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. 2012 May;81(5):419-29.
doi: 10.1002/cyto.a.22039. Epub 2012 Mar 21.

Cluster cytometry for high-capacity bioanalysis

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Cluster cytometry for high-capacity bioanalysis

Bruce S Edwards et al. Cytometry A. 2012 May.

Abstract

Flow cytometry specializes in high-content measurements of cells and particles in suspension. Having long excelled in analytical throughput of single cells and particles, only recently with the advent of HyperCyt sampling technology, flow cytometry's multiexperiment throughput has begun to approach the point of practicality for efficiently analyzing hundreds-of-thousands of samples, the realm of high-throughput screening (HTS). To extend performance and automation compatibility, we built a HyperCyt-linked Cluster Cytometer platform, a network of flow cytometers for analyzing samples displayed in high-density, 1,536-well plate format. To assess the performance, we used cell- and microsphere-based HTS assays that had been well characterized in the previous studies. Experiments addressed important technical issues: challenges of small wells (assay volumes 10 μL or less, reagent mixing, cell and particle suspension), detecting and correcting for differences in performance of individual flow cytometers, and the ability to reanalyze a plate in the event of problems encountered during the primary analysis. Boosting sample throughput an additional fourfold, this platform is uniquely positioned to synergize with expanding suspension array and cell barcoding technologies in which as many as 100 experiments are performed in a single well or sample. As high-performance flow cytometers shrink in cost and size, cluster cytometry promises to become a practical, productive approach for HTS, and other large-scale investigations of biological complexity.

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References

    1. Giuliano KA, DeBiasio RL, Dunlay RT, Gough A, Volosky JM, Zock J, Pavlakis G, Taylor DL. High-content screening: a new approach to easing key bottlenecks in the drug discovery process. J Biomol Screen. 1997;2:249–259.
    1. Haney SA, LaPan P, Pan J, Zhang J. High-content screening moves to the front of the line. Drug discovery today. 2006;11:889–94. - PubMed
    1. Kuckuck FW, Edwards BS, Sklar LA. High throughput flow cytometry. Cytometry. 2001;44:83–90. - PubMed
    1. Arterburn JB, Oprea TI, Prossnitz ER, Edwards BS, Sklar LA. Discovery of selective probes and antagonists for G-protein-coupled receptors FPR/FPRL1 and GPR30. Curr Top Med Chem. 2009;9:1227–36. - PMC - PubMed
    1. Sklar LA, Edwards BS. In: HTS flow cytometry, small molecule discovery, and the NIH Molecular Libraries Initative. Litvin V, Marder P, editors. Hoboken, NJ: John Wiley & Sons; 2010. pp. 71–98.

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