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A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations
Cell surface antigen discovery is of great interest for biomedical research both for isolation of rare cell populations and therapeutic targeting. We developed a rapid, cost-effective, fully in vitro technology which facilities the simultaneous target discovery and human antibody generation on the s...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351593/ https://www.ncbi.nlm.nih.gov/pubmed/30696911 http://dx.doi.org/10.1038/s41598-018-37462-1 |
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author | Nixon, Allison M. L. Duque, Alejandro Yelle, Nicholas McLaughlin, Megan Davoudi, Sadegh Pedley, Nicolas M. Haynes, Jennifer Brown, Kevin R. Pan, James Hart, Traver Gilbert, Penney M. Singh, Sheila K. O’Brien, Catherine A. Sidhu, Sachdev S. Moffat, Jason |
author_facet | Nixon, Allison M. L. Duque, Alejandro Yelle, Nicholas McLaughlin, Megan Davoudi, Sadegh Pedley, Nicolas M. Haynes, Jennifer Brown, Kevin R. Pan, James Hart, Traver Gilbert, Penney M. Singh, Sheila K. O’Brien, Catherine A. Sidhu, Sachdev S. Moffat, Jason |
author_sort | Nixon, Allison M. L. |
collection | PubMed |
description | Cell surface antigen discovery is of great interest for biomedical research both for isolation of rare cell populations and therapeutic targeting. We developed a rapid, cost-effective, fully in vitro technology which facilities the simultaneous target discovery and human antibody generation on the surface of virtually any cell population of interest. We apply our technique to human colorectal cancer-initiating cells (CICs) and identify hundreds of unique human antibodies. We characterized the top three antibody candidates targeting these CICs and identify their protein targets as integrin α7 (ITGA7), HLA-A1 and integrin β6 (ITGB6). We demonstrate that these antibodies can be used to isolate self-renewing colorectal CICs, and that the integrin α7 antibody can prospectively identify glioblastoma brain tumor initiating cells as well as human muscle stem cells. We also demonstrate that genetic ablation of integrin β6 impedes colorectal CIC function. The methodology can be readily applied to other cell populations including stem cells, cancer, or immune cells to facilitate the rapid identification of novel targets and simultaneous generation of potent and specific antibodies with therapeutic potential. |
format | Online Article Text |
id | pubmed-6351593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63515932019-01-31 A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations Nixon, Allison M. L. Duque, Alejandro Yelle, Nicholas McLaughlin, Megan Davoudi, Sadegh Pedley, Nicolas M. Haynes, Jennifer Brown, Kevin R. Pan, James Hart, Traver Gilbert, Penney M. Singh, Sheila K. O’Brien, Catherine A. Sidhu, Sachdev S. Moffat, Jason Sci Rep Article Cell surface antigen discovery is of great interest for biomedical research both for isolation of rare cell populations and therapeutic targeting. We developed a rapid, cost-effective, fully in vitro technology which facilities the simultaneous target discovery and human antibody generation on the surface of virtually any cell population of interest. We apply our technique to human colorectal cancer-initiating cells (CICs) and identify hundreds of unique human antibodies. We characterized the top three antibody candidates targeting these CICs and identify their protein targets as integrin α7 (ITGA7), HLA-A1 and integrin β6 (ITGB6). We demonstrate that these antibodies can be used to isolate self-renewing colorectal CICs, and that the integrin α7 antibody can prospectively identify glioblastoma brain tumor initiating cells as well as human muscle stem cells. We also demonstrate that genetic ablation of integrin β6 impedes colorectal CIC function. The methodology can be readily applied to other cell populations including stem cells, cancer, or immune cells to facilitate the rapid identification of novel targets and simultaneous generation of potent and specific antibodies with therapeutic potential. Nature Publishing Group UK 2019-01-29 /pmc/articles/PMC6351593/ /pubmed/30696911 http://dx.doi.org/10.1038/s41598-018-37462-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nixon, Allison M. L. Duque, Alejandro Yelle, Nicholas McLaughlin, Megan Davoudi, Sadegh Pedley, Nicolas M. Haynes, Jennifer Brown, Kevin R. Pan, James Hart, Traver Gilbert, Penney M. Singh, Sheila K. O’Brien, Catherine A. Sidhu, Sachdev S. Moffat, Jason A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
title | A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
title_full | A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
title_fullStr | A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
title_full_unstemmed | A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
title_short | A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
title_sort | rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351593/ https://www.ncbi.nlm.nih.gov/pubmed/30696911 http://dx.doi.org/10.1038/s41598-018-37462-1 |
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