Abstract
We report the selection of DNA-encoded small molecule libraries against protein targets within the cytosol and on the surface of live cells. The approach relies on generation of a covalent linkage of the DNA to protein targets by affinity labeling. This cross-linking event enables subsequent copurification by a tag on the recombinant protein. To access targets within cells, a cyclic cell-penetrating peptide is appended to DNA-encoded libraries for delivery across the cell membrane. As this approach assesses binding of DELs to targets in live cells, it provides a strategy for selection of DELs against challenging targets that cannot be expressed and purified as active.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Cell-Penetrating Peptides / chemistry*
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Cell-Penetrating Peptides / metabolism
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Cross-Linking Reagents / chemistry
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Cytosol / drug effects
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Cytosol / metabolism
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DNA / chemistry
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Fluoresceins / chemistry
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HEK293 Cells
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Humans
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Lipids
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Peptides, Cyclic / chemistry
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Polymerase Chain Reaction
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Proteins / genetics*
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Proteins / metabolism*
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / metabolism
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Small Molecule Libraries / chemistry
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Small Molecule Libraries / pharmacology*
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Tetrahydrofolate Dehydrogenase / genetics
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Transfection
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Trimethoprim / pharmacology
Substances
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Cell-Penetrating Peptides
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Cross-Linking Reagents
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Fluoresceins
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Lipids
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Lipofectamine
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Peptides, Cyclic
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Proteins
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Recombinant Fusion Proteins
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Small Molecule Libraries
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6-carboxyfluorescein
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DNA
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Trimethoprim
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Tetrahydrofolate Dehydrogenase