Development and Optimization of a Novel 384-Well Anti-Malarial Imaging Assay Validated for High-Throughput Screening

被引:130
作者
Duffy, Sandra [1 ]
Avery, Vicky M. [1 ]
机构
[1] Griffith Univ, Eskitis Inst Cell & Mol Therapies, Nathan, Qld 4111, Australia
关键词
LINKED-IMMUNOSORBENT-ASSAY; PLASMODIUM-FALCIPARUM; DRUG-SENSITIVITY; IN-VITRO; MICROFLUORIMETRIC METHOD; LACTATE-DEHYDROGENASE; MALARIA PARASITES; SUSCEPTIBILITY; CULTURES;
D O I
10.4269/ajtmh.2012.11-0302
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
With the increasing occurrence of drug resistance in the malaria parasite, Plasmodium falciparum, there is a great need for new and novel anti-malarial drugs. We have developed a 384-well, high-throughput imaging assay for the detection of new anti-malarial compounds, which was initially validated by screening a marine natural product library, and subsequently used to screen more than 3 million data points from a variety of compound sources. Founded on another fluorescence-based P falciparum growth inhibition assay, the DNA-intercalating dye 4',6-diamidino-2-phenylindole, was used to monitor changes in parasite number. Fluorescent images were acquired on the PerkinElmer Opera High Throughput confocal imaging system and analyzed with a spot detection algorithm using the Acapella data processing software. Further optimization of this assay sought to increase throughput, assay stability, and compatibility with our high-throughput screening equipment platforms. The assay typically yielded Z'-factor values of 0.5-0.6, with signal-to-noise ratios of 12.
引用
收藏
页码:84 / 92
页数:9
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