Characterization of Cellular Viability Using Label-Free Brightfield Live-Cell Imaging

Methods Mol Biol. 2023:2706:75-88. doi: 10.1007/978-1-0716-3397-7_6.

Abstract

In recent years, the assembly and annotation of chemogenomic libraries have gained interest by the phenotypic screening community. Apart from basic annotations of the compound potency and selectivity, these compound libraries benefit in particular from annotation regarding the effect of the inhibitors on cellular viability to distinguish between on-target effects of a compound and unspecific cytotoxicity. Here, we provide a protocol to determine viability as a first determinant in compound quality control, using the Incucyte live-cell imaging system. The compounds are classified according to their calculated growth rate to determine a cytotoxic, cytostatic, or healthy outcome. All compounds affecting the growth rate can be further evaluated regarding their specific effects on cell health in a high-content live-cell multiplex assay, described in Chapter 5 .

Keywords: Cytotoxicity; Growth rate; Phenotypic screening; Viability assay.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival*
  • Microscopy* / methods