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Cheaper faster drug development validated by the repositioning of drugs against neglected tropical diseases
Author(s) -
Kevin Williams,
Elizabeth Bilsland,
Andrew C. Sparkes,
Wayne Aubrey,
Michael J. Young,
Larisa Soldatova,
Kurt De Grave,
Jan Ramon,
Michaela de Clare,
Worachart Sirawaraporn,
Stephen G. Oliver,
Ross D. King
Publication year - 2015
Publication title -
journal of the royal society interface
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 139
eISSN - 1742-5689
pISSN - 1742-5662
DOI - 10.1098/rsif.2014.1289
Subject(s) - drug discovery , malaria , automation , computer science , drug , drug development , neglected tropical diseases , risk analysis (engineering) , artificial intelligence , computational biology , data science , biology , microbiology and biotechnology , pharmacology , bioinformatics , medicine , engineering , immunology , mechanical engineering , disease , pathology
There is an urgent need to make drug discovery cheaper and faster. This will enable the development of treatments for diseases currently neglected for economic reasons, such as tropical and orphan diseases, and generally increase the supply of new drugs. Here, we report the Robot Scientist ‘Eve’ designed to make drug discovery more economical. A Robot Scientist is a laboratory automation system that uses artificial intelligence (AI) techniques to discover scientific knowledge through cycles of experimentation. Eve integrates and automates library-screening, hit-confirmation, and lead generation through cycles of quantitative structure activity relationship learning and testing. Using econometric modelling we demonstrate that the use of AI to select compounds economically outperforms standard drug screening. For further efficiency Eve uses a standardized form of assay to compute Boolean functions of compound properties. These assays can be quickly and cheaply engineered using synthetic biology, enabling more targets to be assayed for a given budget. Eve has repositioned several drugs against specific targets in parasites that cause tropical diseases. One validated discovery is that the anti-cancer compound TNP-470 is a potent inhibitor of dihydrofolate reductase from the malaria-causing parasite Plasmodium vivax .

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