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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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.
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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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