Proceedings of the National Academy of Sciences · 1992 · 1K citations · 9 references
PharmacyGeneticsMedicinal ChemistryCombinatorial ChemistryDrug DesignDrug DiscoveryCombinatorial SynthesisHigh-throughput ScreeningLibrary ConstructionLibrary DesignLibrary ScreeningParallel SynthesisChemical Library SynthesisCombinatorial Library ConstructionCombinatorial Library DesignCombinatorial Library ScreeningCombinatorial Library SynthesisDrug ScreeningEncoded Combinatorial LibrariesLibrary Encoding
The diversity of chemical synthesis and the power of genetics are linked to provide a powerful, versatile method for drug screening. A process of alternating parallel combinatorial synthesis is used to encode individual members of a large library of chemicals with unique nucleotide sequences. After the chemical entity is bound to a target, the genetic tag can be amplified by replication and utilized for enrichment of the bound molecules by serial hybridization to a subset of the library. The nature of the chemical structure bound to the receptor is decoded by sequencing the nucleotide tag.
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In vitro selection of RNA molecules that bind specific ligands
Andrew D. Ellington, Jack W. Szostak · Nature · 1990 · 9.7K citations
Light-Directed, Spatially Addressable Parallel Chemical Synthesis
Stephen P. A. Fodor, Jill Read, Michael C. Pirrung et al. · Science · 1991 · 2.7K citations
Searching for Peptide Ligands with an Epitope Library
Jamie K. Scott, George P. Smith · Science · 1990 · 2.1K citations
A new type of synthetic peptide library for identifying ligand-binding activity
Kit S. Lam, Sydney E. Salmon, Evan M. Hersh et al. · Nature · 1991 · 1.8K citations