The Heidelberg German Cancer Center research team integrated the Roche xCELLigence MP Instrument into a high-throughput workflow for assaying the effects of large numbers of different small interfering RNA (siRNA) transfections. They used a human siRNA library to perform a whole kinome screen, targeting 779 kinases and 80 cell cycle genes to analyze cell proliferation in real time, by monitoring the dynamics of the cellular responses after high-throughput gene knockdown. The team's findings showed that xCELLigence System measurements correlate with results obtained using, in parallel, conventional endpoint analyses, in particular Promega's CellTiter-Blue and Roche's WST-1 Cell Proliferation Reagent for assaying cell viability, as well as qRT-PCR for quantifying gene expression. However, the dynamic data obtained with the xCELLigence System allowed to identify the timing after transfection where the effect was maximal and to sort genes according to these time points.
"We have carried out a human kinome RNAi screen using xCELLigence with electrical impedance as output. This screen has confirmed previously identified inhibitor genes, as well as activators of cell proliferation. Our data establish the technology of the xCELLigence system as a novel tool amenable for high-throughput screening, opening new avenues in the dynamic cellular analysis of phenotypes induced by RNAi and other perturbations," summarizes Stefan Wiemann, one of the authors of the study and Head of the Division Molecular Genome Analysis at DKFZ.
The xCELLigence MP Instrument uses proprietary software and E-Plates 96 to measure electronic cell impedance using sensor electrodes. Computer-controlled signal generation and automatic frequency scanning, enable continual precise detection of changes in cell behavior using 96-well culture plates.