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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
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Kinetic Screening of Nuclease Activity using Nucleic Acid Probes
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Screening of DNA-Encoded Small Molecule Libraries inside a Living Cell.

Lars K Petersen1, Allan B Christensen1, Jacob Andersen1

  • 1Vipergen ApS, Gammel Kongevej 23A, DK-1610 Copenhagen V, Denmark.

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|February 12, 2021
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Summary

Researchers developed a novel method for DNA-encoded small molecule library (DEL) screening within living cells using Xenopus laevis oocytes. This breakthrough enables in vivo screening, identifying potent modulators for therapeutic targets like p38α.

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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Drug Discovery

Background:

  • DNA-encoded small molecule libraries (DELs) are powerful tools for identifying novel therapeutic protein modulators.
  • In vivo screening of DELs has been limited by challenges in delivering libraries across cell membranes.

Purpose of the Study:

  • To report the first successful screening of a multimillion-member DEL inside a living cell.
  • To establish a novel method for in vivo DEL screening using Xenopus laevis oocytes.

Main Methods:

  • Utilized large Xenopus laevis oocytes (1 μL) for direct DEL injection, overcoming cell membrane delivery issues.
  • Expressed target proteins fused to a prey protein within oocytes for specific DNA labeling and discrimination.
  • Screened a 194-million-member DEL against p38α, ACSS2, and DOCK5 protein targets.

Main Results:

  • Successfully performed in vivo DEL screening in living cells.
  • Identified multiple chemical clusters for all three tested targets (p38α, ACSS2, DOCK5).
  • Achieved validated hits with single-digit nanomolar potencies for the p38α target.

Conclusions:

  • Demonstrated a powerful new approach for DEL screening in a physiological context.
  • Eliminated the need for highly purified target proteins, simplifying the screening process.
  • Poised to expand the range of DEL-amenable targets and reduce drug candidate attrition rates.