Author:
Chitale Shalaka,Wu Wenxuan,Mukherjee Avik,Lannon Herbert,Suresh Pooja,Nag Ishan,Ambrosi Christina M.,Gertner Rona S.,Melo Hendrick,Powers Brendan,Wilkins Hollin,Hinton Henry,Cheah Mickey,Boynton Zachariah,Alexeyev Alexander,Sword Duane,Basan Markus,Park Hongkun,Ham Donhee,Abbott Jeffrey
Abstract
AbstractProfiling compounds and genetic perturbations via high-content imaging has become increasingly popular for drug discovery, but the technique is limited to endpoint images of fixed cells. In contrast, electronic-based devices offer label-free, functional information of live cells, yet current approaches suffer from low-spatial resolution or single-well throughput. Here, we report a semiconductor 96-microplate platform designed for high-resolution real-time impedance “imaging” at scale. Each well features 4,096 electrodes at 25 µm spatial resolution while a miniaturized data interface allows 8× parallel plate operation (768 total wells) within each incubator for enhanced throughputs. New electric field-based, multi-frequency measurement techniques capture >20 parameter images including tissue barrier, cell-surface attachment, cell flatness, and motility every 15 min throughout experiments. Using these real-time readouts, we characterized 16 cell types, ranging from primary epithelial to suspension, and quantified heterogeneity in mixed epithelial and mesenchymal co-cultures. A proof-of-concept screen of 904 diverse compounds using 13 semiconductor microplates demonstrates the platform’s capability for mechanism of action (MOA) profiling with 25 distinct responses identified. The scalability of the semiconductor platform combined with the translatability of the high dimensional live-cell functional parameters expands high-throughput MOA profiling and phenotypic drug discovery applications.
Publisher
Cold Spring Harbor Laboratory