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Highly sensitive detection of antibody nonspecific interactions using flow cytometry

The rapidly evolving nature of antibody drug development has resulted in technologies that generate vast numbers (hundreds to thousands) of lead antibody candidates during early discovery. These candidates must be rapidly pared down to identify the most drug-like candidates for in-depth analysis of...

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Autores principales: Makowski, Emily K., Wu, Lina, Desai, Alec A., Tessier, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317921/
https://www.ncbi.nlm.nih.gov/pubmed/34313552
http://dx.doi.org/10.1080/19420862.2021.1951426
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author Makowski, Emily K.
Wu, Lina
Desai, Alec A.
Tessier, Peter M.
author_facet Makowski, Emily K.
Wu, Lina
Desai, Alec A.
Tessier, Peter M.
author_sort Makowski, Emily K.
collection PubMed
description The rapidly evolving nature of antibody drug development has resulted in technologies that generate vast numbers (hundreds to thousands) of lead antibody candidates during early discovery. These candidates must be rapidly pared down to identify the most drug-like candidates for in-depth analysis of their safety and efficacy, which can only be performed on a limited number of antibodies due to time and resource requirements. One key biophysical property of successful antibody therapeutics is high specificity, defined as low levels of nonspecific binding or polyspecificity. Although there has been some progress in developing assays for detecting antibody polyspecificity, most of these assays are limited by poor sensitivity or assay formats that require proprietary antibody surface display methods, and some of these assays use complex and poorly defined polyspecificity reagents. Here we report the PolySpecificity Particle (PSP) assay, a sensitive flow cytometry assay for evaluating antibody nonspecific interactions that overcomes previous limitations and can be used for evaluating diverse types of IgGs, multispecific antibodies and Fc-fusion proteins. Our approach uses micron-sized magnetic beads coated with Protein A to capture antibodies at extremely dilute concentrations (<0.02 mg/mL). Flow cytometry analysis of polyspecificity reagent binding to these conjugates results in sensitive detection of differences in nonspecific interactions for clinical-stage antibodies. Our PSP assay strongly discriminates between antibodies with different levels of polyspecificity using previously reported polyspecificity reagents that are either well-defined proteins or highly complex protein mixtures. Moreover, we also find that a unique reagent, namely ovalbumin, results in the best assay sensitivity and specificity. Importantly, our assay is much more sensitive than standard assays such as ELISAs. We expect that our simple, sensitive, and high-throughput PSP assay will accelerate the development of safe and effective antibody therapeutics.
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spelling pubmed-83179212021-08-06 Highly sensitive detection of antibody nonspecific interactions using flow cytometry Makowski, Emily K. Wu, Lina Desai, Alec A. Tessier, Peter M. MAbs Report The rapidly evolving nature of antibody drug development has resulted in technologies that generate vast numbers (hundreds to thousands) of lead antibody candidates during early discovery. These candidates must be rapidly pared down to identify the most drug-like candidates for in-depth analysis of their safety and efficacy, which can only be performed on a limited number of antibodies due to time and resource requirements. One key biophysical property of successful antibody therapeutics is high specificity, defined as low levels of nonspecific binding or polyspecificity. Although there has been some progress in developing assays for detecting antibody polyspecificity, most of these assays are limited by poor sensitivity or assay formats that require proprietary antibody surface display methods, and some of these assays use complex and poorly defined polyspecificity reagents. Here we report the PolySpecificity Particle (PSP) assay, a sensitive flow cytometry assay for evaluating antibody nonspecific interactions that overcomes previous limitations and can be used for evaluating diverse types of IgGs, multispecific antibodies and Fc-fusion proteins. Our approach uses micron-sized magnetic beads coated with Protein A to capture antibodies at extremely dilute concentrations (<0.02 mg/mL). Flow cytometry analysis of polyspecificity reagent binding to these conjugates results in sensitive detection of differences in nonspecific interactions for clinical-stage antibodies. Our PSP assay strongly discriminates between antibodies with different levels of polyspecificity using previously reported polyspecificity reagents that are either well-defined proteins or highly complex protein mixtures. Moreover, we also find that a unique reagent, namely ovalbumin, results in the best assay sensitivity and specificity. Importantly, our assay is much more sensitive than standard assays such as ELISAs. We expect that our simple, sensitive, and high-throughput PSP assay will accelerate the development of safe and effective antibody therapeutics. Taylor & Francis 2021-07-27 /pmc/articles/PMC8317921/ /pubmed/34313552 http://dx.doi.org/10.1080/19420862.2021.1951426 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Report
Makowski, Emily K.
Wu, Lina
Desai, Alec A.
Tessier, Peter M.
Highly sensitive detection of antibody nonspecific interactions using flow cytometry
title Highly sensitive detection of antibody nonspecific interactions using flow cytometry
title_full Highly sensitive detection of antibody nonspecific interactions using flow cytometry
title_fullStr Highly sensitive detection of antibody nonspecific interactions using flow cytometry
title_full_unstemmed Highly sensitive detection of antibody nonspecific interactions using flow cytometry
title_short Highly sensitive detection of antibody nonspecific interactions using flow cytometry
title_sort highly sensitive detection of antibody nonspecific interactions using flow cytometry
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317921/
https://www.ncbi.nlm.nih.gov/pubmed/34313552
http://dx.doi.org/10.1080/19420862.2021.1951426
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