Journal of the American Chemical Society · 2003 · 62 citations · 11 references
PharmacyBiotechnologyMolecular BiologyCombinatorial ChemistryDrug DiscoverySynthetic BiologyBinding SpecificityChemical Library DesignHigh-throughput SynthesisLibrary ConstructionLigand BindingSmall-molecule ScreeningDna-templated SynthesisEnrichmentIn Vitro SelectionProtein Binding AffinitySmall-molecule Library ConstructionSmall-molecule Library DesignSynthetic Dna Library Construction
We have developed in vitro selections for DNA-linked synthetic small molecules with protein binding affinity and specificity. These selections require only generally accessible equipment, offer high degrees of enrichment of active molecules from mixtures of predominantly inactive species, can be applied to a variety of unrelated proteins, and require approximately 108-fold less material than existing synthetic molecule screening methods. Iterating these selections multiplies the net enrichment of active molecules, enabling enormous overall enrichment factors exceeding 106 to be achieved. Further, the selections can be adapted to select for binding specificity in addition to binding affinity. The application of methods described in this work may play a key role in the discovery of desired molecules from DNA-templated synthetic libraries.
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Use of isogenic human cancer cells for high-throughput screening and drug discovery
C Torrance, Vijai Agrawal, Bert Vogelstein et al. · Nature Biotechnology · 2001 · 234 citations
Medicine, Cell Biology, Oncology +12
Magnetic Sensors for Protease Assays
Ming Zhao, Lee Josephson, Yi Tang et al. · Angewandte Chemie International Edition · 2003 · 222 citations · Full text