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Engineering therapeutic antibodies targeting G-protein–coupled receptors

G-protein–coupled receptors (GPCRs) are one of the most attractive therapeutic target classes because of their critical roles in intracellular signaling and their clinical relevance to a variety of diseases, including cancer, infection and inflammation. However, high conformational variability, the...

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Detalles Bibliográficos
Autores principales: Jo, Migyeong, Jung, Sang Taek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892866/
https://www.ncbi.nlm.nih.gov/pubmed/26846450
http://dx.doi.org/10.1038/emm.2015.105
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author Jo, Migyeong
Jung, Sang Taek
author_facet Jo, Migyeong
Jung, Sang Taek
author_sort Jo, Migyeong
collection PubMed
description G-protein–coupled receptors (GPCRs) are one of the most attractive therapeutic target classes because of their critical roles in intracellular signaling and their clinical relevance to a variety of diseases, including cancer, infection and inflammation. However, high conformational variability, the small exposed area of extracellular epitopes and difficulty in the preparation of GPCR antigens have delayed both the isolation of therapeutic anti-GPCR antibodies as well as studies on the structure, function and biochemical mechanisms of GPCRs. To overcome the challenges in generating highly specific anti-GPCR antibodies with enhanced efficacy and safety, various forms of antigens have been successfully designed and employed for screening with newly emerged systems based on laboratory animal immunization and high-throughput-directed evolution.
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spelling pubmed-48928662016-07-27 Engineering therapeutic antibodies targeting G-protein–coupled receptors Jo, Migyeong Jung, Sang Taek Exp Mol Med Review G-protein–coupled receptors (GPCRs) are one of the most attractive therapeutic target classes because of their critical roles in intracellular signaling and their clinical relevance to a variety of diseases, including cancer, infection and inflammation. However, high conformational variability, the small exposed area of extracellular epitopes and difficulty in the preparation of GPCR antigens have delayed both the isolation of therapeutic anti-GPCR antibodies as well as studies on the structure, function and biochemical mechanisms of GPCRs. To overcome the challenges in generating highly specific anti-GPCR antibodies with enhanced efficacy and safety, various forms of antigens have been successfully designed and employed for screening with newly emerged systems based on laboratory animal immunization and high-throughput-directed evolution. Nature Publishing Group 2016-02 2016-02-05 /pmc/articles/PMC4892866/ /pubmed/26846450 http://dx.doi.org/10.1038/emm.2015.105 Text en Copyright © 2016 KSBMB. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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-nc-nd/4.0/
spellingShingle Review
Jo, Migyeong
Jung, Sang Taek
Engineering therapeutic antibodies targeting G-protein–coupled receptors
title Engineering therapeutic antibodies targeting G-protein–coupled receptors
title_full Engineering therapeutic antibodies targeting G-protein–coupled receptors
title_fullStr Engineering therapeutic antibodies targeting G-protein–coupled receptors
title_full_unstemmed Engineering therapeutic antibodies targeting G-protein–coupled receptors
title_short Engineering therapeutic antibodies targeting G-protein–coupled receptors
title_sort engineering therapeutic antibodies targeting g-protein–coupled receptors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892866/
https://www.ncbi.nlm.nih.gov/pubmed/26846450
http://dx.doi.org/10.1038/emm.2015.105
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