A Fully Automated High-Throughput Flow Cytometry Screening System Enabling Phenotypic Drug Discovery

Author:

Joslin John1,Gilligan James1,Anderson Paul1,Garcia Catherine1,Sharif Orzala1,Hampton Janice1,Cohen Steven1,King Miranda1,Zhou Bin1,Jiang Shumei1,Trussell Christopher1,Dunn Robert1,Fathman John W.1,Snead Jennifer L.1,Boitano Anthony E.1,Nguyen Tommy1,Conner Michael1,Cooke Mike1,Harris Jennifer1,Ainscow Ed1,Zhou Yingyao1,Shaw Chris1,Sipes Dan1,Mainquist James1,Lesley Scott1

Affiliation:

1. Genomics Institute of the Novartis Research Foundation, San Diego, CA, USA

Abstract

The goal of high-throughput screening is to enable screening of compound libraries in an automated manner to identify quality starting points for optimization. This often involves screening a large diversity of compounds in an assay that preserves a connection to the disease pathology. Phenotypic screening is a powerful tool for drug identification, in that assays can be run without prior understanding of the target and with primary cells that closely mimic the therapeutic setting. Advanced automation and high-content imaging have enabled many complex assays, but these are still relatively slow and low throughput. To address this limitation, we have developed an automated workflow that is dedicated to processing complex phenotypic assays for flow cytometry. The system can achieve a throughput of 50,000 wells per day, resulting in a fully automated platform that enables robust phenotypic drug discovery. Over the past 5 years, this screening system has been used for a variety of drug discovery programs, across many disease areas, with many molecules advancing quickly into preclinical development and into the clinic. This report will highlight a diversity of approaches that automated flow cytometry has enabled for phenotypic drug discovery.

Publisher

Elsevier BV

Subject

Molecular Medicine,Biochemistry,Analytical Chemistry,Biotechnology

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