| Literature DB >> 24285637 |
Lin Du1, Andrew J Robles, Jarrod B King, Douglas R Powell, Andrew N Miller, Susan L Mooberry, Robert H Cichewicz.
Abstract
A fundamental component for success in drug discovery is the ability to assemble and screen compounds that encompass a broad swath of biologically relevant chemical-diversity space. Achieving this goal in a natural-products-based setting requires access to a wide range of biologically diverse specimens. For this reason, we introduced a crowdsourcing program in which citizen scientists furnish soil samples from which new microbial isolates are procured. Illustrating the strength of this approach, we obtained a unique fungal metabolite, maximiscin, from a crowdsourced Alaskan soil sample. Maximiscin, which exhibits a putative combination of polyketide synthase (PKS), non-ribosomal peptide synthetase (NRPS), and shikimate pathway components, was identified as an inhibitor of UACC-62 melanoma cells (LC50=0.93 μM). The metabolite also exhibited efficacy in a xenograft mouse model. These results underscore the value of building cooperative relationships between research teams and citizen scientists to enrich drug discovery efforts.Entities:
Keywords: antitumor agents; biosynthesis; crowdsourcing; drug discovery; epigenetics
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Year: 2013 PMID: 24285637 PMCID: PMC4028707 DOI: 10.1002/anie.201306549
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336