High-throughput flow cytometry-based assay to identify apoptosis-inducing proteins

J Biomol Screen. 2007 Jun;12(4):510-20. doi: 10.1177/1087057107301271. Epub 2007 May 3.

Abstract

After sequencing the human genome, the challenge ahead is to systematically analyze the functions and disease relation of the proteins encoded. Here the authors describe the application of a flow cytometry-based high-throughput assay to screen for apoptosis-activating proteins in transiently transfected cells. The assay is based on the detection of activated caspase-3 with a specific antibody, in cells overexpressing proteins tagged C- or N-terminally with yellow fluorescent protein. Fluorescence intensities are measured using a flow cytometer integrated with a high-throughput autosampler. The applicability of this screen has been tested in a pilot screen with 200 proteins. The candidate proteins were all verified in an independent microscopy-based nuclear fragmentation assay, finally resulting in the identification of 6 apoptosis inducers.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Apoptosis / physiology*
  • Apoptosis Regulatory Proteins / analysis*
  • Apoptosis Regulatory Proteins / biosynthesis*
  • Caspase 3 / analysis
  • Caspase 3 / biosynthesis
  • Cell Line
  • Flow Cytometry*
  • Humans
  • Pilot Projects

Substances

  • Apoptosis Regulatory Proteins
  • Caspase 3