the use and execution of this protocol, please refer to Yang et al. (2020). Elsevier 2021-01-22 /pmc/articles/PMC7829257/ /pubmed/33532735 http://dx.doi.org/10.1016/j.xpro.2020.100288 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Yang, Ka Zhou, Yaxian Roberts, Brett L. Nie, Xueqing Tang, Weiping Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay |
title | Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay |
title_full | Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay |
title_fullStr | Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay |
title_full_unstemmed | Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay |
title_short | Evaluation of the binding affinity of E3 ubiquitin ligase ligands by cellular target engagement and in-cell ELISA assay |
title_sort | evaluation of the binding affinity of e3 ubiquitin ligase ligands by cellular target engagement and in-cell elisa assay |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829257/ https://www.ncbi.nlm.nih.gov/pubmed/33532735 http://dx.doi.org/10.1016/j.xpro.2020.100288 |
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