Efficient discovery of anti-inflammatory small-molecule combinations using evolutionary computing

Ben G. Small, Barry W. McColl, Richard Allmendinger, Jorgen Pahle, Gloria Lopez-Casteon, Nancy J. Rothwell, Joshua Knowles, Pedro Mendes, David Brough, Douglas B. Kell

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The control of biochemical fluxes is distributed, and to perturb complex intracellular networks effectively it is often necessary to modulate several steps simultaneously. However, the number of possible permutations leads to a combinatorial explosion in the number of experiments that would have to be performed in a complete analysis. We used a multiobjective evolutionary algorithm to optimize reagent combinations from a dynamic chemical library of 33 compounds with established or predicted targets in the regulatory network controlling IL-1 2 expression. The evolutionary algorithm converged on excellent solutions within 11 generations, during which we studied just 550 combinations out of the potential search space of ĝ̂1/49 billion. The top five reagents with the greatest contribution to combinatorial effects throughout the evolutionary algorithm were then optimized pairwise. A p38 MAPK inhibitor together with either an inhibitor of I °B kinase or a chelator of poorly liganded iron yielded synergistic inhibition of macrophage IL-1 2 expression. Evolutionary searches provide a powerful and general approach to the discovery of new combinations of pharmacological agents with therapeutic indices potentially greater than those of single drugs. © 2011 Nature America, Inc. All rights reserved.
Original languageEnglish
Pages (from-to)902-908
Number of pages6
JournalNature chemical biology
Issue number12
Publication statusPublished - Dec 2011

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