Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31612854.
- Also identified by DOI 10.7554/eLife.48363 and PMC identifier 6794092.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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 <i>C9ORF72</i> 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.
Medical subject headings
- Amyotrophic Lateral Sclerosis
- Antibodies, Monoclonal
- C9orf72 Protein
- Frontotemporal Dementia
- Immunohistochemistry