High-throughput flow cytometry for drug discovery

被引:27
作者
Edwards, Bruce S. [1 ]
Young, Susan M. [1 ]
Saunders, Matthew J. [2 ]
Bologa, Cristian [3 ]
Oprea, Tudor I. [3 ]
Ye, Richard D. [4 ]
Prossnitz, Eric R. [5 ]
Graves, Steven W. [2 ]
Sklar, Larry A. [1 ]
机构
[1] UNM HSC, CRTC, Cytometry & Dept Pathol, Albuquerque, NM 87131 USA
[2] Los Alamos Natl Lab, Natl Flow Cytometry Resource Biosci Div, Los Alamos, NM 87545 USA
[3] UNM HSC, Off Biocomp, Albuquerque, NM 87131 USA
[4] Univ Illinois, Dept Pharmacol, Chicago, IL 60612 USA
[5] UNM HSC, CRTC, Dept Cell Biol & Physiol, Albuquerque, NM 87131 USA
关键词
flow cytometry; fluorescence; formylpeptide receptor; formylpeptide receptor-like 1; high-content; high-throughput screening; Molecular Libraries Screening Network; NIH roadmap; protease;
D O I
10.1517/17460441.2.5.685
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
High-throughput flow cytometry exploits a novel many-samples/one-file approach to dramatically speed data acquisition, limit aspirated sample volume to as little as 2 mu l/well and produce multisample data sets that facilitate automated analysis of samples in groups as well as individually. It has been successfully applied to both cell- and microsphere-based bioassays in 96- and 384-well formats, to screen tens-of-thousands of compounds and identify novel bioactive structures. High-content multiparametric analysis capabilities have been exploited for assay multiplexing, allowing the assessment of biologic selectivity and specificity to be an integral component of primary screens. These and other advances in the last decade have contributed to the application of flow cytometry as a uniquely powerful tool for probing biologic and chemical diversity and complex systems biology.
引用
收藏
页码:685 / 696
页数:12
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