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Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72
Antibodies are a key resource in biomedical research yet there are no community-accepted standards to rigorously characterize their quality. Here we develop a procedure to validate pre-existing antibodies. Human cell lines with high expression of a target, determined through a proteomics database, a...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794092/ https://www.ncbi.nlm.nih.gov/pubmed/31612854 http://dx.doi.org/10.7554/eLife.48363 |
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author | Laflamme, Carl McKeever, Paul M Kumar, Rahul Schwartz, Julie Kolahdouzan, Mahshad Chen, Carol X You, Zhipeng Benaliouad, Faiza Gileadi, Opher McBride, Heidi M Durcan, Thomas M Edwards, Aled M Healy, Luke M Robertson, Janice McPherson, Peter S |
author_facet | Laflamme, Carl McKeever, Paul M Kumar, Rahul Schwartz, Julie Kolahdouzan, Mahshad Chen, Carol X You, Zhipeng Benaliouad, Faiza Gileadi, Opher McBride, Heidi M Durcan, Thomas M Edwards, Aled M Healy, Luke M Robertson, Janice McPherson, Peter S |
author_sort | Laflamme, Carl |
collection | PubMed |
description | Antibodies are a key resource in biomedical research yet there are no community-accepted standards to rigorously characterize their quality. Here we develop a procedure to validate pre-existing antibodies. Human cell lines with high expression of a target, determined through a proteomics database, are modified with CRISPR/Cas9 to knockout (KO) the corresponding gene. Commercial antibodies against the target are purchased and tested by immunoblot comparing parental and KO. Validated antibodies are used to definitively identify the most highly expressing cell lines, new KOs are generated if needed, and the lines are screened by immunoprecipitation and immunofluorescence. Selected antibodies are used for more intensive procedures such as immunohistochemistry. The pipeline is easy to implement and scalable. Application to the major ALS disease gene C9ORF72 identified high-quality antibodies revealing C9ORF72 localization to phagosomes/lysosomes. Antibodies that do not recognize C9ORF72 have been used in highly cited papers, raising concern over previously reported C9ORF72 properties. |
format | Online Article Text |
id | pubmed-6794092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67940922019-10-17 Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 Laflamme, Carl McKeever, Paul M Kumar, Rahul Schwartz, Julie Kolahdouzan, Mahshad Chen, Carol X You, Zhipeng Benaliouad, Faiza Gileadi, Opher McBride, Heidi M Durcan, Thomas M Edwards, Aled M Healy, Luke M Robertson, Janice McPherson, Peter S eLife Cell Biology Antibodies are a key resource in biomedical research yet there are no community-accepted standards to rigorously characterize their quality. Here we develop a procedure to validate pre-existing antibodies. Human cell lines with high expression of a target, determined through a proteomics database, are modified with CRISPR/Cas9 to knockout (KO) the corresponding gene. Commercial antibodies against the target are purchased and tested by immunoblot comparing parental and KO. Validated antibodies are used to definitively identify the most highly expressing cell lines, new KOs are generated if needed, and the lines are screened by immunoprecipitation and immunofluorescence. Selected antibodies are used for more intensive procedures such as immunohistochemistry. The pipeline is easy to implement and scalable. Application to the major ALS disease gene C9ORF72 identified high-quality antibodies revealing C9ORF72 localization to phagosomes/lysosomes. Antibodies that do not recognize C9ORF72 have been used in highly cited papers, raising concern over previously reported C9ORF72 properties. eLife Sciences Publications, Ltd 2019-10-15 /pmc/articles/PMC6794092/ /pubmed/31612854 http://dx.doi.org/10.7554/eLife.48363 Text en © 2019, Laflamme et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Laflamme, Carl McKeever, Paul M Kumar, Rahul Schwartz, Julie Kolahdouzan, Mahshad Chen, Carol X You, Zhipeng Benaliouad, Faiza Gileadi, Opher McBride, Heidi M Durcan, Thomas M Edwards, Aled M Healy, Luke M Robertson, Janice McPherson, Peter S Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 |
title | Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 |
title_full | Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 |
title_fullStr | Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 |
title_full_unstemmed | Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 |
title_short | Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72 |
title_sort | implementation of an antibody characterization procedure and application to the major als/ftd disease gene c9orf72 |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794092/ https://www.ncbi.nlm.nih.gov/pubmed/31612854 http://dx.doi.org/10.7554/eLife.48363 |
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