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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...

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Detalles Bibliográficos
Autores principales: Yang, Ka, Zhou, Yaxian, Roberts, Brett L., Nie, Xueqing, Tang, Weiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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).
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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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