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- W2332075901 abstract "Identifying druggable targets and their corresponding therapeutic agents are two fundamental challenges in drug discovery research. The one-bead-one-compound (OBOC) combinatorial library method has been developed to discover peptides or small molecules that bind to a specific target protein or elicit a specific cellular response. The phage display cDNA expression proteome library method has been employed to identify target proteins that interact with specific compounds. Here, we combined these two high-throughput approaches, efficiently interrogated approximately 10(13) possible molecular interactions, and identified 91 small molecule compound beads that interacted strongly with the phage library. Of 19 compounds resynthesized, 4 were cytotoxic against cancer cells; one of these compounds was found to interact with EIF5B and inhibit protein translation. As more binding pairs are confirmed and evaluated, the library-against-library screening approach and the resulting small molecule-protein domain interaction database may serve as a valuable tool for basic research and drug development." @default.
- W2332075901 created "2016-06-24" @default.
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- W2332075901 date "2016-05-03" @default.
- W2332075901 modified "2023-10-17" @default.
- W2332075901 title "Rapid Discovery of Functional Small Molecule Ligands against Proteomic Targets through Library-Against-Library Screening" @default.
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- W2332075901 doi "https://doi.org/10.1021/acscombsci.5b00194" @default.
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