Abstract
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. Copyright © 2012 by The American Society of Tropical Medicine and Hygiene.
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CITATION STYLE
Duffy, S., & Avery, V. M. (2012). Development and optimization of a novel 384-well anti-malarial imaging assay validated for high-throughput screening. American Journal of Tropical Medicine and Hygiene, 86(1), 84–92. https://doi.org/10.4269/ajtmh.2012.11-0302
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