Selection of DNA-Encoded Libraries to Protein Targets within and on Living Cells

J Am Chem Soc. 2019 Oct 30;141(43):17057-17061. doi: 10.1021/jacs.9b08085. Epub 2019 Oct 22.

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

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell-Penetrating Peptides / chemistry*
  • Cell-Penetrating Peptides / metabolism
  • Cross-Linking Reagents / chemistry
  • Cytosol / drug effects
  • Cytosol / metabolism
  • DNA / chemistry
  • Fluoresceins / chemistry
  • HEK293 Cells
  • Humans
  • Lipids
  • Peptides, Cyclic / chemistry
  • Polymerase Chain Reaction
  • Proteins / genetics*
  • Proteins / metabolism*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Small Molecule Libraries / chemistry
  • Small Molecule Libraries / pharmacology*
  • Tetrahydrofolate Dehydrogenase / genetics
  • Transfection
  • Trimethoprim / pharmacology

Substances

  • Cell-Penetrating Peptides
  • Cross-Linking Reagents
  • Fluoresceins
  • Lipids
  • Lipofectamine
  • Peptides, Cyclic
  • Proteins
  • Recombinant Fusion Proteins
  • Small Molecule Libraries
  • 6-carboxyfluorescein
  • DNA
  • Trimethoprim
  • Tetrahydrofolate Dehydrogenase