Gustafsdottir SM, Ljosa V, Sokolnicki KL, Anthony Wilson J, Walpita D, Kemp MM, Petri Seiler K, Carrel HA, Golub TR, Schreiber SL, et al. Multiplex cytological profiling assay to measure diverse cellular states. PLoS One. 2013;8:e80999.
NOTES
Gustafsdottir, Sigrun MLjosa, VebjornSokolnicki, Katherine LAnthony Wilson, JWalpita, DeepikaKemp, Melissa MPetri Seiler, KathleenCarrel, Hyman AGolub, Todd RSchreiber, Stuart LClemons, Paul ACarpenter, Anne EShamji, Alykhan FengRL1HG004671/HG/NHGRI NIH HHS/U54 HG005032/HG/NHGRI NIH HHS/UL1 RR024924/RR/NCRR NIH HHS/RL1 GM084437/GM/NIGMS NIH HHS/RL1 HG004671/HG/NHGRI NIH HHS/RL1 CA133834/CA/NCI NIH HHS/Research Support, N.I.H., ExtramuralResearch Support, U.S. Gov't, Non-P.H.S.PLoS One. 2013 Dec 2;8(12):e80999. doi: 10.1371/journal.pone.0080999. eCollection 2013.
Abstract
Computational methods for image-based profiling are under active development, but their success hinges on assays that can capture a wide range of phenotypes. We have developed a multiplex cytological profiling assay that "paints the cell" with as many fluorescent markers as possible without compromising our ability to extract rich, quantitative profiles in high throughput. The assay detects seven major cellular components. In a pilot screen of bioactive compounds, the assay detected a range of cellular phenotypes and it clustered compounds with similar annotated protein targets or chemical structure based on cytological profiles. The results demonstrate that the assay captures subtle patterns in the combination of morphological labels, thereby detecting the effects of chemical compounds even though their targets are not stained directly. This image-based assay provides an unbiased approach to characterize compound- and disease-associated cell states to support future probe discovery.
Last updated on 02/17/2021