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High-content screening in infectious diseases
Authors:Brodin Priscille  Christophe Thierry
Affiliation:1Biology of Intracellular Pathogens Inserm Avenir Team, Republic of Korea;2Screening Technologies and Pharmacology, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do 463-440, Republic of Korea;3Chemical Genomics of Intracellular Mycobacteria, Inserm U1019, CNRS UMR8204, Institut Pasteur of Lille, Center for Infection and Immunity of Lille, University of Lille - North of France, 1, rue du professeur Calmette, BP245, 59019 Lille Cedex, France
Abstract:The last decade has seen the development of automated microscopy and its adaptation for various areas of research, particularly infectious disease. Most of the high-content screening (HCS) platforms now integrate all of the following necessary steps: automated pipettes for assay miniaturization in 384-well plates, automated image acquisition and data storage and analysis. HCS was initially associated with RNA interference genetic screens for identifying host factors involved in host-pathogen interactions. More recently, both in academia and in industry, HCS has been adapted for drug discovery purposes. High-content analysis enables intracellular tracking of viral particles to profile the antiviral mechanisms of each compound. Adaptation to high-throughput screening in bacteriology and parasitology has already led to the discovery of new types of host-specific inhibitors that differ from those inhibitors that act directly on microbes.
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