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Open Access Highly Accessed Methodology article

High-content live cell imaging with RNA probes: advancements in high-throughput antimalarial drug discovery

Serena Cervantes1, Jacques Prudhomme2, David Carter3, Krishna G Gopi4, Qian Li6, Young-Tae Chang45 and Karine G Le Roch2*

Author affiliations

1 Cell, Molecular, and Developmental Biology Graduate Program, University of California, Riverside, CA, 92521, USA

2 Department of Cell Biology and Neurosciences, University of California, Riverside, CA, 92521, USA

3 Institute for Integrative Genome Biology, University of California, Riverside, CA, 92521, USA

4 Department of Chemistry, & NUS MedChem Program of the Office of Life Sciences, National University of Singapore, 11754, Singapore

5 Laboratory of Bioimaging Probe Development, Singapore Bioimaging Consortium, Agency for Science, Technology and Research (A*STAR), Biopolis, 138667, Singapore

6 Department of Chemistry, New York University, New York, NY 10003, USA

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Citation and License

BMC Cell Biology 2009, 10:45  doi:10.1186/1471-2121-10-45

Published: 10 June 2009

Abstract

Background

Malaria, a major public health issue in developing nations, is responsible for more than one million deaths a year. The most lethal species, Plasmodium falciparum, causes up to 90% of fatalities. Drug resistant strains to common therapies have emerged worldwide and recent artemisinin-based combination therapy failures hasten the need for new antimalarial drugs. Discovering novel compounds to be used as antimalarials is expedited by the use of a high-throughput screen (HTS) to detect parasite growth and proliferation. Fluorescent dyes that bind to DNA have replaced expensive traditional radioisotope incorporation for HTS growth assays, but do not give additional information regarding the parasite stage affected by the drug and a better indication of the drug's mode of action. Live cell imaging with RNA dyes, which correlates with cell growth and proliferation, has been limited by the availability of successful commercial dyes.

Results

After screening a library of newly synthesized stryrl dyes, we discovered three RNA binding dyes that provide morphological details of live parasites. Utilizing an inverted confocal imaging platform, live cell imaging of parasites increases parasite detection, improves the spatial and temporal resolution of the parasite under drug treatments, and can resolve morphological changes in individual cells.

Conclusion

This simple one-step technique is suitable for automation in a microplate format for novel antimalarial compound HTS. We have developed a new P. falciparum RNA high-content imaging growth inhibition assay that is robust with time and energy efficiency.