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Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands

Antibodies raised against many cell surface proteins, including G protein-coupled receptors, remain important tools for their functional characterization. By linking antibodies to ligands for cell surface proteins, such adducts can be targeted to the surface of a cell type of choice. Site-specific f...

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Detalles Bibliográficos
Autores principales: Cheloha, Ross W., Fischer, Fabian A., Gardella, Thomas J., Ploegh, Hidde L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637866/
https://www.ncbi.nlm.nih.gov/pubmed/34977584
http://dx.doi.org/10.1039/d1cb00118c
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author Cheloha, Ross W.
Fischer, Fabian A.
Gardella, Thomas J.
Ploegh, Hidde L.
author_facet Cheloha, Ross W.
Fischer, Fabian A.
Gardella, Thomas J.
Ploegh, Hidde L.
author_sort Cheloha, Ross W.
collection PubMed
description Antibodies raised against many cell surface proteins, including G protein-coupled receptors, remain important tools for their functional characterization. By linking antibodies to ligands for cell surface proteins, such adducts can be targeted to the surface of a cell type of choice. Site-specific functionalization of full-size antibodies with synthetic moieties remains challenging. Here we present new approaches in which single domain antibodies (known as VHHs or nanobodies) that target either cell surface proteins or conventional antibodies are used to indirectly deliver ligands for GPCRs to their sites of action. The combination of high yield production of nanobodies, facile site-specific functionalization, and compatibility with commercially available mouse and rabbit antibodies should enable wide application of this approach.
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spelling pubmed-86378662021-12-30 Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands Cheloha, Ross W. Fischer, Fabian A. Gardella, Thomas J. Ploegh, Hidde L. RSC Chem Biol Chemistry Antibodies raised against many cell surface proteins, including G protein-coupled receptors, remain important tools for their functional characterization. By linking antibodies to ligands for cell surface proteins, such adducts can be targeted to the surface of a cell type of choice. Site-specific functionalization of full-size antibodies with synthetic moieties remains challenging. Here we present new approaches in which single domain antibodies (known as VHHs or nanobodies) that target either cell surface proteins or conventional antibodies are used to indirectly deliver ligands for GPCRs to their sites of action. The combination of high yield production of nanobodies, facile site-specific functionalization, and compatibility with commercially available mouse and rabbit antibodies should enable wide application of this approach. RSC 2021-10-11 /pmc/articles/PMC8637866/ /pubmed/34977584 http://dx.doi.org/10.1039/d1cb00118c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Cheloha, Ross W.
Fischer, Fabian A.
Gardella, Thomas J.
Ploegh, Hidde L.
Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands
title Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands
title_full Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands
title_fullStr Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands
title_full_unstemmed Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands
title_short Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands
title_sort activation of a g protein-coupled receptor through indirect antibody-mediated tethering of ligands
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637866/
https://www.ncbi.nlm.nih.gov/pubmed/34977584
http://dx.doi.org/10.1039/d1cb00118c
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