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Versatile and rapid microfluidics-assisted antibody discovery
Recent years have seen unparalleled development of microfluidic applications for antibody discovery in both academic and pharmaceutical research. Microfluidics can support native chain-paired library generation as well as direct screening of antibody secreting cells obtained by rodent immunization o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489958/ https://www.ncbi.nlm.nih.gov/pubmed/34586015 http://dx.doi.org/10.1080/19420862.2021.1978130 |
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author | Gaa, Ramona Menang-Ndi, Emmanuel Pratapa, Shruti Nguyen, Christine Kumar, Satyendra Doerner, Achim |
author_facet | Gaa, Ramona Menang-Ndi, Emmanuel Pratapa, Shruti Nguyen, Christine Kumar, Satyendra Doerner, Achim |
author_sort | Gaa, Ramona |
collection | PubMed |
description | Recent years have seen unparalleled development of microfluidic applications for antibody discovery in both academic and pharmaceutical research. Microfluidics can support native chain-paired library generation as well as direct screening of antibody secreting cells obtained by rodent immunization or from the human peripheral blood. While broad diversities of neutralizing antibodies against infectious diseases such as HIV, Ebola, or COVID-19 have been identified from convalescent individuals, microfluidics can expedite therapeutic antibody discovery for cancer or immunological disease indications. In this study, a commercially available microfluidic device, Cyto-Mine, was used for the rapid identification of natively paired antibodies from rodents or human donors screened for specific binding to recombinant antigens, for direct screening with cells expressing the target of interest, and, to our knowledge for the first time, for direct broad functional IgG antibody screening in droplets. The process time from cell preparation to confirmed recombinant antibodies was four weeks. Application of this or similar microfluidic devices and methodologies can accelerate and enhance pharmaceutical antibody hit discovery. |
format | Online Article Text |
id | pubmed-8489958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84899582021-10-05 Versatile and rapid microfluidics-assisted antibody discovery Gaa, Ramona Menang-Ndi, Emmanuel Pratapa, Shruti Nguyen, Christine Kumar, Satyendra Doerner, Achim MAbs Report Recent years have seen unparalleled development of microfluidic applications for antibody discovery in both academic and pharmaceutical research. Microfluidics can support native chain-paired library generation as well as direct screening of antibody secreting cells obtained by rodent immunization or from the human peripheral blood. While broad diversities of neutralizing antibodies against infectious diseases such as HIV, Ebola, or COVID-19 have been identified from convalescent individuals, microfluidics can expedite therapeutic antibody discovery for cancer or immunological disease indications. In this study, a commercially available microfluidic device, Cyto-Mine, was used for the rapid identification of natively paired antibodies from rodents or human donors screened for specific binding to recombinant antigens, for direct screening with cells expressing the target of interest, and, to our knowledge for the first time, for direct broad functional IgG antibody screening in droplets. The process time from cell preparation to confirmed recombinant antibodies was four weeks. Application of this or similar microfluidic devices and methodologies can accelerate and enhance pharmaceutical antibody hit discovery. Taylor & Francis 2021-09-29 /pmc/articles/PMC8489958/ /pubmed/34586015 http://dx.doi.org/10.1080/19420862.2021.1978130 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 Gaa, Ramona Menang-Ndi, Emmanuel Pratapa, Shruti Nguyen, Christine Kumar, Satyendra Doerner, Achim Versatile and rapid microfluidics-assisted antibody discovery |
title | Versatile and rapid microfluidics-assisted antibody discovery |
title_full | Versatile and rapid microfluidics-assisted antibody discovery |
title_fullStr | Versatile and rapid microfluidics-assisted antibody discovery |
title_full_unstemmed | Versatile and rapid microfluidics-assisted antibody discovery |
title_short | Versatile and rapid microfluidics-assisted antibody discovery |
title_sort | versatile and rapid microfluidics-assisted antibody discovery |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489958/ https://www.ncbi.nlm.nih.gov/pubmed/34586015 http://dx.doi.org/10.1080/19420862.2021.1978130 |
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