A low-volume platform for cell-respirometric screening based on quenched-luminescence oxygen sensing

被引:41
作者
Alderman, J
Hynes, J
Floyd, SM
Krüger, J
O'Connor, R
Papkovsky, DB [1 ]
机构
[1] Natl Microelect Res Ctr, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Dept Biochem, Cork, Ireland
[3] Luxcel Biosci Inc, Dublin 6W, Ireland
关键词
optical oxygen sensing; cell-based assays; oxygen respiration; phosphorescent oxygen probes; cell viability; high throughput screening;
D O I
10.1016/j.bios.2003.12.008
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cell viability assays represent an important technology in modern cell biology, drug discovery and biotechnology, where currently there is a high demand for simple, sensitive and cost-effective screening methods. We have developed a new methodology and associated tools for cell-based screening assays, which are based on the measurement of the rates of oxygen uptake in cells by luminescence quenching. Scalable microchamber devices matching the footprint of a standard 96-well plate were developed and used in conjunction with long-decay phosphorescent oxygen probes. These devices permit cell non-invasive, real-time monitoring of cellular respiration and a rapid, one-step, kinetic assessment of multiple samples for cell viability, drug/effector action. These assays can be carried out on conventional fluorescence plate readers, they are suitable for different types of cells, including adherent and slow-respiring cells, require small sample volumes and cell numbers, and are amenable for high throughput screening. Monitoring of as little as 300 mammalian cells in 3 mul volume has been demonstrated. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1529 / 1535
页数:7
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