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An Affinity-Based Probe for the Human Adenosine A(2A) Receptor
[Image: see text] Using activity-based protein profiling (ABPP), functional proteins can be interrogated in their native environment. Despite their pharmaceutical relevance, G protein-coupled receptors (GPCRs) have been difficult to address through ABPP. In the current study, we took the prototypica...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150691/ https://www.ncbi.nlm.nih.gov/pubmed/30080404 http://dx.doi.org/10.1021/acs.jmedchem.8b00860 |
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author | Yang, Xue Michiels, Thomas J. M. de Jong, Coen Soethoudt, Marjolein Dekker, Niek Gordon, Euan van der Stelt, Mario Heitman, Laura H. van der Es, Daan IJzerman, Adriaan P. |
author_facet | Yang, Xue Michiels, Thomas J. M. de Jong, Coen Soethoudt, Marjolein Dekker, Niek Gordon, Euan van der Stelt, Mario Heitman, Laura H. van der Es, Daan IJzerman, Adriaan P. |
author_sort | Yang, Xue |
collection | PubMed |
description | [Image: see text] Using activity-based protein profiling (ABPP), functional proteins can be interrogated in their native environment. Despite their pharmaceutical relevance, G protein-coupled receptors (GPCRs) have been difficult to address through ABPP. In the current study, we took the prototypical human adenosine A(2A) receptor (hA(2A)R) as the starting point for the construction of a chemical toolbox allowing two-step affinity-based labeling of GPCRs. First, we equipped an irreversibly binding hA(2A)R ligand with a terminal alkyne to serve as probe. We showed that our probe irreversibly and concentration-dependently labeled purified hA(2A)R. Click-ligation with a sulfonated cyanine-3 fluorophore allowed us to visualize the receptor on SDS-PAGE. We further demonstrated that labeling of the purified hA(2A)R by our probe could be inhibited by selective antagonists. Lastly, we showed successful labeling of the receptor in cell membranes overexpressing hA(2A)R, making our probe a promising affinity-based tool compound that sets the stage for the further development of probes for GPCRs. |
format | Online Article Text |
id | pubmed-6150691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61506912018-09-24 An Affinity-Based Probe for the Human Adenosine A(2A) Receptor Yang, Xue Michiels, Thomas J. M. de Jong, Coen Soethoudt, Marjolein Dekker, Niek Gordon, Euan van der Stelt, Mario Heitman, Laura H. van der Es, Daan IJzerman, Adriaan P. J Med Chem [Image: see text] Using activity-based protein profiling (ABPP), functional proteins can be interrogated in their native environment. Despite their pharmaceutical relevance, G protein-coupled receptors (GPCRs) have been difficult to address through ABPP. In the current study, we took the prototypical human adenosine A(2A) receptor (hA(2A)R) as the starting point for the construction of a chemical toolbox allowing two-step affinity-based labeling of GPCRs. First, we equipped an irreversibly binding hA(2A)R ligand with a terminal alkyne to serve as probe. We showed that our probe irreversibly and concentration-dependently labeled purified hA(2A)R. Click-ligation with a sulfonated cyanine-3 fluorophore allowed us to visualize the receptor on SDS-PAGE. We further demonstrated that labeling of the purified hA(2A)R by our probe could be inhibited by selective antagonists. Lastly, we showed successful labeling of the receptor in cell membranes overexpressing hA(2A)R, making our probe a promising affinity-based tool compound that sets the stage for the further development of probes for GPCRs. American Chemical Society 2018-08-06 2018-09-13 /pmc/articles/PMC6150691/ /pubmed/30080404 http://dx.doi.org/10.1021/acs.jmedchem.8b00860 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Yang, Xue Michiels, Thomas J. M. de Jong, Coen Soethoudt, Marjolein Dekker, Niek Gordon, Euan van der Stelt, Mario Heitman, Laura H. van der Es, Daan IJzerman, Adriaan P. An Affinity-Based Probe for the Human Adenosine A(2A) Receptor |
title | An Affinity-Based
Probe for the Human Adenosine A(2A) Receptor |
title_full | An Affinity-Based
Probe for the Human Adenosine A(2A) Receptor |
title_fullStr | An Affinity-Based
Probe for the Human Adenosine A(2A) Receptor |
title_full_unstemmed | An Affinity-Based
Probe for the Human Adenosine A(2A) Receptor |
title_short | An Affinity-Based
Probe for the Human Adenosine A(2A) Receptor |
title_sort | affinity-based
probe for the human adenosine a(2a) receptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150691/ https://www.ncbi.nlm.nih.gov/pubmed/30080404 http://dx.doi.org/10.1021/acs.jmedchem.8b00860 |
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