A validated antibody toolbox for ALS research
Riham Ayoubi, Emma J MacDougall, Ian McDowell, Michael S Biddle, Bárbara T Ferreira, CongYao Zha, Marie-France Dorion, Jay P Ross, Sara Gonzalez Bolivar, Vera Ruiz Moleon, Charles Alende, Vincent Francis, Maryam Fotouhi, Mathilde Chaineau, Carol X Chen, Valerio EC Piscopo, Vincent Soubannier, Irina Shlaifer, Zhipeng You, Michael Nicouleau, Tracy Keates, Wen Hwa Lee, Brian D Marsden, Leonidas Koukouflis, Edvard Wigren, Carolyn A Marks, Luke M Healy, Patrick A Dion, Guy A Rouleau, Edward A Fon, Harvinder S Virk, Susanne Gräslund, Opher Gileadi, Aled M Edwards, Thomas M Durcan, Peter S McPherson, Carl LaflammeA substantial fraction of amyotrophic lateral sclerosis (ALS)-associated proteins remains poorly characterized, in part because of the limited availability of validated research antibodies. We established knockout (KO)-based antibody characterization workflows and demonstrated that widely used antibodies against the major ALS-associated protein C9orf72 lacked specificity (Laflamme et al., 2019). We subsequently scaled this framework to systematically benchmark research antibodies, revealing that up to 61% fail to perform as recommended by manufacturers (Ayoubi et al., 2023b). Here, we extend this approach by establishing the ALS-Reproducible Antibody Platform (ALS-RAP), a comprehensive effort to generate a publicly available dataset of KO-validated antibodies targeting proteins encoded by ALS risk genes. In total, we characterized 303 antibodies against 33 ALS-associated proteins to identify high-quality reagents for use in western blot, immunoprecipitation, and immunofluorescence. Using these antibodies, we profiled protein levels across human induced pluripotent stem cell-derived and primary neurological cell types. These analyses revealed diverse cellular distributions and higher levels of several ALS-associated proteins in glial populations, consistent with emerging evidence for immune contributions to ALS. Together, ALS-RAP provides a validated antibody toolbox and protein expression resource to support the study of ALS-associated proteins.