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Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies

G-protein-coupled receptors (GPCR) transmit extracellular signals into cells to regulate a variety of cellular functions and are closely related to the homeostasis of the human body and the progression of various types of diseases. Great attention has been paid to GPCRs as excellent drug targets, an...

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Autores principales: Ju, Man-Seok, Jung, Sang Taek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663707/
https://www.ncbi.nlm.nih.gov/pubmed/33153215
http://dx.doi.org/10.3390/ijms21218240
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author Ju, Man-Seok
Jung, Sang Taek
author_facet Ju, Man-Seok
Jung, Sang Taek
author_sort Ju, Man-Seok
collection PubMed
description G-protein-coupled receptors (GPCR) transmit extracellular signals into cells to regulate a variety of cellular functions and are closely related to the homeostasis of the human body and the progression of various types of diseases. Great attention has been paid to GPCRs as excellent drug targets, and there are many commercially available small-molecule chemical drugs against GPCRs. Despite this, the development of therapeutic anti-GPCR antibodies has been delayed and is challenging due to the difficulty in preparing active forms of GPCR antigens, resulting from their low cellular expression and complex structures. Here, we focus on anti-GPCR antibodies that have been approved or are subject to clinical trials and present various technologies to prepare active GPCR antigens that enable the isolation of therapeutic antibodies to proceed toward clinical validation.
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spelling pubmed-76637072020-11-14 Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies Ju, Man-Seok Jung, Sang Taek Int J Mol Sci Review G-protein-coupled receptors (GPCR) transmit extracellular signals into cells to regulate a variety of cellular functions and are closely related to the homeostasis of the human body and the progression of various types of diseases. Great attention has been paid to GPCRs as excellent drug targets, and there are many commercially available small-molecule chemical drugs against GPCRs. Despite this, the development of therapeutic anti-GPCR antibodies has been delayed and is challenging due to the difficulty in preparing active forms of GPCR antigens, resulting from their low cellular expression and complex structures. Here, we focus on anti-GPCR antibodies that have been approved or are subject to clinical trials and present various technologies to prepare active GPCR antigens that enable the isolation of therapeutic antibodies to proceed toward clinical validation. MDPI 2020-11-03 /pmc/articles/PMC7663707/ /pubmed/33153215 http://dx.doi.org/10.3390/ijms21218240 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ju, Man-Seok
Jung, Sang Taek
Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies
title Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies
title_full Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies
title_fullStr Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies
title_full_unstemmed Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies
title_short Antigen Design for Successful Isolation of Highly Challenging Therapeutic Anti-GPCR Antibodies
title_sort antigen design for successful isolation of highly challenging therapeutic anti-gpcr antibodies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663707/
https://www.ncbi.nlm.nih.gov/pubmed/33153215
http://dx.doi.org/10.3390/ijms21218240
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